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美法仑和放线菌素D肢体隔离灌注治疗肢体局部黑色素瘤和软组织肉瘤:一项II期临床试验的最终报告

Isolated limb infusion with melphalan and dactinomycin for regional melanoma and soft-tissue sarcoma of the extremity: final report of a phase II clinical trial.

作者信息

Brady Mary S, Brown Karen, Patel Ami, Fisher Charles, Marx Will

机构信息

Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York 10065, USA.

出版信息

Melanoma Res. 2009 Apr;19(2):106-11. doi: 10.1097/CMR.0b013e32832985e3.

DOI:10.1097/CMR.0b013e32832985e3
PMID:19282789
Abstract

Isolated limb infusion (ILI) is a minimally invasive technique of delivering regional chemotherapy in patients with advanced melanoma or soft-tissue sarcoma of the limb. We report the final results of the first clinical trial of ILI in North America (NCT00004250). Eligible patients had recurrent melanoma or unresectable soft-tissue sarcoma of the limb. Angiographic catheters were positioned just above the knee or elbow of the extremity. General anesthesia was performed, a proximal tourniquet inflated, and a normothermic, low flow, hypoxic infusion of melphalan and dactinomycin circulated through the involved limb for 20 min. Tumor response and morbidity were assessed using standard criteria. Thirty-seven patients were accrued to the trial and 44 ILIs were performed (eight patients had two ILIs); one patient was not treated. Of the 32 evaluable patients, 17 (53%) had a significant response at 3 months: 25% of patients had a complete response and 28% of patients had a partial response. The median duration of complete response was 1 year (5-32 months). Morbidity was acceptable, with peak erythema, edema, and pain experienced at 2 weeks and considered 'moderate' in most patients. No patients developed compartment syndrome or required amputation because of ILI. ILI is well tolerated. More than half of the treated patients experienced a complete or partial response.

摘要

孤立肢体灌注(ILI)是一种为患有晚期肢体黑色素瘤或软组织肉瘤的患者提供区域化疗的微创技术。我们报告了北美首例ILI临床试验(NCT00004250)的最终结果。符合条件的患者患有复发性肢体黑色素瘤或不可切除的肢体软组织肉瘤。血管造影导管置于肢体膝盖或肘部上方。实施全身麻醉,近端止血带充气,美法仑和放线菌素的常温、低流量、低氧灌注液在受累肢体中循环20分钟。使用标准标准评估肿瘤反应和发病率。37名患者入组该试验,共进行了44次ILI(8名患者接受了两次ILI);1名患者未接受治疗。在32名可评估患者中,17名(53%)在3个月时出现显著反应:25%的患者完全缓解,28%的患者部分缓解。完全缓解的中位持续时间为1年(5 - 32个月)。发病率可接受,大多数患者在2周时出现的红斑、水肿和疼痛峰值被认为是“中度”。没有患者因ILI发生骨筋膜室综合征或需要截肢。ILI耐受性良好。超过一半的接受治疗的患者出现了完全或部分缓解。

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