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广泛期小细胞肺癌长期生存率的提高。

Improvement of long-term survival in extensive small-cell lung cancer.

作者信息

Jackson D V, Case L D, Zekan P J, Powell B L, Caldwell R D, Bearden J D, Nelson E C, Muss H B, Cooper M R, Richards F

机构信息

Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, NC 27103.

出版信息

J Clin Oncol. 1988 Jul;6(7):1161-9. doi: 10.1200/JCO.1988.6.7.1161.

Abstract

The effect of adding the epipodophyllotoxin etoposide (VP-16-213) to a standard chemotherapy regimen for patients with extensive stage small-cell lung cancer was evaluated during a randomized trial. Chemotherapy consisted of vincristine, doxorubicin, and cyclophosphamide (VAC) alone or with etoposide (EVAC). Of 139 patients enrolled, 136 patients were eligible for study and all but five were evaluable for response. The overall objective response was 46% in the VAC group v 70% in the etoposide-treated group (P = .008) with complete response (CR) rates of 12% v 29%, respectively (P = .030). Although the time to the observation of disease progression was significantly longer in the group of patients receiving etoposide (9.6 v 6.5 months, P = .010), overall survival was similar; this was probably due to administration of other agents including etoposide at the time of VAC failure. However, there were noteworthy differences in long-term (greater than or equal to 2 year) survival. Whereas only four (6%) patients treated with VAC lived 2 years, 11 (16%) of the etoposide-treated group did so (P = .100). Two-year failure-free survival was attained in one (2%) of the VAC patients and eight (11%) of the patients treated with etoposide (P = .034). Long-term survivorship, heretofore usually reported in patients with limited stage disease after a variety of treatments, may be possible with this drug combination in the setting of extensive disease.

摘要

在一项随机试验中,评估了在广泛期小细胞肺癌患者的标准化化疗方案中添加表鬼臼毒素依托泊苷(VP - 16 - 213)的效果。化疗方案包括单独使用长春新碱、阿霉素和环磷酰胺(VAC)或联合依托泊苷(EVAC)。在入组的139例患者中,136例符合研究条件,除5例患者外,其余均可评估疗效。VAC组的总体客观缓解率为46%,而依托泊苷治疗组为70%(P = .008),完全缓解(CR)率分别为12%和29%(P = .030)。尽管接受依托泊苷治疗的患者观察到疾病进展的时间明显更长(9.6个月对6.5个月,P = .010),但总生存期相似;这可能是由于在VAC方案失败时给予了包括依托泊苷在内的其他药物。然而,长期(大于或等于2年)生存率存在显著差异。接受VAC治疗的患者中只有4例(6%)存活2年,而依托泊苷治疗组有11例(16%)存活(P = .100)。VAC方案治疗的患者中有1例(2%)实现了2年无失败生存期,依托泊苷治疗的患者中有8例(11%)实现了2年无失败生存期(P = .034)。这种药物组合在广泛期疾病的情况下,可能使长期生存成为可能,而长期生存此前通常在经过各种治疗的局限期疾病患者中报道。

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