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用链脲佐菌素、环己亚硝脲、阿霉素和博来霉素对先前接受过治疗的晚期霍奇金病进行联合化疗。

Combination chemotherapy of advanced previously treated Hodgkin's disease with streptozotocin, CCNU, adriamycin and bleomycin.

作者信息

Levi J A, Wiernik P H, Diggs C H

出版信息

Med Pediatr Oncol. 1977;3(1):33-40. doi: 10.1002/mpo.2950030106.

Abstract

Seventeen patients with advanced, previously treated Hodgkin's disease received therapy with a combination of streptozotocin 500 mg/m2/day i.v. days 1--5, CCNU 100 mg/m2 orally day 1, adriamycin 45 mg/m2 i.v. day 1, and bleomycin 15 mg/m2 i.m. days 1 and 8 at 28-day intervals (SCAB). The overall response rate was 59% with six patients (35%) achieving complete remission and four patients (24%) entering partial remissions. No maintenance therapy was given and the median duration of complete remission was 8+ months (range 2+-18+ months), while the median duration of partial remission was only 2 months (range 2-3 months). The median duration of survival from the start of therapy for the complete responders was 16+ months (range 5+-25+ months) while the median survival for the partial and nonresponders was only 5 months (range 2-13 and 3-11+ months, respectively). Toxicity was a major problem with this drug combination. Myelosuppression occurred regularly and was severe after 25% of courses. There were two deaths directly related to drug-induced myelosuppression. Other serious toxicities included bleomycin-induced pulmonary toxicity in three patients, with one death; renal tubular dysfunction secondary to streptozotocin in three patients; hepatic dysfunction in three patients and severe weight loss in three. SCAB has proven to be an active although toxic combination which is not cross-resistant to MOPP-type regimens. Alterations in drug dosages and scheduling are being evaluated in an effect to ameliorate toxicity and preserve efficacy.

摘要

17例晚期霍奇金病患者,此前均接受过治疗,接受了链脲佐菌素(500mg/m²/天,静脉注射,第1 - 5天)、环己亚硝脲(100mg/m²,口服,第1天)、阿霉素(45mg/m²,静脉注射,第1天)和博来霉素(15mg/m²,肌肉注射,第1天和第8天)联合治疗,每28天为一个疗程(SCAB方案)。总缓解率为59%,6例患者(35%)达到完全缓解,4例患者(24%)进入部分缓解。未给予维持治疗,完全缓解的中位持续时间为8 +个月(范围2 + - 18 +个月),而部分缓解的中位持续时间仅为2个月(范围2 - 3个月)。完全缓解者从治疗开始的中位生存期为16 +个月(范围5 + - 25 +个月),而部分缓解者和未缓解者的中位生存期仅为5个月(分别为2 - 13个月和3 - 11 +个月)。毒性是这种药物组合的一个主要问题。骨髓抑制经常发生,25%的疗程后严重。有2例死亡与药物引起的骨髓抑制直接相关。其他严重毒性包括3例患者出现博来霉素引起的肺部毒性,其中1例死亡;3例患者因链脲佐菌素继发肾小管功能障碍;3例患者出现肝功能障碍,3例患者出现严重体重减轻。SCAB方案已被证明是一种有效的但有毒的组合,对MOPP方案无交叉耐药性。正在评估药物剂量和给药方案的改变,以减轻毒性并保持疗效。

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