Perez C A, Einhorn L, Oldham R K, Greco F A, Cohen H J, Silberman H, Krauss S, Hornback N, Comas F, Omura G
J Clin Oncol. 1984 Nov;2(11):1200-8. doi: 10.1200/JCO.1984.2.11.1200.
A total of 304 patients with limited small-cell carcinoma of the lung were treated with a combination of cyclophosphamide, Adriamycin (Adria Laboratories, Columbus, Ohio), and vincristine (CAV) and elective brain irradiation (3,600 rad TD in 14 fractions). The patients were randomized to either receive or not receive thoracic irradiation (4,000 rad TD, split course). Of the 304 patients, 291 were eligible for the study. Two hundred eighteen (75%) were completely evaluable. In each group, 81% of the patients had a Karnofsky index of 80% or higher and 14% had supraclavicular or scalene lymph nodes. Patients treated with CAV and no thoracic irradiation had a complete response (CR) of 48%, in contrast to 63% for those receiving chest irradiation (P = .05). In the first group, the complete and partial response rate was 70%; in the second, 80%. The median survival for the eligible patients treated with CAV and brain radiation therapy was 49 weeks; for those treated with the same regimen plus thoracic irradiation, the median survival was 60 weeks. The actuarial two-year tumor-free survival is 19% in the first group and 28% in the second group. The median survival for the responders in the CAV plus brain irradiation group was 57 weeks and for those receiving thoracic irradiation, 78 weeks (P = .12). Thoracic failure was 52% in patients not treated with thoracic radiation therapy v 36% in those receiving it (P = .06). The distant metastases incidence was 23% in patients not treated with thoracic radiation and 35% in patients treated with thoracic radiation. Hematologic toxicity was comparable in both groups; 30% of the patients had moderate to severe granulocytopenia and 6%, low homoglobin. Two toxicity-related deaths occurred (one in each group). Moderate gastrointestinal toxicity was noted in 41% and severe in 16% of the patients receiving CAV and brain irradiation without thoracic radiotherapy v 44% and 20% in those irradiated in the thorax. Disease-free survival is enhanced in the patients receiving thoracic irradiation. More effective chemotherapy is critically needed to significantly improve overall survival. These preliminary results suggest that thoracic irradiation should be a primary component in the therapy of these patients, although this combined therapy is moderately toxic.(ABSTRACT TRUNCATED AT 400 WORDS)
共有304例局限性肺小细胞癌患者接受了环磷酰胺、阿霉素(阿德里亚实验室,俄亥俄州哥伦布市)和长春新碱(CAV)联合治疗以及选择性脑照射(14次分割,总量3600拉德)。患者被随机分为接受或不接受胸部照射(总量4000拉德,分程照射)。304例患者中,291例符合研究条件。218例(75%)可进行全面评估。每组中,81%的患者卡氏评分在80%及以上,14%有锁骨上或斜角肌淋巴结转移。接受CAV且未进行胸部照射的患者完全缓解(CR)率为48%,而接受胸部照射的患者为63%(P = 0.05)。第一组中,完全缓解和部分缓解率为70%;第二组为80%。接受CAV和脑放射治疗的符合条件患者的中位生存期为49周;接受相同方案加胸部照射的患者,中位生存期为60周。第一组的两年无瘤生存率为19%,第二组为28%。CAV加脑照射组缓解患者的中位生存期为57周,接受胸部照射的患者为78周(P = 0.12)。未接受胸部放射治疗的患者胸部失败率为52%,接受胸部放射治疗的患者为36%(P = 0.06)。未接受胸部放射治疗的患者远处转移发生率为23%,接受胸部放射治疗的患者为35%。两组血液学毒性相当;30%的患者有中度至重度粒细胞减少,6%有低血红蛋白。发生了两例与毒性相关的死亡(每组各一例)。接受CAV和脑照射但未进行胸部放疗的患者中,41%有中度胃肠道毒性,16%有重度胃肠道毒性;接受胸部照射的患者中,这一比例分别为44%和20%。接受胸部照射的患者无病生存期延长。急需更有效的化疗以显著提高总体生存率。这些初步结果表明,胸部照射应是这些患者治疗的主要组成部分,尽管这种联合治疗有中度毒性。(摘要截选至400字)