Department of Dermatology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
J Dermatol. 2011 Feb;38(2):164-8. doi: 10.1111/j.1346-8138.2010.00947.x. Epub 2010 Nov 11.
Therapy-related myelodysplastic syndrome (t-MDS) is mostly attributed to chemotherapeutic agents of alkylating agents. Few studies have evaluated the late effects of chemotherapy for malignant melanoma (MM). To evaluate whether dacarbazine, nimustine hydrochloride and vincristine sulfate (DAV) therapy for MM related to t-MDS or not, a retrospective analysis was performed. We conducted a retrospective case-control study in a cohort of the 217 patients diagnosed with MM from 1989-2007 in Aichi Medical University Department of Dermatology and Nagoya University Graduate School of Medicine Department of Dermatology. One hundred and fifty-five of the 217 patients with MM were prospectively followed after DAV therapy or with or without local injection of β-interferon, of whom two patients developed t-MDS. Cytogenetic abnormalities were found in two of the 35 patients by chromosome banding method - leukemia (G-Banding). The karyotypes were found in the chromosome of -5, deletion (5), addition (7) and 7q-. In conclusion, DAV therapy should be used carefully for older patients with MM after satisfactory operation.
治疗相关性骨髓增生异常综合征(t-MDS)主要归因于烷化剂类化疗药物。很少有研究评估过化疗治疗恶性黑色素瘤(MM)的晚期效应。为了评估达卡巴嗪、盐酸尼莫司汀和硫酸长春新碱(DAV)治疗是否与 t-MDS 相关,我们进行了一项回顾性分析。我们在爱知医科大学皮肤科和名古屋大学研究生院皮肤科诊断为 MM 的 217 例患者队列中进行了回顾性病例对照研究。155 例 MM 患者接受 DAV 治疗或联合或不联合β干扰素局部注射后进行前瞻性随访,其中 2 例发生 t-MDS。通过染色体带法 - 白血病(G 带)在 35 例患者中的 2 例中发现细胞遗传学异常。核型在染色体 -5、缺失(5)、添加(7)和 7q-中发现。总之,对于满意手术治疗后的老年 MM 患者,应谨慎使用 DAV 治疗。