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首页> 外文期刊>Melanoma research >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.
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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.

机译:肢体局部输注美法仑和放线菌素治疗区域性黑色素瘤和四肢软组织肉瘤:II期临床试验的最终报告。

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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.
机译:肢体孤立输注(ILI)是一种微创技术,可在患有晚期黑素瘤或肢体软组织肉瘤的患者中进行局部化疗。我们报告了ILI在北美的首次临床试验(NCT00004250)的最终结果。符合条件的患者患有复发性黑色素瘤或肢体不可切除的软组织肉瘤。血管造影导管正好位于四肢的膝盖或肘部上方。进行全身麻醉,向近端止血带充气,并通过受累肢体循环正常,低流量,低氧输注马法兰和放线菌素20分钟。使用标准标准评估肿瘤反应和发病率。该试验共纳入37位患者,并进行了44次ILI(8位患者有2次ILI);一名患者未接受治疗。在32例可评估患者中,有17例(53%)在3个月时有明显缓解:25%的患者完全缓解,28%的患者部分缓解。完全缓解的中位数持续时间为1年(5-32个月)。发病率可接受,在2周时出现红斑,浮肿和疼痛高峰,在大多数患者中被认为是“中度”的。没有患者因ILI发生隔室综合征或需要截肢。 ILI的耐受性良好。超过一半的接受治疗的患者经历了完全或部分反应。

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