Vuoristo M S, Gröhn P, Kellokumpu-Lehtinen P, Kumpulainen E, Turunen M, Korpela M, Joensuu H, Tiusanen K, Nevantaus A
Department of Clinical Medicine, University of Tampere, Finland.
J Cancer Res Clin Oncol. 1995;121(3):175-80. doi: 10.1007/BF01198100.
This study was conducted to evaluate the efficacy and the tolerability of a four-drug chemotherapy regimen combined with interferon alpha (IFN) in metastatic melanoma. Between March 1991 and August 1993, 55 patients with advanced melanoma were enrolled for the present multicentre phase II study. Forty-nine patients were eligible and evaluable for toxicity; 48 patients were evaluable for response. The treatment schedule consisted of a 5-day regimen of dacarbazine, vincristine, bleomycin and lomustine, plus 6 x 10(6) IU IFN alpha three times weekly subcutaneously for 2 weeks starting on day 8. The cycle was repeated on day 29. Among the 48 assessable patients, 16 objective responses were seen, yielding a response rate of 33% (95% confidence interval 20%-46%). Seven patients achieved a complete response (CR) of a median of 6+ months (range 1+ to 21+ months) and 9 patients achieved a partial response (PR) of a median of 9 months (range 4-13 months). The median overall survival was 12+ months (range 6+ to 23+ months) for the patients with CR and 15+ months (range 8-20 months) for the patients with PR. Even the survival of the 7 patients with stable disease was fairly long (median 12, range 7-17 months), appearing to be significantly longer than the survival of the 25 patients with progressive disease (median 5, range 1-24+ months). The treatment was moderately well tolerated, although all patients experienced some mild form of toxicity, mostly gastrointestinal symptoms, neurotoxicity and haematotoxicity. Grade 3-4 adverse effects were noted in 39% of the patients. No toxic deaths occurred. It can be concluded that the present regimen produces meaningful responses for patients with metastatic melanoma. A randomised study is needed to determine the effect on survival.
本研究旨在评估一种四联化疗方案联合α干扰素(IFN)治疗转移性黑色素瘤的疗效和耐受性。1991年3月至1993年8月,55例晚期黑色素瘤患者入选本多中心II期研究。49例患者符合毒性评估标准且可进行评估;48例患者可进行疗效评估。治疗方案包括达卡巴嗪、长春新碱、博来霉素和洛莫司汀的5天疗程,加用6×10⁶IU α干扰素,从第8天开始每周皮下注射3次,共2周。第29天重复周期。在48例可评估患者中,观察到16例客观缓解,缓解率为33%(95%置信区间20%-46%)。7例患者达到完全缓解(CR),中位缓解时间为6+个月(范围1+至21+个月),9例患者达到部分缓解(PR),中位缓解时间为9个月(范围4-13个月)。CR患者的中位总生存期为12+个月(范围6+至23+个月),PR患者为15+个月(范围8-20个月)。即使是7例病情稳定患者的生存期也相当长(中位12个月,范围7-17个月),似乎明显长于25例病情进展患者的生存期(中位5个月,范围1-24+个月)。该治疗耐受性中等良好,尽管所有患者均经历了某种轻度毒性反应,主要是胃肠道症状、神经毒性和血液毒性。39%的患者出现3-4级不良反应。未发生毒性死亡。可以得出结论,本方案对转移性黑色素瘤患者产生了有意义的缓解。需要进行一项随机研究以确定对生存期的影响。