Miller T P, Weick J K, Grozea P N, Carlin D A
Cancer Treat Rep. 1982 Mar;66(3):553-6.
Sixty-three previously untreated patients with metastatic non-small cell lung cancer (40 patients with adenocarcinoma and 23 with large cell undifferentiated carcinoma) were treated with combination chemotherapy consisting of 5-FU (300 mg/m2) given as an iv bolus on Days 1-4 and vindesine (3 mg/m2) and mitomycin (10 mg/m2), both given as an iv bolus on Day 1 of each treatment course (FEMi). FEMi was repeated at 3-week intervals for three treatment courses and thereafter at 6-week intervals until disease progression. Major objective responses were seen in 13 of 63 patients (21%). Minor responses were seen in an additional 12 patients (19%). The median survival for all patients was 23 weeks and for responding patients was 38 weeks. The pretreatment performance status had a significant effect on both the response rate and survival time. Patients having an initial Karnofsky performance score greater than or equal to 70% had a 54% response rate, with a median survival of 42 weeks for responding patients. FEMi was well-tolerated: 18 patients (29%) did not have any side effects and only five (8%) experienced vomiting.
63例既往未接受过治疗的转移性非小细胞肺癌患者(40例腺癌患者和23例大细胞未分化癌患者)接受了联合化疗,化疗方案为氟尿嘧啶(5-氟尿嘧啶,300mg/m²)在第1至4天静脉推注,长春地辛(3mg/m²)和丝裂霉素(10mg/m²)均在每个疗程的第1天静脉推注(FEMi方案)。FEMi方案每3周重复一次,共进行三个疗程,之后每6周重复一次,直至疾病进展。63例患者中有13例(21%)出现主要客观缓解。另有12例患者(19%)出现轻微缓解。所有患者的中位生存期为23周,缓解患者的中位生存期为38周。治疗前的体能状态对缓解率和生存时间均有显著影响。初始卡氏评分大于或等于70%的患者缓解率为54%,缓解患者的中位生存期为42周。FEMi方案耐受性良好:18例患者(29%)未出现任何副作用,仅有5例(8%)出现呕吐。