Evans W K, Feld R, Osoba D, Shepherd F A, Dill J, Deboer G
Cancer. 1984 Apr 1;53(7):1461-6. doi: 10.1002/1097-0142(19840401)53:7<1461::aid-cncr2820530706>3.0.co;2-n.
Fifty-four patients with small cell cancer of the lung (SCCL) who failed to respond to induction chemotherapy or relapsed within 3 months of its completion were treated either with VP-16 alone or VP-16 and cisplatin. Fifty-two patients were initially treated with cyclophosphamide, doxorubicin (Adriamycin) and vincristine (CAV), and two were treated with cyclophosphamide, methotrexate, and vincristine. Nine patients also received other drug combinations either as maintenance therapy or as treatment for relapse. Fourteen of 18 patients treated with VP-16 alone were evaluable for response, and there was only one partial remission. On the other hand, 15 of the 34 evaluable patients (44%) treated with VP-16 and cisplatin had a partial response, and an additional 11 patients (32%) showed substantial tumor regression and were classified as improved. Two patients had stable disease, and six (18%) progressed. Five of the nine (55.6%) limited-disease patients achieved a partial response compared with 10 of 25 (40%) with extensive disease. The median survival time from the date of first treatment with the combination was 17 weeks (29 weeks for patients achieving a partial response; 19 weeks for those showing improvement; 11 weeks for those with stable disease; and 13 weeks for patients with disease progression). Gastrointestinal toxicity was mild relative to that of CAV-induction therapy but myelosuppression, particularly thrombocytopenia, was common. Mild nephrotoxicity occurred in four patients, but no other important toxicities were identified.
54例小细胞肺癌(SCCL)患者,对诱导化疗无反应或在化疗完成后3个月内复发,接受了单独使用依托泊苷或依托泊苷与顺铂联合的治疗。52例患者最初接受了环磷酰胺、阿霉素(阿霉素)和长春新碱(CAV)治疗,2例患者接受了环磷酰胺、甲氨蝶呤和长春新碱治疗。9例患者还接受了其他药物联合治疗,作为维持治疗或复发治疗。18例单独接受依托泊苷治疗的患者中有14例可评估反应,仅1例部分缓解。另一方面,34例可评估的接受依托泊苷和顺铂联合治疗的患者中有15例(44%)部分缓解,另外11例患者(32%)肿瘤显著消退,被归类为病情改善。2例患者病情稳定,6例(18%)病情进展。9例局限性疾病患者中有5例(55.6%)部分缓解,而25例广泛性疾病患者中有10例(40%)部分缓解。从首次接受联合治疗之日起的中位生存时间为17周(部分缓解患者为29周;病情改善患者为19周;病情稳定患者为11周;病情进展患者为13周)。与CAV诱导治疗相比,胃肠道毒性较轻,但骨髓抑制,尤其是血小板减少症较为常见。4例患者出现轻度肾毒性,但未发现其他重要毒性。