Small Cell Lung Cancer* George R. Simon, MD, FCCP; and Henry Wagner, MD
Among patients with lung cancers, the proportion of those with small cell lung cancer (SCLC) has decreased over the last decade. SCLC is staged as limited-stage disease and extensive-stage disease. Standard staging procedures for SCLC include CT scans of the chest and abdomen, bone scan, and CT scan or MRI of the brain. The role for positron emission tomography scanning in the staging of SCLC has yet to be defined. Limited-stage disease is treated with curative intent with chemotherapy and radiation therapy, with approximately 20% of patients achieving a cure. The median survival time for patients with limited-stage disease is approximately 18 months. Extensive-stage disease is treated primarily with chemotherapy, with a high initial response rate of 60 to 70% and a complete response rate of 20 to 30%, but with a median survival time of approximately 9 months. Patients achieving a complete remission should be offered prophylactic cranial irradiation. Currently, there is no role for maintenance treatment or bone marrow transplantation in the treatment of patients with SCLC. Relapsed or refractory SCLC has a uniformly poor prognosis. In this section, evidence-based guidelines for the staging and treatment of SCLC are outlined. (CHEST 2003; 123:259S–271S) Key words: carboplatin; chemotherapy; cisplatin; etoposide; irinotecan; paclitaxel; prophylactic cranial irradiation; radiation therapy; small cell lung cancer Abbreviations: CAV ⫽ cyclophosphamide, adriamycin, and vincristine; CODE ⫽ cyclophosphamide, vincristine, doxorubicin, and etoposide; CR ⫽ complete response; ECOG ⫽ Eastern Cooperative Oncology Group; G-CSF ⫽ granulocyte colony-stimulating factor; NSCLC ⫽ non-small cell lung cancer; PCI ⫽ prophylactic cranial irradiation; PET ⫽ positron emission tomography; SCLC ⫽ small cell lung cancer; TEP ⫽ paclitaxel, etoposide, and cisplatin; TRT ⫽ thoracic radiotherapy
is the result of a comprehensive T hisreviewdocument of the existing guidelines, meta-analyses, and relevant randomized clinical trials on the subject of small cell lung cancer (SCLC). Among lung cancers, the proportion of patients with SCLC has decreased from 17.4% in 1986 to 13.8% in 1998.1 Like non-SCLC (NSCLC), it has a strong association with tobacco use, but its clinical characteristics tend to be more aggressive than NSCLC, and median survival time without treatment is between 2 and 4 months. Staging of SCLC Patients are staged according to a two-stage system, which was developed by the Veterans Administration Lung Cancer Study Group, as having limitedstage disease or extensive-stage disease. Patients with limited-stage disease have involvement restricted to the ipsilateral hemithorax within a single *From the H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL. Correspondence to: George R. Simon, MD, FCCP, 12902 Magnolia Dr, Suite 3170, Thoracic Oncology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612; e-mail:
[email protected] www.chestjournal.org
radiation port. Extensive-stage disease is defined as the presence of obvious metastatic disease. Patients with limited-stage disease with the presence of contralateral hilar and/or supraclavicular nodes and/or with malignant pericardial and/or pleural effusions are excluded from clinical trials for limited-stage SCLC. A complete evaluation of a patient newly diagnosed with SCLC should consist of a medical history and physical examination, a review of the histopathology specimens, a CT scan of the chest and upper abdomen to include the whole liver and the adrenal glands, a bone scan, and a CT scan or MRI examination of the brain. Additionally, complete blood counts, measurement of electrolyte, BUN, and creatinine levels, liver function tests, and measurement of lactate dehydrogenase levels should be performed in all patients at baseline. The utility of positron emission tomography (PET) scanning in patients with SCLC has been recently reported in two small prospective studies.2,3 In a study reported by Hauber et al,2 PET scans detected all primary lesions, lymph node metastases, and distant metastases that had been detected by other standard staging procedures. In a second study,3 30 patients with SCLC were evaluated with 36 PET scan examinations, and the CHEST / 123 / 1 / JANUARY, 2003 SUPPLEMENT
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results were compared with the sum of the other staging procedures. The results of 23 of the 36 PET scan examinations were concordant with those of the other staging procedures. In seven cases, the PET scan examination resulted in upward staging of the patient, and in one instance the PET scan revealed the presence of a viable tumor when conventional staging procedures had revealed no residual disease. PET scan identified all areas of tumor involvement detected by other staging procedures. A third study102 looked at the accuracy of PET scanning in detecting bony metastases in patients with SCLC and NSCLC, comparing the PET scans to bone scans and single-photon emission CT scans. In this study, PET scans were found to be the most accurate whole-body imaging modality for the screening of bone metastases. These studies suggested that PET scanning is likely to be a useful staging tool in patients with SCLC. However, all the above studies were small, and the experience with PET scan as a staging tool remains largely limited. Until larger prospective studies become available, PET scanning cannot be recommended for routine use in the staging and restaging of patients with SCLC. Recommendation 1. In all patients, the routine staging of SCLC should include medical history and physical examination, complete blood counts, comprehensive chemistry panels, CT scans of the chest and abdomen, a CT scan or MRI of the brain, and a bone scan. Level of evidence, good; benefit, substantial; grade of recommendation, A 2. For the routine staging of patients with SCLC, PET scanning is not recommended outside of a clinical trial. Level of evidence, fair; benefit, none/negative; grade of recommendation, D
Treatment of Extensive Stage SCLC First-Line Treatment Platinum-based chemotherapy remains the mainstay of treatment for extensive SCLC. In a metaanalysis4 of randomized trials (19 trials and 4,054 evaluable patients) comparing a cisplatin-based regimen with a non-cisplatin-based regimen, patients randomized to a regimen containing cisplatin had a significant increase in the probability of response and survival with no significant increase in toxicity. Detailed analyses of the roles of etoposide and cisplatin in the treatment of SCLC have been performed by Berghmans et al5 and were reported in abstract form in September 1999. Thirty-six eligible trials that were performed between 1980 and 1998 were clas260S
sified into the following four groups: (1) cisplatin vs no cisplatin (1 trial); (2) etoposide (without cisplatin) vs no etoposide (17 trials); (3) cisplatin/etoposide vs no cisplatin/etoposide (9 trials); and (4) cisplatin/ etoposide vs etoposide (9 trials). The authors concluded that the use of cisplatin and/or etoposide offered a significant survival advantage to patients with SCLC.5 In another meta-analysis, Chute et al6 evaluated all 21 cooperative group trials performed in North America from 1972 to 1993. Patients with extensivestage SCLC who were treated during a similar time interval and were listed in the Surveillance, Epidemiology, and End Results database also were examined. Trends were tested in the number of trials and the survival of patients over time. In this analysis, a modest 2-month prolongation in median survival was demonstrated in patients with extensive-stage SCLC. This improvement in survival was independently associated with both cisplatin-based therapy and in the improvement of best supportive care. This metaanalysis again establishes that cisplatin-based chemotherapy should be the cornerstone of first-line chemotherapy for patients with extensive-stage SCLC. The issue of carboplatin vs cisplatin was recently reviewed by Brahmer and Ettinger,7 who concluded that carboplatin plus etoposide is as effective as cisplatin plus etoposide but is less toxic (except for increased myelosuppression). The Hellenic Oncology Group conducted a phase III trial103 comparing cisplatin and etoposide with carboplatin and etoposide. In this study, containing patients with both limited-stage and extensive-stage disease, the median survival time was 11.8 months for cisplatin plus etoposide and 12.5 months for carboplatin plus etoposide. The difference was not statistically significant, although the study was not powered to show equivalence.103 A recent Japanese trial8 compared cisplatin and irinotecan with cisplatin and etoposide. Patients randomized to the cisplatin/irinotecan arm did (statistically) significantly better than the group that was randomized to the cisplatin/etoposide arm (median survival time, 420 vs 300 days, respectively). Confirmatory trials are underway in the United States. Several phase II trials with irinotecan, topotecan, and paclitaxel in combination with either cisplatin or etoposide have been reported, and these have been summarized in Table 1. The issue of adding a third drug to cisplatin and etoposide has been investigated. The Hoosier Oncology Group evaluated the addition of ifosfamide to cisplatin and etoposide in a phase III trial of 171 patients with extensive-stage disease. At the expense of increased toxicity, the 2-year survival rate increased from 5 to 13% with the addition of ifosLung Cancer Guidelines
Table 1—Phase II Trials of SCLC Patients Receiving Combination Chemotherapy vs Untreated Patients* Responders, No. Treatment CEC TEP TEP Cisplatin-irinotecan Cisplatin-vinblastine-MMC Cisplatin-etoposide-all-trans-RA Cisplatin-paclitaxel-G-CSF Topotecan-paclitaxel Etoposide-irinotecan Paclitaxel-carboplatin Paclitaxel-irinotecan Paclitaxel-doxorubicin Cisplatin-docetaxel Topotecan-paclitaxel Topotecan-paclitaxel CPT EPE
Patients, No. 46 38 23 35 30 22 34 28 50 69 11 16 20 13 15 18 12
Response Rate
Survival†
CR
PR
Total
%
95% CL
Mo
10 6 5 10 1 1 3 6
32 28 14 20 21 9 20 11
5 4 1 0
37 1 3 11 5 10 6
91 90 83 86 73 45 61 60 66 61 45 25 55 69 100 72 100
79–98 75–97 61–95 70–95 66–96 24–68 53–8 41–79 51–79 48–72 17–77 7–52 32–77 39–91 78–100 47–90 74–100
18‡ 12 11 13 6 11 8 14 12 12
10 3 6
42 34 19 30 22 10 23 17 33 42 5 4 11 8 15 13 12
1-Yr Rate, %
Reference
22 46 21.7 41
14
69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85
*CEC ⫽ cisplatin-etoposide-carboplatin; MMC ⫽ mitomycin C; RA ⫽ retinoic acid; CL ⫽ confidence limits; CPT ⫽ cisplatin-paclitaxel-topotecan; EPE ⫽ etoposide-paclitaxel-epirubicin; PR ⫽ partial response. †Values given as median. ‡Includes 14 patients with stage IIIB and stage IV disease.
famide.9 Mavroudis et al10 compared the use of paclitaxel, etoposide, and platinum (TEP) with the use of etoposide and platinum. The study was terminated early, secondary to a higher number of toxic deaths in the TEP arm. Despite a statistically significant improvement in the time to progression for TEP, there was no difference in overall survival. Recently, another phase III intergroup trial (Cancer and Leukemia Group B 9732) was reported11 comparing cisplatin and etoposide with or without paclitaxel in patients with extensive-stage SCLC. No significant survival advantage was seen with the addition of paclitaxel to cisplatin and etoposide in this study. On the other hand, there was an increased incidence of deaths from toxicities in the paclitaxel arm. Recommendations 3. Patients with extensive-stage disease should receive platinum-based chemotherapy. Level of evidence, good; benefit, substantial; grade of recommendation, A 4. Patients achieving a complete remission (CR) should be offered prophylactic cranial irradiation (PCI). Level of evidence, fair; benefit, small; grade of recommendation, C
Lung Cancer in 1998.12 Several randomized trials have demonstrated that 4 to 6 months of treatment is equal to prolonged treatment when survival is considered as the end point. In the meta-analysis reported by Sculier et al,12 13 published randomized trials were included. One showed a statistically significant difference in survival in favor of maintenance therapy, 5 studies showed survival advantage in subgroups of patients, 1 study showed significantly shorter survival times with maintenance therapy, and 6 studies showed no difference. The Eastern Cooperative Oncology Group (ECOG) conducted a phase III trial in which patients showing a response to therapy or patients whose disease stabilized after receiving four cycles of cisplatin and etoposide were randomized to observation alone or to four cycles of topotecan therapy.13 Despite an improvement in progression-free survival, there was no difference in overall survival between the two groups. Treatments other than chemotherapy for maintenance are currently being investigated in ongoing clinical trials. A phase III randomized trial is currently underway testing the efficacy of anti-GD3 immunization as maintenance treatment. Metalloproteinase inhibitors and inhibitors of angiogenesis also are being investigated in this fashion. Recommendation
Maintenance Treatment The topic of maintenance therapy in patients with SCLC was extensively reviewed in the journal www.chestjournal.org
5. For patients with extensive-stage or limitedstage SCLC achieving a partial or CR, there is no evidence, outside of a clinical trial, for CHEST / 123 / 1 / JANUARY, 2003 SUPPLEMENT
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maintenance treatment. Level of evidence, good; benefit, none/negative; grade of recommendation, D Treatment of Relapsed or Refractory SCLC Despite high initial response rates to chemotherapy (ie, 45 to 75% CRs) reported in patients with limited-stage disease and 20 to 30% CRs in patients with extensive-stage disease, the response duration is usually short with a progression-free survival time of approximately 4 months for patients with extensivestage disease and 12 months for patients with limitedstage disease. Most patients are destined to relapse, and the prognosis of this group of relapsed patients is poor. Patients who relapse ⬍ 3 months after firstline therapy are commonly called refractory, and patients who relapse 3 months after therapy are called sensitive. Patients with late relapses after receiving initial therapy may be retreated with the same induction regimen used initially. Patients whose disease progresses early after induction therapy and who are in satisfactory clinical condition, should be offered a second-line regimen. In a randomized multicenter study, von Pawel et al101 compared cyclophosphamide, adriamycin, and vincristine (CAV) with topotecan as a single agent in patients who relapsed at least 60 days after the completion of initial therapy. A total of 211 patients were enrolled in the study. The response rate was 24.3% in patients who were treated with topotecan and was 18.3% in patients treated with CAV (p ⫽ 0.285). The median times to disease progression were 13.3 weeks for patients in the topotecan arm and 12.3 weeks for patients in the CAV arm. The median survival time was 25 weeks for patients receiving topotecan and 24.7 weeks for those receiving CAV. The proportion of patients who experienced symptom improvement was greater in the topotecan arm than
in the CAV group for four of the eight symptoms evaluated. The authors concluded that topotecan was at least as effective as CAV in the treatment of patients with recurrent SCLC and resulted in improved control of several symptoms. However, toxicity rates were high in both arms of the study, and alternative dose schedules of topotecan are currently being evaluated. Several recently reported phase II trials in patients with relapsed/ refractory SCLC are summarized in Table 2. Recommendation 6. Patients with SCLC who have relapsed following an initial response to treatment or who are refractory to the initial treatment should be offered further chemotherapy. The chemotherapy offered will depend on the duration of response after receiving first-line chemotherapy or the lack of response to first-line chemotherapy (ie, sensitive relapses vs refractory patients). Level of evidence, fair; benefit, small/ weak; grade of recommendation, C
Treatment of Elderly Patients With Extensive-Stage SCLC Approximately 25% of patients with SCLC are ⬎ 70 years of age (ie, elderly). The performance status and the physiologic status of the patient should guide treatment decisions rather than the patient’s chronologic age. It is clear that patients with good performance status (ECOG level 0 or 1) and normal organ function should be treated with optimal chemotherapy (and with radiotherapy, if indicated) as in their younger counterparts. Similar outcomes of elderly patients with limited-stage SCLC have been shown in the intergroup trial 0096 in which cisplatin, etoposide, and thoracic radiotherapy were administered once a day or twice daily.14 The National Cancer Institute of Canada performed a retrospec-
Table 2—Phase II Trials of SCLC Patients Receiving Combination Chemotherapy: Refractory or Relapsed Patients* Responders, No.
Survival†
Treatment
Patients, No.
CR
PR
Total
Response Rate, %
Etoposide-irinotecan Cisplatin-topotecan Etoposide-hexmethylmelamine Irinotecan-paclitaxel Carboplatin-paclitaxel
24 28 30 11 18
3 1 1 1 0
14 7 5 4 3
17 8 6 5 3
71 29 22 45 17
Mo
1 Yr Rate, %
9 5
21
Reference 86 87 88 89 90
*See Table 1 for abbreviations not used in the text. †Values given as median. 262S
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tive review15 of their BR3 and BR6 trials and also concluded that age did not appear to impact the delivery, tolerance, or efficacy of thoracic irradiation in the combined-modality management of patients with limited-stage SCLC. Greater myelosuppression is to be expected since equivalent exposure to a drug will lead to more myelosuppression in the elderly compared to their younger counterparts. This has been shown to be the case at least for etoposide.16 Greater ancillary support will be required in the elderly. However, despite treatment delays elderly patients with good performance status have similar prognoses to those of younger patients. Elderly patients with poor performance status or with compromised organ function may be offered single-agent chemotherapy or polychemotherapy in attenuated doses. However, several randomized studies17,18 have indicated that such “gentler” chemotherapy is inferior to optimal combination chemotherapy. Options available to these patients include the following: oral etoposide for 14 days combined with carboplatin on day 1 every 28 days19; abbreviated chemotherapy with CAV in full doses followed 3 weeks later by chemotherapy with cisplatin and etoposide in optimal doses20; or chemotherapy with platinum, adriamycin, vincristine, and etoposide in reduced doses.21 A recently reported phase III trial22 compared carboplatin-gemcitabine therapy with cisplatin-etoposide therapy in patients with SCLC who had poor prognoses, with carboplatin-gemcitabine therapy exhibiting a more favorable overall toxicity profile at the expense of increased myelotoxicity. Another phase III trial compared the use of single-agent carboplatin with CAV,23 with carboplatin producing response rates, relief of tumor-related symptoms, and survival similar to that seen with CAV. There was a lower risk of life-threatening sepsis and less need for hospitalization in the group that received carboplatin. Recommendations 7. Elderly patients with good performance status and with intact organ function should be treated with platinum-based chemotherapy. Level of evidence, good; benefit, moderate; grade of recommendation, B 8. Elderly patients with poor prognostic factors such as poor performance status or severe concomitant comorbid disease still may be considered for chemotherapy. Level of evidence, poor; benefit, small; grade of recommendation, C 9. Elderly patients achieving a CR should be offered PCI. Level of evidence, fair; benefit, small; grade of recommendation, C www.chestjournal.org
Dose Intensity in SCLC The issue of dose intensity has been subjected to extensive clinical investigation in recent years primarily due to the initially chemosensitive nature of the disease and also owing to the almost universal lack of durable responses and cure, despite the initial responses. Several randomized trials,24 –26 however, have failed to show a survival advantage with doseintense chemotherapy. On the basis of promising results from a pilot trial reported by Murray et al,27 the Southwest Oncology Group reported the results of their phase III trial comparing therapy with cisplatin, vincristine, doxorubicin, and etoposide (CODE) with alternating therapy using CAV then cisplatin and etoposide. The study was stopped early owing to an excessive mortality rate in the CODE arm (8%) compared to the standard arm (1%). The response rates with CODE were higher than that of patients in the standard arm of the study, but progression-free survival and overall survival were not statistically significantly improved. Furuse et al28 and Skarlos et al29 compared more dose-intense weekly regimens with standard or alternating noncross-resistant regimens and again failed to show a survival advantage for the weekly, more dose-intense arms. Pujol et al30 compared therapy with cyclophosphamide, epirubicin, etoposide, and cisplatin in higher doses with recombinant human granulocytemacrophage colony-stimulating factor vs the same drugs in lower doses without granulocyte-macrophage colony-stimulating factor and failed to show a survival advantage for patients in the more doseintense arm. However, Steward et al,31 comparing therapy with the combination of vincristine, ifosfamide, carboplatin, and etoposide every 3 weeks vs the same regimen every 4 weeks, showed a significant survival advantage for patients receiving the intensified regimen. Another trial, which was conducted by Thatcher et al32 and that also showed positive results for the dose-intense approach, compared standard therapy with adriamycin, cyclophosphamide, and etoposide administered every 3 weeks with dose-dense therapy with adriamycin, cyclophosphamide, and etoposide administered every 2 weeks along with granulocyte-colony stimulating factor (GCSF) support. The overall survival rate was statistically significantly better in the dose-dense group (1-year survival rate, 47% vs 39%, respectively [p ⫽ 0.04]; 2-year survival rate, 13% vs 8%, respectively). Progression-free survival, nonhematologic toxicity, and quality of life were similar in the two groups. Interestingly, Arriagada et al33 conducted a randomized trial of 105 patients with limited-stage SCLC who were randomized to receive a higher CHEST / 123 / 1 / JANUARY, 2003 SUPPLEMENT
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dose of cisplatin (100 vs 80 mg/m2) or cyclophosphamide (300 vs 225 mg/m2) initially. All patients then were treated with the same dose of doxorubicin and etoposide, and radiotherapy. There was an improved disease-free survival rate (2-year survival rate, 28% vs 8%, respectively; p ⫽ 0.02) and an improved overall survival rate (2-year survival rate, 46% vs 26%, respectively; p ⫽ 0.02) among patients in the higher dose arm. The issue of dose intensity may need further evaluation in the limited-stage disease setting. Recommendation 10. For patients with either extensive-stage SCLC or limited-stage SCLC, there is no role for dose-dense/intense initial/induction, or maintenance treatment outside of a clinical trial. Level of evidence, good; benefit, none/negative; grade of recommendation, D
The Role of Growth Factor and the Use of Stem Cell Support in SCLC The use of G-CSF in the treatment of SCLC has been analyzed carefully by Chouaid et al.34 They did a retrospective review of their experience and also analyzed published data from three randomized trials that evaluated the effectiveness of primary therapy with G-CSF in patients with SCLC. The use of G-CSF for primary prophylaxis was not found to be cost-effective, did not improve palliation, and hence is not recommended for routine use. Recommendation 11. In patients with SCLC who are receiving chemotherapy, the routine use of G-CSF is not recommended. level of evidence, good; benefit, none/negative; grade of recommendation, D.
Treatment of Limited-Stage SCLC Radiation Therapy in SCLC SCLC has long been recognized to be clinically responsive to radiation, and in vitro radiation of SCLC cell lines has shown that they often have a greater intrinsic radiosensitivity than adenocarcinomas or squamous cell lung cancer cell lines. Because of these observations, many early trials of combining radiation with chemotherapy in patients with SCLC used low total radiation doses. More recently, it has become increasingly clear that higher doses than the 264S
old regimens of 30 Gy in 10 fractions or 45 Gy in 25 fractions are needed to provide durable local control. A number of trials conducted in the 1970s and 1980s compared chemotherapy alone to chemotherapy plus thoracic radiation therapy (TRT) in patients with limited SCLC. These varied in radiation dose, timing, and choice of chemotherapeutic agents (but most were performed with an alkylating agent and doxorubicin-based therapy rather than with cisplatin and etoposide). The analysis by Warde and Payne35 showed improved local control and survival with the addition of TRT, particularly in patients ⬍ 60 years. Pignon et al36 obtained individual patient data from these trials and were able to update analyses from the time of the original publication. They found that the addition of TRT resulted in an increase in the 3-year survival rate from 8.9 to 14.3%, an absolute improvement of 5%, and a relative improvement of nearly 50%.36 With the publication of these two meta-analyses, the debate shifted from whether or not to employ TRT to how best to integrate it with chemotherapy. Sequencing and Timing of Thoracic Radiation and Chemotherapy The issues here are whether to administer radiation therapy and chemotherapy concurrently, sequentially, or in an alternating fashion, and whether radiation should be administered early or late in the overall course of treatment. Murray and Coldman37 performed a meta-analysis of trials that combined chemotherapy and TRT, using progression-free survival at 3 years as a surrogate end point for long-term survival. The best results were seen with TRT beginning 3 to 5 weeks from the start of chemotherapy. As radiation was further delayed, the benefit decreased and survival approached that seen with chemotherapy alone. There have been at least nine randomized trials that have addressed the issue of the timing of radiation in patients with limited-stage SCLC (Table 3). There are major differences in trial design, choice of chemotherapeutic agents, radiation dose, and fractionation schedules. With those caveats, several reasonable conclusions emerge from these data, as follows: 1. Trials that used alkylating agents and doxorubicin-based chemotherapy showed little effect of radiation timing and sequencing. They also reported significant difficulty in delivering planned treatment (both chemotherapy and radiation) when radiation was given concurrently with or alternated between cycles of chemotherapy. Long-term survival in most of Lung Cancer Guidelines
Table 3—Randomized Trials of Radiation-Chemotherapy Sequencing and Timing in Limited-Stage SCLC* Study Perry et al91
Comparison
Chemotherapy
Result
Comment
CAV/CEV
Delayed TRT gave best survival
CAV/PE alternating CAV/PE alternating PE
Median and 4-yr survival favored early TRT Delayed TRT nonsignificantly better (MST, 12.9 vs 10.7 mo) 3-yr survival significantly better for early concurrent vs late sequential (30.9% vs 20.7%, respectively) Nonsignificant trend favoring delayed TRT
Planned drug dose reduction in arm with day 1 TRT Greatest difference in patterns of failure was in CNS relapse No long-term follow-up reported
Murray et al92
TRT day 1 vs day 64 vs none TRT cycle 2 vs cycle 6
Schultz et al93
TRT day 1 vs day 120
Tsukada et al94
TRT concurrent with cycle 1 or following cycle 4
Gregor et al95
TRT alternating between cycles 2, 3, 4, and 5 or following cycle 5 TRT concurrent with cycle 2 or alternating among cycles 2, 3, 4, and 5 TRT starting week 1 vs week 18
CAE
TRT starting week 1 vs week 13 TRT starting week 1 vs week 6
LeBeau et al96
Work et al97
Samantas et al98 Jeremic et al99
Double comparison of timing and concurrency
More toxicity with resultant drug dose reduction and delay in alternating arm
CAE
No difference in median survival
No long-term data; poor compliance in alternating arm
CAV and PE
No difference in median or 5-yr survival
CbpE
No difference in median or 2-yr survival MST significantly better for early TRT (34 vs 26 mo, respectively)
Early RT preceeded chemotherapy and was not concurrent with it Reasonably good 2-year survival rate (35%) Local control better with early TRT
CbpE
*A ⫽ doxorubicin; C ⫽ cyclophosphamide; Cbp ⫽ carboplatin; E ⫽ etoposide; P ⫽ cisplatin; V ⫽ vincristine; MST ⫽ median survival time; RT ⫽ radiation therapy. Table modified and expanded from Wagner.100
these trials was in the range of 10% that is minimally different from that seen with chemotherapy alone. 2. When platinum-etoposide regimens are used for chemotherapy, concurrent chemotherapyTRT is superior to sequential TRT, where TRT is administered after chemotherapy. 3. When platinum-etoposide chemotherapy and concurrent TRT are combined, the data are divergent as to whether early TRT (ie, in week 1) is better than delayed TRT (ie, week 6 or week 13). Radiation Dose Relatively few trials have addressed the issue of optimal TRT dose in patients with SCLC. A retrospective analysis38 of patients treated at the Massachusetts General Hospital showed an improvement in local control as radiation doses were increased from 30 to 50 Gy. The Cancer and Leukemia Group B39 has tried to define the maximal tolerated dose for concurrent TRT and cisplatin-etoposide chemotherapy when these are administered after three courses of induction chemotherapy with cyclophosphamidecisplatin-etoposide. They examined both a once-aday radiation therapy schedule with 2-Gy fractions www.chestjournal.org
and a twice-daily schedule with 1.5-Gy fractions. The limiting toxicity was acute esophagitis, and the maximum tolerated dose was reported to be 45 Gy in 3 weeks for twice-daily fractionation and 70 Gy in 7 weeks for daily fractionation. As the best local control rates in current trials do not exceed 70%, the exploration of dose escalation seems warranted, and a recent trial proposed by the ECOG to the National Cancer Institute would compare the regimen of twice-daily 45-Gy doses for 3 weeks to that of a daily 70-Gy dose for 7 weeks. Studies in patients with NSCLC clearly have shown the feasibility of giving even higher radiation doses to conformal planned fields with concurrent chemotherapy, and this approach may also be feasible in patients with SCLC. Radiation Fractionation The rapid growth of many SCLC cell lines encouraged the exploration of treatment acceleration by giving two fractions per day with a modest reduction in fraction size from the usual 1.8 to 2.0 Gy to 1.5 Gy. Two prospective trials have compared this approach to conventional daily fractionation. The North American Intergroup trial 0096 compared doses of 45 Gy administered in 25 fractions for ⬎ 5 weeks to the investigational arm of doses of 45 Gy administered in CHEST / 123 / 1 / JANUARY, 2003 SUPPLEMENT
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30 fractions for ⬎ 3 weeks. Chemotherapy consisted of four cycles of cisplatin-etoposide. The accelerated regimen resulted in improved local control (intrathoracic failure: accelerated therapy arm, 36%; standard therapy arm, 52%) and long-term survival, which was 26% for the twice-daily regimen and 16% for the standard regimen. There was an increased rate of grade 3 esophagitis (26% vs 11%, respectively), but there were no other significant differences in toxicity.40 The North Central Cancer Treatment Group41 also compared twice-daily fractionation to daily fractionation but with a significantly different twice-daily regimen and overall study design. In both arms of the study, radiation therapy was administered concurrently with the fourth and fifth cycles of chemotherapy. The standard radiation regimen was 50.4 Gy in 28 fractions for ⬎ 5 weeks. Patients in the twicedaily arm of the study received 48 Gy in three fractions, with a 2.5-week split after the initial 24-Gy dose. Thus, unlike the above-mentioned North American Intergroup trial, there was no overall acceleration of the radiation course. In this trial, there were no differences in local control or survival between patients in the two arms of the study. Radiation Target Volume SCLC often presents with bulky mediastinal adenopathy and often with a confusing mixture of tumor and atelectasis in lung parenchyma. Radiation target volumes are often large, limiting the achievable doses. In attempting to define the minimal appropriate dose, the following two issues can be considered: 1. Is elective radiation applied to normal-appearing lymph nodes required? This has not been studied prospectively. However, the North American Intergroup trial, which produced the best 5-year survival rate reported by a cooperative group, limited elective radiation with no intentional radiation to the contralateral hilum or to supraclavicular nodes, unless there was bulky superior mediastinal adenopathy.42 2. If TRT is started after several cycles of chemotherapy, can the target volume comprise the postchemotherapy rather than the prechemotherapy tumor volume? A retrospective review41,43,44 of data from the Mayo Clinic and the North Central Cancer Treatment Group suggests that this can be done, as recurrences tended to be at the center of the tumor rather that at the periphery. An earlier trial by the Southwest Oncology Group,45 which randomized patients having partial responses to radia266S
tion to prechemotherapy or postchemotherapy volumes, also reported no difference in recurrence rates. Recommendations 12. Patients with limited-stage SCLC should be referred to a radiation oncologist and a medical oncologist for chemotherapy and radiation therapy. Level of evidence, good; benefit, substantial; grade of recommendation, A 13. Patients with limited-stage SCLC achieving a CR should be offered PCI. Level of evidence, good; benefit, substantial; grade of recommendation, A
PCI Brain metastases are common in SCLC. In patients who achieve a CR to induction therapy, CNS metastases will emerge over the next 2 years in about 50 to 60% of patients, and 20 to 30% of these metastases will be the sole site of disease recurrence.46 Overt metastatic disease in the brain, while often responding temporarily to radiation or chemotherapy, is rarely if ever cured. The hypothesis that moderate doses of radiation given to patients without detectable CNS involvement might eradicate occult metastatic disease has been entertained for ⬎ 20 years,47 but only in the past few years have data emerged to allow a reasonable consensus that PCI can reduce the risk of CNS failure and improve survival, and can do so without excessive toxicity.48 –50 A meta-analysis of randomized trials of PCI in complete responders (patients predominately with limited disease) concluded that it significantly reduced CNS failure by about 50% and produced a modest (about 5%) but also significant improvement in the 3-year survival rate. There was a trend toward better results with higher doses (ie, 30 to 36 Gy using 2-Gy fractions) than with 20-Gy doses, but this was not a randomized comparison. An intergroup trial is currently comparing 25-Gy doses administered in 10 fractions to 36-Gy doses administered in 18 fractions. Earlier trials of PCI had variably reported late neurotoxicity, with deterioration in memory, calculation ability, and quality of life. The relation of these toxicities to treatment was unclear. In several more recent trials51 in which cognitive function was assessed prospectively, significant differences between SCLC patients and age-matched and gendermatched control subjects have been observed prior to any treatment, with up to 40% of patients showing significant impairment. Significant further deterioration following PCI was not seen in a large 1997 trial Lung Cancer Guidelines
in the United Kingdom.52 Van Oosterhout et al53 performed careful neurologic and neurophysiologic examinations of 59 survivors who were alive ⬎ 2 years after receiving a diagnosis and who underwent a cranial CT or MRI scan. Groups were neurophysiologically compared with matched control subjects. The authors concluded that although more intensively systemically treated patients showed more neurologic impairment, there was no statistical evidence for additional neurotoxicity with PCI.
therapy to the chest and brain. There was no difference in survival between the arms of the study. For all patients, the median survival time was 15 months and the 2-year survival rate was 20%. All patients who are being worked up for surgery should have undergo mediastinoscopy prior to undergoing resection. The utility of mediastinoscopy in SCLC patients has been validated recently in a small prospective Japanese trial.68 Recommendations
Recommendations 14. Patients with limited-stage SCLC achieving a CR or patients who have undergone resection who have stage I disease should be offered PCI. Level of evidence, good; benefit, substantial; grade of recommendation, A 15. Patients with extensive-stage SCLC achieving a CR should be offered PCI. Level of evidence, fair; benefit, small; grade of recommendation, C
16. For the rare patient with very limited-stage disease (ie, T1–2, N0 tumors), surgical resection followed by a platinum-based chemotherapy could be offered. Level of evidence, fair; benefit, small; grade of recommendation, C 17. Mediastinoscopy should be performed in all patients undergoing surgical resection. Level of evidence, poor; benefit, moderate; grade of recommendation, C 18. PCI should be offered to patients achieving a CR. Level of evidence, fair; benefit, small; grade of recommendation, C
Role of Surgery in Early Stage SCLC The role of surgery in the treatment of earlystage SCLC recently has been reviewed.54 Surgery as a primary modality of treatment was abandoned after the British Medical Counsel55 published the results of their study comparing primary radiation therapy with surgery in patients with resectable SCLC with a 10-year follow-up. The overall survival was better for patients in the radiation therapy-alone arm of the study, and there were no long-term survivors among patients in the surgery arm of the study. However, subsequent reports published in the 1970s and early 1980s showed long-term survival in patients who had been treated with surgery alone who had very earlystage disease. The most favorable subset of patients had T1N0 tumors that had been identified either at the time of surgery or at the time of postoperative pathologic examination.56 –59 Even though the role of adjuvant therapy has not been evaluated in prospective randomized trials, there are several reports58,60 – 66 suggesting a benefit for adjuvant chemotherapy even in the earliest stages of the disease. The role of surgery in node-positive patients was evaluated prospectively by the Lung Cancer Study Group.67 Patients with stage I disease (ie, T1–2,N0 tumors) were excluded from this trial. Patients were initially treated with five cycles of CAV. Responding patients were randomized to undergo surgery or not to undergo surgery. All patients received radiation www.chestjournal.org
Conclusion The incidence of SCLC has been decreasing, and in 1998 it was reported to be 13.8% of all lung cancers. A two-stage staging system is generally utilized. Limited-stage SCLC is optimally treated with a concurrent chemotherapy and radiation therapy approach, and approximately 20% of patients are cured. A platinum-based chemotherapy is the standard for treating extensive-stage SCLC. PCI provides a small absolute benefit in survival in patients achieving CRs. Future research should be focused on optimizing chemotherapy regimens and radiation therapy schedules.
Summary of Recommendations Staging of SCLC 1. In all patients, routine staging of SCLC should include history and physical examinations, complete blood counts, a comprehensive chemistry panel, a CT scan of the chest and abdomen, a CT or MRI scan of the brain, and a bone scan. Level of evidence, good; benefit, substantial; grade of recommendation, A 2. For the routine staging of patients with SCLC, PET scanning is not recommended outside of a clinical trial. Level of evidence, fair; benefit, none/negative; grade of recommendation, D CHEST / 123 / 1 / JANUARY, 2003 SUPPLEMENT
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Treatment of Extensive-Stage SCLC First-Line Treatment: 3. Patients with extensive stage disease should receive platinum-based chemotherapy. Level of evidence, good; benefit, substantial; grade of recommendation, A 4. Patients achieving CRs should be offered PCI. Level of evidence, fair; benefit, small; grade of recommendation, C Maintenance Treatment: 5. For patients with extensive-stage or limitedstage SCLC achieving a partial response or a CR, there is no evidence, outside of a clinical trial, for the use of maintenance treatment. Level of evidence, good; benefit, none/negative; grade of recommendation, D Treatment of Relapsed or Refractory SCLC 6. Patients with SCLC who have relapsed following an initial response to treatment or who are refractory to the initial treatment should be offered further chemotherapy. The chemotherapy offered will depend on the duration of the response after receiving first-line chemotherapy or the lack of response to first-line chemotherapy (ie, sensitive relapses vs refractory patients). Level of evidence, fair; benefit, small/weak; grade of recommendation, C Treatment of Elderly (⬎ 70 years of age) Patients With Extensive-Stage SCLC 7. Elderly patients with good performance status and with intact organ function should be treated with platinum-based chemotherapy. Level of evidence, good; benefit, moderate; grade of recommendation, B 8. Elderly patients with poor prognostic factors such as poor performance status or severe concomitant comorbid disease may still be considered for chemotherapy. Level of evidence, poor; benefit, small; grade of recommendation, C 9. Elderly patients achieving CRs should be offered PCI. Level of evidence, fair; benefit, small; grade of recommendation, C Dose Intensity in SCLC 10. For patients with either extensive-stage or limited-stage SCLC, there is no role for the administration of dose-dense/intense, initial/induction, or maintenance treatment outside of a clinical trial. Level of evidence, good; benefit, none/ negative; grade of recommendation, D 268S
The Role of Growth Factor and the Use of Stem Cell Support in SCLC 11. In patients with SCLC who are receiving chemotherapy, the routine use of growth factor is not recommended. Level of evidence, good; benefit, none/negative; grade of recommendation, D Treatment of Limited-Stage SCLC 12. Patients with limited-stage SCLC should be referred to a radiation oncologist and a medical oncologist for chemotherapy and radiation therapy. Level of evidence, good; benefit, substantial; grade of recommendation, A 13. Patients with limited-stage SCLC achieving CRs should be offered PCI. Level of evidence, good; benefit, substantial; grade of recommendation, A PCI 14. Patients with limited-stage SCLC achieving CRs or patients who have undergone resection who have stage I disease should be offered PCI. Level of evidence, good; benefit, substantial; grade of recommendation, A 15. Patients with extensive-stage SCLC achieving CRs should be offered PCI. Level of evidence, fair; benefit, small; grade of recommendation, C Role of Surgery in Early-Stage SCLC 16. For the rare patient with very limited-stage disease (ie, T1–2,N0 tumors), surgical resection followed by platinum-based chemotherapy could be offered. Level of evidence, fair; benefit, small; grade of recommendation, C 17. Mediastinoscopy should be performed in all patients undergoing surgical resection. Level of evidence, poor; benefit, moderate; grade of recommendation, C 18. PCI should be offered to patients achieving CRs. Level of evidence, fair; benefit, small; grade of recommendation, C
References 1 Page NC, Read WL, Tierney RM, et al. The epidemiology of small cell lung cancer [abstract]. Proc Am Soc Clin Oncol 2002; 21:305a 2 Hauber HP, Bohuslavizki KH, Lund CH, et al. Positron emission tomography in the staging of small-cell lung cancer: a preliminary study. Chest 2001; 119:950 –954 3 Schumacher T, Brink I, Mix M, et al. FDG-PET imaging for Lung Cancer Guidelines
4
5
6 7 8 9
10
11
12 13
14
15
16 17
18
19 20
the staging and follow-up of small cell lung cancer. Eur J Nucl Med 2001; 28:483– 488 Pujol JL, Carestia L, Daures JP. Is there a case for cisplatin in the treatment of small-cell lung cancer?: a meta-analysis of randomized trials of a cisplatin-containing regimen vs a regimen without this alkylating agent. Br J Cancer 2000; 83:8 –15 Berghmans T, Paesmans M, Mascaux C, et al. A metaanalysis of the role of etoposide (VP-16) and cisplatin (CDDP) in small cell lung cancer (SCLC) with a methodology assessment [abstract]. Eur J Cancer 1999; 35(suppl): s248 Chute JP, Chen T, Feigal E, et al. Twenty years of phase III trials for patients with extensive-stage small-cell lung cancer: perceptible progress. J Clin Oncol 1999; 17:1794 –1801 Brahmer JR, Ettinger DS. Carboplatin in the treatment of lung cancer. Oncologist 1998; 3:143–154 Noda K, Nishiwaki Y, Kawahara M, et al. Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small cell lung cancer. N Engl J Med 2002; 346:85–91 Loehrer PJ Sr, Ansari R, Gonin R, et al. Cisplatin plus etoposide with and without ifosfamide in extensive small-cell lung cancer: a Hoosier Oncology Group study. J Clin Oncol 1995; 13:2594 –2599 Mavroudis D, Papadakis E, Veslemes M, et al. A multicenter randomized clinical trial comparing paclitaxel-cisplatinetoposide vs cisplatin-etoposide as first-line treatment in patients with small-cell lung cancer. Ann Oncol 2001; 12:463– 470 Niell HB, Herndon JE, Miller AA, et al. Randomized phase III intergroup trial (CALGB 9732) of etoposide (VP-16) and cisplatin (DDP) with or without paclitaxel (TAX) and G-CSF in patients with extensive stage small cell lung cancer (EDSCLC) [abstract]. Proc Am Soc Clin Oncol 2002; 21:293a Sculier JP, Berghmans T, Castaigne C, et al. Maintenance chemotherapy for small cell lung cancer: a critical review of the literature. Lung Cancer 1998; 19:141–151 Schiller JH, Adak S, Cella D, et al. Topotecan vs observation after cisplatin plus etoposide in extensive-stage small-cell lung cancer: E7593; a phase III trial of the Eastern Cooperative Oncology Group. J Clin Oncol 2001; 19:2114 –2122 Yuen AR, Zou G, Turrisi AT, et al. Similar outcome of elderly patients in intergroup trial 0096: cisplatin, etoposide, and thoracic radiotherapy administered once or twice daily in limited stage small cell lung carcinoma. Cancer 2000; 89:1953–1960 Quon H, Shepherd FA, Payne DG, et al. The influence of age on the delivery, tolerance, and efficacy of thoracic irradiation in the combined modality treatment of limited stage small cell lung cancer. Int J Radiat Oncol Biol Phys 1999; 43:39 – 45 Ando M, Minami H, Ando Y, et al. Pharmacological analysis of etoposide in elderly patients with lung cancer. Clin Cancer Res 1999; 5:1690 –1695 Girling DJ. Comparison of oral etoposide and standard intravenous multidrug chemotherapy for small-cell lung cancer: a stopped multicentre randomised trial; Medical Research Council Lung Cancer Working Party. Lancet 1996; 348:563–566 Souhami RL, Spiro SG, Rudd RM, et al. Five-day oral etoposide treatment for advanced small-cell lung cancer: randomized comparison with intravenous chemotherapy. J Natl Cancer Inst 1997; 89:577–580 Matsui K, Masuda N, Fukuoka M, et al. Phase II trial of carboplatin plus oral etoposide for elderly patients with small-cell lung cancer. Br J Cancer 1998; 77:1961–1965 Murray N, Grafton C, Shah A, et al. Abbreviated treatment
www.chestjournal.org
21
22
23
24
25
26 27 28
29
30
31
32
33 34
for elderly, infirm, or noncompliant patients with limitedstage small-cell lung cancer. J Clin Oncol 1998; 16:3323– 3328 Westeel V, Murray N, Gelmon K, et al. New combination of the old drugs for elderly patients with small-cell lung cancer: a phase II study of the PAVE regimen. J Clin Oncol 1998; 16:1940 –1947 Steele JP. Gemcitabine/carboplatin vs cisplatin/etoposide for patients with poor-prognosis small cell lung cancer: a phase III randomized trial with quality-of-life evaluation. Semin Oncol 2001; 28(suppl):15–18 White SC, Lorigan P, Middleton MR, et al. Randomized phase II study of cyclophosphamide, doxorubicin, and vincristine compared with single-agent carboplatin in patients with poor prognosis small cell lung carcinoma. Cancer 2001; 92:601– 608 Sculier JP, Paesmans M, Bureau G, et al. Multiple-drug weekly chemotherapy vs standard combination regimen in small-cell lung cancer: a phase III randomized study conducted by the European Lung Cancer Working Party. J Clin Oncol 1993; 11:1858 –1865 Souhami RL, Rudd R, Ruiz de Elvira MC, et al. Randomized trial comparing weekly vs 3-week chemotherapy in small- cell lung cancer: a Cancer Research Campaign trial. J Clin Oncol 1994; 12:1806 –1813 Fukuoka M, Masuda N, Negoro S, et al. CODE chemotherapy with and without granulocyte colony-stimulating factor in small-cell lung cancer. Br J Cancer 1997; 75:306 –309 Murray N, Shah A, Osoba D, et al. Intensive weekly chemotherapy for the treatment of extensive-stage small-cell lung cancer. J Clin Oncol 1991; 9:1632–1638 Furuse K, Fukuoka M, Nishiwaki Y, et al. Phase III study of intensive weekly chemotherapy with recombinant human granulocyte colony-stimulating factor vs standard chemotherapy in extensive-disease small-cell lung cancer: the Japan Clinical Oncology Group. J Clin Oncol 1998; 16: 2126 –2132 Skarlos DV, Samantas E, Pectasides D, et al. Weekly alternating non-cross-resistant chemotherapy for small cell lung cancer with a good prognosis: a study of the Hellenic Cooperative Oncology Group. Am J Clin Oncol 1999; 22:87–93 Pujol JL, Douillard JY, Riviere A, et al. Dose-intensity of a four-drug chemotherapy regimen with or without recombinant human granulocyte-macrophage colony-stimulating factor in extensive-stage small-cell lung cancer: a multicenter randomized phase III study. J Clin Oncol 1997; 15:2082–2089 Steward WP, von Pawel J, Gatzemeier U, et al. Effects of granulocyte-macrophage colony-stimulating factor and dose intensification of V-ICE chemotherapy in small-cell lung cancer: a prospective randomized study of 300 patients. J Clin Oncol 1998; 16:642– 650 Thatcher N, Girling DJ, Hopwood P, et al. Improving survival without reducing quality of life in small-cell lung cancer patients by increasing the dose-intensity of chemotherapy with granulocyte colony-stimulating factor support: results of a British Medical Research Council Multicenter Randomized Trial; Medical Research Council Lung Cancer Working Party. J Clin Oncol 2000; 18:395– 404 Arriagada R, Le Chevalier T, Pignon JP, et al. Initial chemotherapeutic doses and survival in patients with limited small-cell lung cancer. N Engl J Med 1993; 329:1848 –1852 Chouaid C, Bassinet L, Fuhrman C, et al. Routine use of granulocyte colony-stimulating factor is not cost-effective and does not increase patient comfort in the treatment of small-cell lung cancer: an analysis using a Markov model. J Clin Oncol 1998; 16:2700 –2707 CHEST / 123 / 1 / JANUARY, 2003 SUPPLEMENT
269S
35 Warde P, Payne D. Does thoracic irradiation improve survival and local control in limited-stage small-cell carcinoma of the lung? A meta-analysis. J Clin Oncol 1992; 10:890– 895 36 Pignon JP, Arriagada R, Ihde DC, et al. A meta-analysis of thoracic radiotherapy for small-cell lung cancer. N Engl J Med 1992; 327:1618 –1624 37 Murray N, Coldman A. The relationship between the thoracic irradiation timing and long-term survival in combined modality therapy of limited stage small cell lung cancer(LSCLC) [abstract]. Proc Am Soc Clin Oncol 1995; 14 38 Choi NC, Carey RW. Importance of radiation dose in achieving improved loco-regional tumor control in limited stage small-cell lung carcinoma: an update. Int J Radiat Oncol Biol Phys 1989; 17:307–310 39 Choi NC, Herndon JE 2nd, Rosenman J, et al. Phase I study to determine the maximum-tolerated dose of radiation in standard daily and hyperfractionated-accelerated twice-daily radiation schedules with concurrent chemotherapy for limitedstage small-cell lung cancer. J Clin Oncol 1998; 16:3528–3536 40 Turrisi AT 3rd, Kim K, Blum R, et al. Twice-daily compared with once-daily thoracic radiotherapy in limited small-cell lung cancer treated concurrently with cisplatin and etoposide. N Engl J Med 1999; 340:265–271 41 Maksymiuk AW, Jett JR, Earle JD, et al. Sequencing and schedule effects of cisplatin plus etoposide in small-cell lung cancer: results of a North Central Cancer Treatment Group randomized clinical trial. J Clin Oncol 1994; 12:70 –76 42 Turrisi AT 3rd, Glover DJ, Mason BA. A preliminary report: concurrent twice-daily radiotherapy plus platinum- etoposide chemotherapy for limited small cell lung cancer. Int J Radiat Oncol Biol Phys 1988; 15:183–187 43 Bonner JA, Sloan JA, Shanahan TG, et al. Phase III comparison of twice-daily split-course irradiation vs oncedaily irradiation for patients with limited stage small-cell lung carcinoma. J Clin Oncol 1999; 17:2681–2691 44 Liengswangwong V, Bonner JA, Shaw EG, et al. Limitedstage small-cell lung cancer: patterns of intrathoracic recurrence and the implications for thoracic radiotherapy. J Clin Oncol 1994; 12:496 –502 45 Kies MS, Mira JG, Crowley JJ, et al. Multimodal therapy for limited small-cell lung cancer: a randomized study of induction combination chemotherapy with or without thoracic radiation in complete responders; and with wide-field vs reduced- field radiation in partial responders—a Southwest Oncology Group Study. J Clin Oncol 1987; 5:592– 600 46 Arriagada R, Le Chevalier T, BF, et al. Randomized trial of on prophylactic cranial irradiation (PCI) for patients with small cell lung cancer (SCLC) in complete remission [abstract]. Proc Am Soc Clin Oncol 1994; 13 47 Hansen HH, Dombernowsky P, Hirsch FR, et al. Prophylactic irradiation in bronchogenic small cell anaplastic carcinoma: a comparative trial of localized vs extensive radiotherapy including prophylactic brain irradiation in patients receiving combination chemotherapy. Cancer 1980; 46:279–284 48 Auperin A, Arriagada R, Pignon JP, et al. Prophylactic cranial irradiation for patients with small-cell lung cancer in complete remission: Prophylactic Cranial Irradiation Overview Collaborative Group. N Engl J Med 1999; 341:476– 484 49 Kotalik J, Yu E, Markman BR, et al. Practice guideline on prophylactic cranial irradiation in small-cell lung cancer. Int J Radiat Oncol Biol Phys 2001; 50:309 –316 50 PCIOC G. Cranial Irradiation for preventing brain metastases of small cell lung cancer in complete remission. Cochrane Database Syst Rev 2000; 4:CD002805 51 Cull A, Gregor A, Hopwood P, et al. Neurological and cognitive impairment in long-term survivors of small cell lung cancer. Eur J Cancer 1994; 8:1067–1074 270S
52 Gregor A, Cull A, Stephens RJ, et al. Prophylactic cranial irradiation is indicated following complete response to induction therapy in small cell lung cancer: results of a multicentre randomised trial; United Kingdom Coordinating Committee for Cancer Research (UKCCCR) and the European Organization for Research and Treatment of Cancer (EORTC). Eur J Cancer 1997; 33:1752–1758 53 Van Oosterhout AG, Ganzevles PG, Wilmink JT, et al. Sequelae in long-term survivors of small cell lung cancer. Int J Radiat Oncol Biol Phys 1996; 34:1037–1044 54 Simon GR, Ginsberg RJ, Ruckdeschel J. Small-cell lung cancer. Chest Surg Clin N Am 2001; 11:165–188 55 Fox W, Scadding JG. Medical Research Council comparative trial of surgery and radiotherapy for primary treatment of small-celled or oat-celled carcinoma of bronchus: ten-year follow-up. Lancet 1973; 2:63– 65 56 Higgins GA, Shields TW, Keehn RJ. The solitary pulmonary nodule: ten-year follow-up of veterans administration-armed forces cooperative study. Arch Surg 1975; 110:570 –575 57 Lennox SC, Flavell G, Pollock DJ, et al. Results of resection for oat-cell carcinoma of the lung. Lancet 1968; 2:925–927 58 Miyazawa N, Tsuchiya R, Naruke T, et al. A clinicopathological study of surgical treatment for small cell carcinoma of the lung. Jpn J Clin Oncol 1986; 16:297–307 59 Shields TW, Higgins GA Jr, Matthews MJ, et al. Surgical resection in the management of small cell carcinoma of the lung. Thorac Cardiovasc Surg 1982; 84:481– 488 60 Lucchi M, Mussi A, Chella A, et al. Surgery in the management of small cell lung cancer. Eur J Cardiothorac Surg 1997; 12:689 – 693 61 Merkle NM, Mickisch GH, Kayser K, et al. Surgical resection and adjuvant chemotherapy for small cell carcinoma. Thorac Cardiovasc Surg 1986; 34:39 – 42 62 Maassen W, Greschuchna D. Small cell carcinoma of the lung: to operate or not?; surgical experience and results. Thorac Cardiovasc Surg 1986; 34:71–76 63 Karrer K, Shields TW, Denck H, et al. The importance of surgical and multimodality treatment for small cell bronchial carcinoma. Thorac Cardiovasc Surg 1989; 97:168 –176 64 Osterlind K, Hansen M, Hansen HH, et al. Influence of surgical resection prior to chemotherapy on the long-term results in small cell lung cancer: a study of 150 operable patients. Eur J Cancer Clin Oncol 1986; 22:589 –593 65 Shepherd FA, Ginsberg RJ, Feld R, et al. Surgical treatment for limited small-cell lung cancer: the University of Toronto Lung Oncology Group experience. Thorac Cardiovasc Surg 1991; 101:385–393 66 Friess GG, McCracken JD, Troxell ML, et al. Effect of initial resection of small-cell carcinoma of the lung: a review of Southwest Oncology Group Study 7628. J Clin Oncol 1985; 3:964 –968 67 Lad T, Piantadosi S, Thomas P, et al. A prospective randomized trial to determine the benefit of surgical resection of residual disease following response of small cell lung cancer to combination chemotherapy. Chest 1994; 106(suppl): 320S–323S 68 Inoue M, Nakagawa K, Fujiwara K, et al. Results of preoperative mediastinoscopy for small cell lung cancer. Ann Thorac Surg 2000; 70:1620 –1623 69 Nakanishi Y, Kawarada Y, Hirose N, et al. Phase II trial of combination chemotherapy with cisplatin, carboplatin and etoposide in stage IIIB and IV small-cell lung cancer: Fukuoka Lung Cancer Study Group. Cancer Chemother Pharmacol 1998; 41:453– 456 70 Glisson BS, Kurie JM, Perez-Soler R, et al. Cisplatin, etoposide, and paclitaxel in the treatment of patients with Lung Cancer Guidelines
71
72
73 74
75
76 77
78 79
80 81
82
83 84
85 86 87
extensive small-cell lung carcinoma. J Clin Oncol 1999; 17:2309 –2315 Kelly K, Crowley J, Bunn PA, et al. A randomized phase III trial of paclitaxel plus carboplatin (PC) versus vinorelbine plus cisplatin (VC) in untreated advanced non-small cell lung cancer (NSCLC): a South West Oncology Group (SWOG) Trial [abstract]. Proc Am Soc Clin Oncol 1999; 18:461a Kudoh S, Fujiwara Y, Takada Y, et al. Phase II study of irinotecan combined with cisplatin in patients with previously untreated small-cell lung cancer. J Clin Oncol 1998; 16:1068 –1074 Hickish TF SE, Nicolson MC, et al. A pilot study of MVP (mitomycin-C, vinblastine and cisplatin) chemotherapy in small-cell lung cancer. Br J Cancer 1998; 77:1966 –1970 Kalemkerian GP, Jiroutek M, Ettigner DS, et al. A phase II study of all-trans-retinoic acid plus cisplatin and etoposide in patients with extensive stage lung carcinoma. Cancer 1998; 83:1102–1108 Lyss AP, Herndon JE, Lynch TC, et al. Paclitaxel ⫹ cisplatin ⫹ G-CSF in patients with previously untreated extensive stage small cell lung cancer (E-SCLC): preliminary analysis of Cancer and Leukemia Group B (CALBG) 9430 [abstract]. Proc Am Soc Clin Oncol 1999; 18:468a Jacobs SA, Jett JR, Belani CP, et al. Topotecan and paclitaxel, and active couplet, in untreated extensive disease small cell lung cancer [abstract]. Proc Am Soc Clin Oncol 1999; 18:470a Nakamura S, Kudoh S, Komuta K, et al Phase II. study of irinotecan (CPT-11) combined with etoposide (VP-16) for previously untreated extensive-disease small-cell lung cancer (ED-SCLC) [abstract]. Proc Am Soc Clin Oncol 1999; 18:470S Deppermanan KM, Serke M, Oehm C, et al. Paclitaxel (TAX), and carboplatin (CBDA) in advaned SCLC: a phase II study [abstract]. Proc Am Soc Clin Oncol 1999; 48:482a Rushing DA, Tipping SJ, Clouse LH, et al. Phase 1 study of the combination of irinotecan (CPT-11) and paclitaxel (Taxol) in previously treated patients with small cell carcinoma of the lung (SCCL) [abstract]. Proc Am Soc Clin Oncol 1999; 18:484a Lad T, Mauer A, Hoffman P, et al. Phase II trial of paclitaxel and doxorubicin in small cell lung cancer [abstract]. Proc Am Soc Clin Oncol 1999; 18:513a Lianes P, Moreno JA, Sevilla I, et al. Phase II study of docetaxel and cisplatin in first line treatment of disseminated small cell lung cancer (E-SCLC) [abstract]. Proc Am Soc Clin Oncol 1999; 18:541a Lynch TJ, Herndon JE, Lilenbaum RD, et al. Toxicity of paclitaxel (P) and topotecan (T) in patients with previously untreated extensive small cell lung cancer [abstract]. Proc Am Soc Clin Oncol 1999; 18:515a Tweedy CR, Andrews DR, Ball T. Topotecan and paclitaxel in extensive stage small cell lung cancer as initial therapy [abstract]. Proc Am Soc Clin Oncol 1999; 18:525a Panza N, Frasci G, Comella P, et al. Cisplatin-paclitaxeltopotecan (CPT) weekly administration in chemonaive or pretreated extensive disease small cell lung cancer (EDSCLC). Eur J Cancer 1999; 35:S253 Baldini E, Chella A, del Freo A, et al. Paclitaxel/epirubicin/ etoposide in patients with extensive-disease small-cell lung cancer (SCLC) [abstract]. Eur J Cancer 1999; 35:S257 Masuda N, Matsui K, Negoro S, et al. Combination of irinotecan and etoposide for treatment of refractory or relapsed small-cell lung cancer. J Clin Oncol 1998; 16:3329–3334 Ardizzoni A, Manegold G, Gaffaar R, et al. Combination chemotherapy with cisplatin and topotecan as second-line treatment of sensitive and refractory small cell lung cancer(SCLC): an EORTC LCCG phase II study [abstract]. Proc Am Soc Clin Oncol 1999; 18:478a
www.chestjournal.org
88 Lusch G, Rausch G, and Kosierowski R. Phase II study of daily oral etoposide and hexamethylmelamine (altretamine) in relapsed small cell lung cancer (SCLC) [abstract]. Proc Am Soc Clin Oncol 1999; 18:478a 89 Rushing DA, Tipping SJ, Close LH, et al. Phase I study of combination of irinotecan (CPT-11) and paclitaxel (Taxol) in previously treated patients with small cell lung cancer (SCLC) [abstract]. Proc Am Soc Clin Oncol 1999; 18:484a 90 Agelaki S, Agelidou A, Blazogiannakis G, et al. A phase II study of paclitaxel (P) and carboplatin (C) as second-line treatment in patients with small cell lung cancer. Eur J Cancer 1999; 35:S258 91 Perry MC, Herndon JE 3rd, Eaton WL, et al. Thoracic radiation therapy added to chemotherapy for small-cell lung cancer: an update of Cancer and Leukemia Group B Study 8083. J Clin Oncol 1998; 16:2466 –2467 92 Murray N, Coy P, Pater JL, et al. Importance of timing for thoracic irradiation in the combined modality treatment of limited-stage small-cell lung cancer: the National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol 1993; 11(2):336 –344 93 Shultz HP, Nielsen OS, Sell A, et al. Timing of chest irradiation with respect to combination chemotherapy in small cell lung cancer, limited disease. [abstract]. Lung Cancer 1988; 4:153 94 Tsukada H, Yokoyama A, Goto K, et al. Concurrent vs sequential radiotherapy for small cell lung cancer. Semin Oncol 2001; 28(suppl):23–26 95 Gregor A, Drings P, Burghouts J, et al. Randomized trial of alternating vs sequential radiotherapy/chemotherapy in limiteddisease patients with small-cell lung cancer: a European Organization for Research and Treatment of Cancer Lung Cancer Cooperative Group Study. J Clin Oncol 1997; 15:2840–2849 96 LeBeau B, Chastang C, Urban T, et al. A randomized clinical trial comparing concurrent and alternated thoracic irradiation in limited stage small cell lung cancer [abstract]. Proc Am Soc Clin Oncol 1996; 15:383 97 Work E, Nielsen OS, Bentzen SM, et al. Randomized study of initial vs late chest irradiation combined with chemotherapy in limited-stage small-cell lung cancer: Aarhus Lung Cancer Group. J Clin Oncol 1997; 15:3030 –3037 98 Samantas E, Fountzilas G, Briasoulis T, et al. Randomized comparison of early vs late twice-daily chest irradiation therapy concurrently with chemotherapy in limited disease small cell lung cancer: final results [abstract]. Proc Am Soc Clin Oncol 2000; 491A 99 Jeremic B, Shibamoto Y, Acimovic L et al. Initial vs delayed accelerated hyperfractionated radiation therapy and concurrent chemotherapy in limited small-cell lung cancer: a randomized study. J Clin Oncol 1997; 15:893–900 100 Wagner H Jr. Radiation therapy in the management of limited small cell lung cancer: when, where, and how much? Chest 1998; 113(suppl):92S–100S 101 von Pawel J, Schiller JH, Shepherd FA, et al. Topotecan vs cyclophosphamide, doxorubicin, and vincristine for the treatment of recurrent small-cell lung cancer. J Clin Oncol 1999; 17:658 – 667 102 Schirrmeister H, Glatting G, Hetzel J, et al. Prospective evaluation of the clinical value of planar bone scans, SPECT, and (18)F-labeled NaF PET in newly diagnosed lung cancer. J Nucl Med 2001; 42:1800 –1804 103 Kosmidis PA, Samantas E, Fountzilas G, et al. Cisplatin/ etoposide vs carboplatin/etoposide chemotherapy and irradiation in small cell lung cancer: a randomized phase III study. Semin Oncol 1994; 21(suppl):23–30
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