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标准剂量与剂量强化的阿霉素、异环磷酰胺和达卡巴嗪(MAID)用于转移性和局部晚期软组织肉瘤一线治疗的III期试验

Phase III trial of standard versus dose-intensified doxorubicin, ifosfamide and dacarbazine (MAID) in the first-line treatment of metastatic and locally advanced soft tissue sarcoma.

作者信息

Fayette Jérôme, Penel Nicolas, Chevreau Christine, Blay Jean-Yves, Cupissol Didier, Thyss Antoine, Guillemet Cécile, Rios Maria, Rolland Frédéric, Fargeot Pierre, Bay Jacques Olivier, Mathoulin-Pelissier Simone, Coindre Jean Michel, Bui-Nguyen Binh

机构信息

Centre Léon Bérard, Département de Médecine & Inserm U590, Université de Lyon, 28 rue Laennëc, 69008, Lyon, France.

出版信息

Invest New Drugs. 2009 Oct;27(5):482-9. doi: 10.1007/s10637-008-9217-1. Epub 2009 Jan 16.

Abstract

Multidrug chemotherapy increases responses in advanced soft tissues sarcoma. Can a 20% increase of relative dose intensity of the MAID regimen, more improve responses? From 1994 to 1997, 162 patients were randomized in a phase III study to the conventional drug combination (6 cycles of MAID: 60, 7,500, 900 mg/m(2) for doxorubicin, ifosfamide and dacarbazine respectively), or at doses 20-33% higher per cycle (5 cycles of intensified MAID for similar cumulative doses) with systematic G-CSF. Primary endpoint was response rate; secondary were toxicity, event-free and overall survival. The objective response rate in assessable patients was 38% with intensified MAID and 35% with MAID (p = 0.72). Event-free and overall survivals were similar in both arms. Only grade 3-4 thrombocytopenia and anemia were significantly higher in intensified arm. Treatment with intensified MAID did not improve response rate neither survival and cannot be recommended for advanced or metastatic soft tissue sarcoma.

摘要

多药化疗可提高晚期软组织肉瘤的缓解率。MAID方案相对剂量强度增加20%能否进一步提高缓解率?1994年至1997年,162例患者在一项III期研究中被随机分为接受传统药物联合方案(6个周期的MAID:阿霉素、异环磷酰胺和达卡巴嗪的剂量分别为60、7500、900mg/m²),或每个周期剂量高20%-33%(5个周期的强化MAID,累积剂量相似)并系统性使用粒细胞集落刺激因子(G-CSF)。主要终点是缓解率;次要终点是毒性、无事件生存期和总生存期。可评估患者中,强化MAID组的客观缓解率为38%,MAID组为35%(p = 0.72)。两组的无事件生存期和总生存期相似。仅强化组3-4级血小板减少症和贫血显著更高。强化MAID治疗既未提高缓解率也未改善生存期,不推荐用于晚期或转移性软组织肉瘤。

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