Cohen M H, Ihde D C, Bunn P A, Fossieck B E, Matthews M J, Shackney S E, Johnston-Early A, Makuch R, Minna J D
Cancer Treat Rep. 1979 Feb;63(2):163-70.
Sixty-one protocol-eligible patients with small cell bronchogenic carcinoma received cyclic alternating combination chemotherapy with two or three non-cross-resistant drug combinations. No chest or prophylactic brain radiation therapy was used. Twenty-eight months after starting treatment, disease-free survival was 23% for patients achieving a complete response (CR) and 13% overall. Initial treatment consisted of high-dose cyclophosphamide, methotrexate, and CCNU (CMC) for 6 weeks. Patients then received vincristine, adriamycin, and procarbazine (VAP) for 6 weeks. The addition of VAP increased the CR rate from 42% to 74% in limited-disease patients and from 24% to 36% in extensive-disease patients. Half of the patients were randomized to a third combination of VO-16-213 and ifosfamide. These patients were cycled at 6-week intervals through the three drug regimens while the remaining patients were cycled between CMC and VAP. The addition of VP-16-213 and ifosfamide did not increase the CR rate or prolong survival. Only complete responders survived beyond 24 months. Sequential use of non-cross-resistant drug combinations represents one method for increasing the CR rate.
61例符合方案的小细胞支气管癌患者接受了两种或三种非交叉耐药药物组合的循环交替联合化疗。未进行胸部或预防性脑放射治疗。开始治疗28个月后,完全缓解(CR)患者的无病生存率为23%,总体无病生存率为13%。初始治疗包括高剂量环磷酰胺、甲氨蝶呤和洛莫司汀(CMC),为期6周。然后患者接受长春新碱、阿霉素和丙卡巴肼(VAP)治疗6周。在局限性疾病患者中,添加VAP使CR率从42%提高到74%,在广泛性疾病患者中从24%提高到36%。一半的患者被随机分配接受第三种组合,即依托泊苷-16-213和异环磷酰胺。这些患者每隔6周在三种药物方案之间循环,而其余患者在CMC和VAP之间循环。添加依托泊苷-16-213和异环磷酰胺并未提高CR率或延长生存期。只有完全缓解者存活超过24个月。序贯使用非交叉耐药药物组合是提高CR率的一种方法。