Gurney H, Coates A, Kefford R
Department of Medicine, University of Sydney Westmead Centre, Australia.
J Invest Dermatol. 1991 Jan;96(1):85-7. doi: 10.1111/1523-1747.ep12515896.
A combination of L-dopa and carbidopa was given orally to 17 patients with metastatic melanoma. Maximum tolerated oral doses were given, up to 4 grams daily. No response was seen in 15 patients evaluable for response. Toxicity was considerable, with seven of 17 patients (41%) stopping treatment because of unacceptable gastrointestinal toxicity or postural hypotension. Contrary to previous anecdotal reports, there was no evidence that L-dopa/carbidopa treatment resulted in accelerated progression of metastatic melanoma. Orally administered L-dopa/carbidopa is ineffective as therapy for advanced melanoma when maximum tolerated doses are used.
将左旋多巴和卡比多巴联合口服给予17例转移性黑色素瘤患者。给予最大耐受口服剂量,每日最高达4克。15例可评估反应的患者未见反应。毒性相当大,17例患者中有7例(41%)因无法接受的胃肠道毒性或体位性低血压而停止治疗。与之前的轶事报道相反,没有证据表明左旋多巴/卡比多巴治疗会导致转移性黑色素瘤进展加速。当使用最大耐受剂量时,口服左旋多巴/卡比多巴作为晚期黑色素瘤的治疗方法无效。