Joensuu H
Department of Radiotherapy and Oncology, Turku University Central Hospital, Finland.
Br J Cancer. 1991 Jan;63(1):154-6. doi: 10.1038/bjc.1991.32.
Fifty-five evaluable patients with disseminated malignant melanoma were treated with the combination of dacarbazine (DTIC) 400 mg i.v. on days 1 to 3 and lomustine (CCNU) 50 to 80 mg m-2 orally on day 1 with intervals of 6 weeks as the first line chemotherapy. Three (5%) patients had complete and 6 (11%) partial response, and 7 (13%) patients had stable disease at least for 3 months. The patients with an objective response (n = 9) survived longer than the rest of the patients if the length of survival was calculated from the start of chemotherapy (P = 0.0006). However, the responding patients also had longer time interval from the diagnosis to the detection of distant metastases (P = 0.05), and survival time from disease progression following DTIC and CCNU therapy (P = 0.005). These findings suggest that patients with an objective response to DTIC-CCNU therapy have melanoma with a slow progression rate, and prolonged survival in such patients may in part result from the less aggressive biological nature of their tumours.
55例可评估的播散性恶性黑色素瘤患者接受了一线化疗,方案为第1至3天静脉注射达卡巴嗪(DTIC)400mg,第1天口服洛莫司汀(CCNU)50至80mg/m²,每6周为一个周期。3例(5%)患者完全缓解,6例(11%)部分缓解,7例(13%)患者疾病稳定至少3个月。如果从化疗开始计算生存时间,客观缓解的患者(n = 9)比其余患者存活时间更长(P = 0.0006)。然而,缓解患者从诊断到发现远处转移的时间间隔也更长(P = 0.05),以及从DTIC和CCNU治疗后疾病进展开始计算的生存时间也更长(P = 0.005)。这些发现表明,对DTIC-CCNU治疗有客观缓解的患者所患黑色素瘤进展速度较慢,此类患者生存时间延长可能部分归因于其肿瘤侵袭性较低的生物学特性。