Jett J R, Everson L, Therneau T M, Krook J E, Dalton R J, Marschke R F, Veeder M H, Brunk S F, Mailliard J A, Twito D I
Division of Medical Oncology, Mayo Clinic, Rochester, MN 55905.
J Clin Oncol. 1990 Jan;8(1):33-8. doi: 10.1200/JCO.1990.8.1.33.
In this randomized study involving patients with limited-stage small-cell lung cancer (LD-SCC), we compared treatment with either cyclophosphamide; doxorubicin, and vincristine (CAV) or CAV plus etoposide (CAVE). All patients received identical thoracic radiation consisting of 3,750 cGy in 15 fractions and prophylactic cranial radiation (3,000 cGy in 10 fractions). Among 231 evaluable patients, the two treatment arms were well matched with respect to sex, age, performance score, and presence or absence of heart disease. A major regression (REGR) was observed in 83% of all patients and a complete response (CR) in 60%. There was no difference in the response rate between the two treatment regimens. The median time to progression is 10.4 months (95% confidence interval [Cl], 8.9 to 12 months) for CAVE versus 8.9 months (95% Cl, 7.9 to 10.4 months) for CAV (P = .04). The median survival is 15.1 months (95% Cl, 11.7 to 17.8 months) for CAVE versus 12.4 months (95% Cl, 11 to 14.4 months) for CAV. This difference is not significantly different (P = .13). Toxicity was primarily myelosuppression and was significantly greater for the four-drug regimen. Fatal treatment-related toxicity was observed in two patients on the CAVE regimen and no treatment-related deaths were observed on the CAV treatment. In conclusion, the addition of etoposide to the CAV regimen resulted in increased toxicity but did not lead to a meaningful improvement in survival.
在这项针对局限期小细胞肺癌(LD-SCC)患者的随机研究中,我们比较了环磷酰胺、阿霉素和长春新碱(CAV)联合治疗与CAV加依托泊苷(CAVE)联合治疗的效果。所有患者均接受相同的胸部放疗,剂量为3750厘戈瑞,分15次进行,同时接受预防性脑放疗(3000厘戈瑞,分10次进行)。在231例可评估患者中,两个治疗组在性别、年龄、体能状态评分以及是否患有心脏病方面匹配良好。所有患者中有83%观察到主要缓解(REGR),60%观察到完全缓解(CR)。两种治疗方案的缓解率没有差异。CAVE组的中位进展时间为10.4个月(95%置信区间[Cl],8.9至12个月),而CAV组为8.9个月(95%Cl,7.9至10.4个月)(P = 0.04)。CAVE组的中位生存期为15.1个月(95%Cl,11.7至17.8个月),而CAV组为12.4个月(95%Cl,11至14.4个月)。这种差异无显著统计学意义(P = 0.13)。毒性主要为骨髓抑制,四药联合方案的毒性明显更大。在CAVE方案组有2例患者出现致命的治疗相关毒性,而CAV治疗组未观察到与治疗相关的死亡病例。总之,在CAV方案中加入依托泊苷会增加毒性,但并未导致生存期有显著改善。