Aisner J, Whitacre M, VanEcho D A, Wesley M, Wiernik P H
Cancer Chemother Pharmacol. 1982;7(2-3):187-93. doi: 10.1007/BF00254546.
Small cell lung cancer requires aggressive combination chemotherapy. The three active agents, doxorubicin (A) 45 mg/m2 i.v. day 1, cyclophosphamide (C) 1.0 mg/m2 i.v. day 1 and VP16-213 (E) 50 mg/m2/day i.v. days 1-5 were given together. The combination (ACE) was given every 21 days without chest irradiation. One hundred and seventy-four patients have been stratified for extent of disease and randomized on three sequential studies testing ACE vs ACE + MER immunotherapy (38 patients), or ACE vs ACE alternating with CCNU, methotrexate, vincristine and procarbazine (109 patients), or ACE vs ACE II (ACE with continuous VP16-213 - 100 mg/m2/day X 5 days - 27 patients - ongoing). The immunotherapy and the alternating non-cross resistant combination have not proven beneficial with respect to response or survival. The ACE combination, regardless of additional treatments, has produced greater than 90% response overall. In limited disease the complete response (CR) frequency is 65%. The median survival for limited disease overall is 14 months and 18 months for patients achieving CR. In extensive disease the CR frequency is 40% with a median survival of 9 months overall and 13 months for patients achieving CR. Response frequency and survival are identical in the first two studies and 20-30% of patients with limited disease are long-term survivors with one late relapse (greater than 3 years). Patients who achieved CR had a significantly longer survival regardless of other factors such as performance status or extent of disease. Prophylactic cranial irradiation was demonstrated to be useful in prevention or delaying CNS metastases in patients who achieved CR. The third generation study of high-dose VP16-213 infusion seeks to increase the CR frequency. ACE chemotherapy without chest irradiation is a highly effective treatment for all patients with small cell lung cancer and compares favorably with all other studies with or without adjuvant radiotherapy.
小细胞肺癌需要积极的联合化疗。三种活性药物,阿霉素(A)45毫克/平方米静脉注射第1天,环磷酰胺(C)1.0毫克/平方米静脉注射第1天,以及依托泊苷(E)50毫克/平方米/天静脉注射第1 - 5天,一起给药。联合方案(ACE)每21天给药一次,不进行胸部放疗。174例患者根据疾病范围进行分层,并随机分为三项连续研究,分别测试ACE与ACE + MER免疫疗法(38例患者),或ACE与交替使用洛莫司汀、甲氨蝶呤、长春新碱和丙卡巴肼的ACE方案(109例患者),或ACE与ACE II方案(持续使用依托泊苷 - 100毫克/平方米/天×5天 - 27例患者 - 正在进行)。免疫疗法和交替使用的非交叉耐药联合方案在反应或生存方面尚未证明有益。ACE联合方案,无论是否有其他治疗,总体有效率均超过90%。在局限性疾病中,完全缓解(CR)频率为65%。局限性疾病总体的中位生存期为14个月,达到CR的患者为18个月。在广泛期疾病中,CR频率为40%,总体中位生存期为9个月,达到CR的患者为13个月。前两项研究中的反应频率和生存期相同,20 - 30%的局限性疾病患者为长期幸存者,有1例晚期复发(超过3年)。达到CR的患者生存期显著更长,无论其他因素如体能状态或疾病范围如何。预防性颅脑照射被证明对预防或延迟达到CR的患者发生中枢神经系统转移有用。高剂量依托泊苷输注的第三代研究旨在提高CR频率。不进行胸部放疗的ACE化疗是所有小细胞肺癌患者的高效治疗方法,与所有其他有或没有辅助放疗的研究相比具有优势。