Di Re F, Bohm S, Oriana S, Spatti G B, Zunino F
Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
Cancer Chemother Pharmacol. 1990;25(5):355-60. doi: 10.1007/BF00686237.
Recent efforts to improve the response rates in advanced ovarian cancer with the use of high-dose cisplatin have been limited by unacceptable toxicity. Based on experimental and clinical studies indicating that reduced glutathione (GSH) is a protective agent against cisplatin-induced toxicity, a new high-dose regimen including GSH as a chemoprotector was designed in an attempt to improve the efficacy and therapeutic index of cisplatin. A total of 40 consecutive patients with stage III (bulky) and IV ovarian carcinoma were treated with cisplatin (40 mg/m2 daily for 4 consecutive days) and cyclophosphamide (600 mg/m2 i.v. on day 4). The treatment was repeated every 3-4 weeks for five courses unless progression or severe toxicity occurred. Before each cisplatin administration, patients received GSH (1,500 mg/m2) i.v. over 15 min, with a standard i.v. hydration (2,000 ml fluid) without diuretics. Debulking surgery was initially attempted in 18 patients and, after 2-3 courses, in 16 patients; it could not be carried out in 6 patients. Three patients were not evaluable for response because they prematurely discontinued their treatment. In all, 23 patients (62%) achieved complete clinical remission (negative second-look laparotomy in 16), with an overall (complete + partial) response rate of 86%; 2 patients achieved disease-free status following second surgery. Nausea/vomiting was the most severe acute toxic effect; myelosuppression was acceptable. Renal impairment was effectively prevented by GSH. Neurotoxicity that was not associated with motor dysfunction was the most significant cumulative toxicity in patients (24/32) receiving 4-5 courses. The results of this study indicate that the use of GSH is a safe new method for high-dose cisplatin administration. This regimen is well-tolerated and very effective in ovarian cancer patients with bulky disease and warrants further evaluation.
近期,使用高剂量顺铂提高晚期卵巢癌缓解率的努力因不可接受的毒性而受到限制。基于实验和临床研究表明还原型谷胱甘肽(GSH)是一种对抗顺铂诱导毒性的保护剂,设计了一种新的高剂量方案,包括使用GSH作为化学保护剂,试图提高顺铂的疗效和治疗指数。共有40例连续的III期(大块型)和IV期卵巢癌患者接受顺铂(每日40mg/m²,连续4天)和环磷酰胺(第4天静脉注射600mg/m²)治疗。除非病情进展或出现严重毒性,每3 - 4周重复治疗5个疗程。每次顺铂给药前,患者在15分钟内静脉输注GSH(1500mg/m²),同时进行标准的静脉补液(2000ml液体)且不使用利尿剂。最初对18例患者尝试进行减瘤手术,2 - 3个疗程后对16例患者进行了减瘤手术;6例患者无法进行手术。3例患者因过早停止治疗而无法评估疗效。总体而言,23例患者(62%)实现了完全临床缓解(16例二次剖腹探查阴性),总缓解率(完全缓解 + 部分缓解)为86%;2例患者在二次手术后达到无病状态。恶心/呕吐是最严重的急性毒性反应;骨髓抑制可接受。GSH有效预防了肾功能损害。在接受4 - 5个疗程治疗的患者中(24/32),与运动功能障碍无关的神经毒性是最显著的累积毒性。本研究结果表明,使用GSH是高剂量顺铂给药的一种安全新方法。该方案耐受性良好,对患有大块型疾病的卵巢癌患者非常有效,值得进一步评估。