Merimsky O, Inbar M, Chaitchik S
Department of Oncology, Ichilov Hospital, Tel-Aviv, Israel.
Am J Clin Oncol. 1992 Feb;15(1):84-6. doi: 10.1097/00000421-199202000-00016.
Seventeen patients with histologically proven melanoma and measurable metastatic disease received 7-week cycles of fotemustine 100 mg/m2/day on days 1 and 8, and decarbazine (DTIC) 500 mg/m2/day on days 15 and 16, in a prospective open study, to assess the efficacy of fotemustine-DTIC combination. Response rate was 11.7%: one partial response (PR) in brain for 4.5 months, and one PR in brain and lymph nodes for 4 months. There was also one (5.8%) minimal response (MR) in brain, stomach, and lymph nodes for 8 months, and three (17.6%) patients with stable disease. Survival of responders was significantly superior to nonresponders. There was no response in brain without response in extracerebral sites. Toxicity was generally mild and well tolerated by all the patients. Fotemustine-DTIC showed some activity against metastatic melanoma, and should be further evaluated.
在一项前瞻性开放性研究中,17例经组织学证实为黑色素瘤且有可测量转移病灶的患者接受了为期7周的化疗周期,第1天和第8天给予福莫司汀100mg/m²/天,第15天和第16天给予达卡巴嗪(DTIC)500mg/m²/天,以评估福莫司汀 - DTIC联合用药的疗效。缓解率为11.7%:1例脑转移部分缓解(PR)持续4.5个月,1例脑和淋巴结转移PR持续4个月。还有1例(5.8%)脑、胃和淋巴结转移出现微小缓解(MR)持续8个月,3例(17.6%)患者病情稳定。缓解者的生存期明显优于未缓解者。脑内无转移而脑外部位无转移的患者无缓解情况。毒性一般较轻,所有患者耐受性良好。福莫司汀 - DTIC对转移性黑色素瘤显示出一定活性,应进一步评估。