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高剂量异环磷酰胺联合美司钠静脉输注治疗晚期难治性肉瘤。

High-dose ifosfamide by infusion with Mesna in advanced refractory sarcomas.

作者信息

Güllü I, Yalçin S, Tekuzman G, Barişta I, Alkiş N, Celik I, Zengin N, Güler N, Kars A, Baltali E

机构信息

Hacettepe University, Institute of Oncology, Ankara, Turkey.

出版信息

Cancer Invest. 1996;14(3):239-42. doi: 10.3109/07357909609012146.

Abstract

Twenty patients with advanced sarcomas entered a pilot study with ifosfamide (IF) and mercaptoethane sulfonate sodium (Mesna) as a second-line treatment for six planned cycles. All patients had received prior doxorubicin- and cyclophosphamide-based chemotherapies. IF was administered at a dose of 3 g/m2 given as continuous intravenous infusion for 24 hr on day 1-5 with Mesna. In the absence of disease progression, chemotherapy was planned to be repeated every 4 weeks for six consecutive cycles. Following chemotherapy, only 2 patients (11%) achieved partial response with response durations of 6 and 9 months. There was no complete response. When considered for only high-grade tumors, the response rate reached up to 22%. Toxicity was reported for 48 cycles and the dose-limiting toxicities were myelosuppression (22%) and encephalopathy (17%). Chemotherapy protocol was changed after two or three courses in 16 patients with stable or progressive disease. IF/Mesna chemotherapy at this dose and schedule was not found to be very promising in refractory sarcomas as a second-line chemotherapy.

摘要

20例晚期肉瘤患者进入一项初步研究,使用异环磷酰胺(IF)和巯乙磺酸钠(美司钠,Mesna)作为二线治疗,计划进行六个周期。所有患者之前均接受过基于阿霉素和环磷酰胺的化疗。IF的给药剂量为3 g/m²,于第1 - 5天连续静脉输注24小时,并同时给予美司钠。在无疾病进展的情况下,计划每4周重复化疗,连续进行六个周期。化疗后,仅2例患者(11%)获得部分缓解,缓解持续时间分别为6个月和9个月。无完全缓解病例。仅考虑高级别肿瘤时,缓解率高达22%。共报告了48个周期的毒性反应,剂量限制性毒性为骨髓抑制(22%)和脑病(17%)。16例疾病稳定或进展的患者在两三个疗程后更改了化疗方案。IF/Mesna按此剂量和疗程进行化疗,作为难治性肉瘤的二线化疗,效果并不理想。

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