Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer
- PMID: 11784874
- DOI: 10.1056/NEJMoa003034
Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer
Abstract
Background: Irinotecan hydrochloride, a topoisomerase I inhibitor, is effective against small-cell lung cancer. In a phase 2 study of irinotecan plus cisplatin in patients with extensive small-cell lung cancer, there was a high response rate and a promising median survival time.
Methods: We conducted a multicenter, randomized, phase 3 study in which we compared irinotecan plus cisplatin with etoposide plus cisplatin in patients with extensive (metastatic) small-cell lung cancer.
Results: The planned size of the study population was 230 patients, but enrollment was terminated early because an interim analysis found a statistically significant difference in survival between the patients assigned to receive irinotecan and cisplatin and those assigned to receive etoposide and cisplatin; as a result, only 154 patients were enrolled. The median survival was 12.8 months in the irinotecan-plus-cisplatin group and 9.4 months in the etoposide-plus-cisplatin group (P=0.002 by the unadjusted log-rank test). At two years, the proportion of patients surviving was 19.5 percent in the irinotecan-plus-cisplatin group and 5.2 percent in the etoposide-plus-cisplatin group. Severe or life-threatening myelosuppression was more frequent in the etoposide-plus-cisplatin group than in the irinotecan-plus-cisplatin group, and severe or life-threatening diarrhea was more frequent in the irinotecan-plus-cisplatin group than in the etoposide-plus-cisplatin group.
Conclusions: Irinotecan plus cisplatin is an effective treatment for metastatic small-cell lung cancer.
Comment in
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Lung cancer--time to move on from chemotherapy.N Engl J Med. 2002 Jan 10;346(2):126-8. doi: 10.1056/NEJM200201103460211. N Engl J Med. 2002. PMID: 11784881 No abstract available.
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Irinotecan in small-cell lung cancer.N Engl J Med. 2002 May 2;346(18):1414-5; author reply 1414-5. doi: 10.1056/NEJM200205023461818. N Engl J Med. 2002. PMID: 11986422 No abstract available.
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