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108例既往未接受过化疗的转移性或不可切除肉瘤患者对美司钠、多柔比星、异环磷酰胺和达卡巴嗪的反应

Response to mesna, doxorubicin, ifosfamide, and dacarbazine in 108 patients with metastatic or unresectable sarcoma and no prior chemotherapy.

作者信息

Elias A, Ryan L, Sulkes A, Collins J, Aisner J, Antman K H

机构信息

Division of Medicine, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.

出版信息

J Clin Oncol. 1989 Sep;7(9):1208-16. doi: 10.1200/JCO.1989.7.9.1208.

Abstract

In this phase II trial, 105 eligible patients with no prior chemotherapy and advanced sarcoma received doxorubicin, ifosfamide, and dacarbazine (DTIC) with mesna uroprotection (MAID). Starting doses of these drugs were 60, 7,500, and 900 mg/m2 divided over 72 hours by continuous infusion, respectively. Mesna was given for 84 to 96 hours at 2,500 mg/m2/d. Myelosuppression was dose limiting, causing the only toxic death (sepsis). Nonhematologic toxicity consisted predominantly of anorexia and vomiting. Severe mucositis, macroscopic hematuria, renal tubular acidosis, renal failure, and CNS toxicity occurred in less than 5% of cycles. No cardiotoxicity was detected. The overall response rate (10% complete response [CR]) was 47% (95% confidence intervals, 5% to 18% and 37% to 57%, respectively). Most responses (approximately 70%) were observed within two cycles. Median times to progression were 10 and 9 months, respectively. Histologic high tumor grade, lesions less than 5 cm, and less than 1 year from diagnosis to study entry correlated with the probability of response. The median survival was 16 months. Time from diagnosis to study entry, performance status, and extent of disease, but not histologic grade, correlated with survival. Following CR, two patients remain disease-free at 32 and 16 months. Of the 15 additional patients rendered disease-free with surgery, two remain disease-free at 30 and 18 months with no further therapy. While most relapses occurred in sites of prior involvement, death from CNS metastases occurred in 11 of the 80 patients with high-grade sarcomas, of whom seven were still responding systematically (three complete responders). Because of its substantial response in this phase II trial, the MAID regimen is being compared with doxorubicin and DTIC alone in advanced sarcomas and to observation in the adjuvant treatment of high-grade sarcomas in randomized trials.

摘要

在这项II期试验中,105例未接受过化疗的晚期肉瘤合格患者接受了阿霉素、异环磷酰胺和达卡巴嗪(DTIC)联合美司钠尿路保护(MAID)治疗。这些药物的起始剂量分别为60、7500和900mg/m²,通过持续输注在72小时内给药。美司钠以2500mg/m²/天的剂量给药84至96小时。骨髓抑制是剂量限制性的,导致唯一的毒性死亡(败血症)。非血液学毒性主要包括厌食和呕吐。严重粘膜炎、肉眼血尿、肾小管酸中毒、肾衰竭和中枢神经系统毒性在不到5%的周期中发生。未检测到心脏毒性。总体缓解率(10%完全缓解[CR])为47%(95%置信区间分别为5%至18%和37%至57%)。大多数缓解(约70%)在两个周期内观察到。进展的中位时间分别为10个月和9个月。组织学高肿瘤分级、病变小于5cm以及从诊断到进入研究的时间小于1年与缓解概率相关。中位生存期为16个月。从诊断到进入研究的时间、体能状态和疾病范围与生存期相关,但组织学分级无关。CR后,两名患者分别在32个月和16个月时无疾病。在另外15例通过手术实现无疾病的患者中,两名患者在30个月和18个月时无疾病,无需进一步治疗。虽然大多数复发发生在先前受累部位,但80例高级别肉瘤患者中有11例死于中枢神经系统转移,其中7例仍有全身反应(3例完全缓解者)。由于其在这项II期试验中的显著反应,MAID方案正在与晚期肉瘤单独使用阿霉素和DTIC以及在随机试验中与高级别肉瘤辅助治疗中的观察进行比较。

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