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61例小细胞肺癌患者联合放化疗方案的结果

Results of a combined chemo-radiotherapeutic program in 61 patients affected by small cell lung cancer.

作者信息

Tummarello D, Guidi F, Porfiri E, Isidori P, Raspugli M, Cellerino R

机构信息

Cattedra di Oncologia Clinica, Università di Ancona.

出版信息

Tumori. 1988 Apr 30;74(2):207-11. doi: 10.1177/030089168807400215.

Abstract

Sixty-one patients affected by small cell lung cancer (SCLC) entered in the study. Eighteen had limited disease and 43 extensive disease. Treatment consisted of: induction chemotherapy with 3 courses of CAV (cyclophosphamide, adriamycin, vincristine) in limited disease patients or 2 courses of CAV plus 2 courses of DDP-VP16 (cisplatin, etoposide) in extensive disease patients, followed by chest radiotherapy and CNS prophylaxis in responsive patients. Subsequently, responders and stable patients received maintenance chemotherapy by the alternation of cycles of CAV, DDP-VP16 and C'MP (CCNU, methotrexate, procarbazine), which lasted 1 year or until relapse. Four of 17 limited disease patients (23%) obtained a CR and 11 (65%) a PR; their median survival was 11 months (range, 2+-36+). One of the 7 extensive disease patients (3%) achieved a CR and 19 (51%) a PR; their median survival was 6 months (range, 1-22). Median duration of response was 12 months for CR and 5 months for PR. Responders (CR and PR) survived 11.5 months versus 3.5 months for failures (P less than 0.05); 3/61 (5%) showed long-term survival, in the absence of disease. The overall median survival was 7 months (range, 1-36+). The main toxic effects were myelosuppression and vomiting (WHO grade 3). From our results, this program does not offer further substantial gains in patients with SCLC.

摘要

61例小细胞肺癌(SCLC)患者进入本研究。其中18例为局限性疾病,43例为广泛性疾病。治疗方案如下:局限性疾病患者接受3个疗程的CAV(环磷酰胺、阿霉素、长春新碱)诱导化疗,广泛性疾病患者接受2个疗程的CAV加2个疗程的DDP-VP16(顺铂、依托泊苷)诱导化疗,随后对反应性患者进行胸部放疗和中枢神经系统预防。随后,反应者和病情稳定的患者通过交替使用CAV、DDP-VP16和C'MP(洛莫司汀、甲氨蝶呤、丙卡巴肼)周期进行维持化疗,持续1年或直至复发。17例局限性疾病患者中有4例(23%)获得完全缓解(CR),11例(65%)获得部分缓解(PR);其中位生存期为11个月(范围为2 +- 36 +)。7例广泛性疾病患者中有1例(3%)获得CR,19例(51%)获得PR;其中位生存期为6个月(范围为1 - 22)。CR患者的中位缓解持续时间为12个月,PR患者为5个月。反应者(CR和PR)的生存期为11.5个月,而未缓解者为3.5个月(P < 0.05);61例中有3例(5%)在无疾病情况下显示长期生存。总体中位生存期为7个月(范围为1 - 36 +)。主要毒性作用为骨髓抑制和呕吐(WHO 3级)。根据我们的结果,该方案并未给SCLC患者带来进一步的显著获益。

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