Hayashi Y, Kato M, Matsuura T, Yamada Y, Adachi S, Ito G, Yamamoto K, Takeuchi T
First Dept. of Internal Medicine, Nagoya City University, School of Medicine.
Gan To Kagaku Ryoho. 1990 Aug;17(8 Pt 1):1455-60.
Thirty-five patients with non-small cell lung cancer (adenocarcinoma: 15, squamous cell: 15, large cell: 5, Stage I: 3, II: 1, IIIA: 8, IIIB: 5, IV: 18) were treated with combination chemotherapy, CDDP 80 mg/m2 day 1, VDS 3 mg/m2 days 1 & 8, and MMC 8 mg/m2 day 1. This regimen was repeated two times at intervals of four weeks. Sixteen partial responses were observed (response rate of 45.7%), and the median duration of survival for responders was 12.6 +/- 7.5 months and for nonresponders 10.1 +/- 4.8 months. Statistically there was no difference between them, but a survival from the onset of therapy of responders was significantly better (p less than 0.05) than that of non-responders. Toxicity was tolerable with myelosuppression, chemotherapy-induced nausea and vomiting.
35例非小细胞肺癌患者(腺癌15例、鳞癌15例、大细胞癌5例;Ⅰ期3例、Ⅱ期1例、ⅢA期8例、ⅢB期5例、Ⅳ期18例)接受联合化疗,顺铂80mg/m²第1天,长春地辛3mg/m²第1天和第8天,丝裂霉素8mg/m²第1天。该方案每4周重复2次。观察到16例部分缓解(缓解率45.7%),缓解者的中位生存期为12.6±7.5个月,未缓解者为10.1±4.8个月。统计学上两者无差异,但缓解者从治疗开始的生存期显著优于未缓解者(p<0.05)。毒性反应可耐受,包括骨髓抑制、化疗引起的恶心和呕吐。