首页> 外文期刊>Oncology reports >Hyperthermic isolated limb perfusion for recurrent melanomas and soft tissue sarcomas: feasibility and reproducibility in a multi-institutional Hellenic collaborative study.
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Hyperthermic isolated limb perfusion for recurrent melanomas and soft tissue sarcomas: feasibility and reproducibility in a multi-institutional Hellenic collaborative study.

机译:高温隔离肢体灌注治疗复发性黑色素瘤和软组织肉瘤:在多机构希腊合作研究中的可行性和可重复性。

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摘要

Hyperthermic isolated limb perfusion with TNF-alpha and melphalan (TM-HILP) is a complicated surgical procedure. Herein, we present the experience of the Hellenic collaborating centers with TM-HILP for inoperable in-transit melanoma and soft tissue sarcoma (STS) of the extremities to examine safety and feasibility of collaborating as a multi-institutional group for future research studies. From 2001 to 2009, twenty patients (median age 63.5 years) underwent TM-HILP for locally advanced in-transit melanoma (n=14) or unresectable STS (n=6). All patients underwent a 90-min isolated limb perfusion with melphalan (10 mg/l limb volume) and TNF-alpha (1-2 mg) under mild hyperthermia (39-40 degrees C). No major intra-operative complications occurred and all patients completed the procedure successfully. One patient developed postoperative ischemic necrosis of the limb necessitating amputation. All melanoma patients showed a response to TM-HILP with 7 (62%) of them experiencing complete response. All STS patients attained complete response after excision of residual tumor. The median disease specific and limb-relapse-free survival was 15 and 12 months, respectively. TM-HILP can be safely applied even in low volume tertiary hospitals provided that technology to minimize intraoperative systemic leakage is available. Future prospective studies can be performed reproducibly by this multi-institutional collaborative group.
机译:TNF-α和美法仑(TM-HILP)的高温离体肢体灌注是一个复杂的手术过程。在这里,我们介绍与TM-HILP开展的希腊协作中心在无法手术的四肢黑色素瘤和四肢软组织肉瘤(STS)方面的经验,以检查作为多机构协作进行协作的安全性和可行性,以进行未来的研究。从2001年到2009年,二十名患者(中位年龄为63.5岁)因局部进展中转黑色素瘤(n = 14)或无法切除的STS(n = 6)接受了TM-HILP治疗。在温和的高温(39-40摄氏度)下,所有患者均进行了90分钟的肢体灌注,分别为美法仑(肢体体积为10 mg / l)和TNF-α(1-2 mg)。没有发生重大的术中并发症,所有患者均成功完成了手术。一名患者发生肢体缺血性坏死,需要截肢。所有黑色素瘤患者均显示出对TM-HILP的反应,其中7(62%)患者完全反应。切除残留肿瘤后,所有STS患者均获得完全缓解。中位疾病特异性生存和无肢体复发生存分别为15个月和12个月。 TM-HILP即使在小容量的三级医院中也可以安全地应用,只要可以使用使术中系统性渗漏最小化的技术即可。这个多机构协作小组可以重复进行未来的前瞻性研究。

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