Waldmann V, Goldschmidt H, Jäckel A, Deichmann M, Hegenbart U, Hartschuh W, Ho A, Näher H
Department of Dermatology, University of Heidelberg, Vossstr. 2, 69115 Heidelberg, Germany.
Br J Dermatol. 2000 Oct;143(4):837-9. doi: 10.1046/j.1365-2133.2000.03852.x.
Merkel cell carcinoma (MCC) is a rare cutaneous tumour with neuroendocrine differentiation. Metastasis occurs preferentially to regional lymph nodes but distant and multiple visceral metastases may occur. Chemotherapy has been performed with a variety of protocols based largely on agents active in small-cell lung cancer. Owing to the rarity of MCC, there is no standard protocol for the treatment of metastatic disease. We report a 59-year-old patient with systemic metastatic MCC. After diagnosis of distant metastases, first-line polychemotherapy (cisplatin 80 mg m(-2), doxorubicin 50 mg m(-2), etoposide 300 mg m(-2) and bleomycin 30 mg) was administered four times at 3-weekly intervals and resulted in partial remission of metastases. Subsequently, high-dose chemotherapy according to the PEI regimen (ifosfamide 12 g m(-2), carboplatin 900 mg m(-2) and etoposide 1500 mg m(-2)) was applied, followed by autologous blood stem cell transplantation (ABSCT). This protocol resulted in a complete remission that lasted for 6 months. This is the first report on a complete remission of metastatic MCC after high-dose polychemotherapy and ABSCT. High-dose chemotherapy might be a therapeutic option in chemosensitive metastatic MCC, and further evaluation is warranted.
默克尔细胞癌(MCC)是一种具有神经内分泌分化的罕见皮肤肿瘤。转移优先发生于区域淋巴结,但也可能发生远处和多发内脏转移。化疗已采用多种方案,主要基于对小细胞肺癌有效的药物。由于MCC罕见,对于转移性疾病的治疗尚无标准方案。我们报告一例59岁的系统性转移性MCC患者。在诊断为远处转移后,一线联合化疗(顺铂80mg/m²、阿霉素50mg/m²、依托泊苷300mg/m²和博来霉素30mg)每3周给药1次,共4次,结果转移灶部分缓解。随后,根据PEI方案进行大剂量化疗(异环磷酰胺12g/m²、卡铂900mg/m²和依托泊苷1500mg/m²),随后进行自体血干细胞移植(ABSCT)。该方案导致完全缓解持续6个月。这是关于大剂量联合化疗和ABSCT后转移性MCC完全缓解的首例报告。大剂量化疗可能是对化疗敏感的转移性MCC的一种治疗选择,值得进一步评估。