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肿瘤坏死因子(TNF)在离体灌注中的应用:结果与副作用。美国国立癌症研究所的结果。

The use of tumour necrosis factor (TNF) in isolated perfusion: results and side effects. The NCI results.

作者信息

Fraker D L, Alexander H R

机构信息

Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Melanoma Res. 1994 Mar;4 Suppl 1:27-9.

PMID:8038592
Abstract

The Surgery Branch of the National Cancer Institute has initiated several clinical trials involving the use of high-dose TNF in isolated limb perfusions. A phase III trial compares the three drug combination of TNF, interferon-gamma (IFN-gamma) and melphalan with a standard melphalan-alone perfusion in a prospective randomized trial. Another protocol escalates the dose of TNF in the perfusate to define the maximally tolerated dose that can be administered in this regional manner. A third protocol adds systemic high-dose interleukin-2 postoperatively to a TNF, IFN, and melphalan limb perfusion for patients with stage IV melanoma with the bulk of the disease in the extremity. This brief review highlights the rationale and study design of these TNF limb perfusion protocols.

摘要

美国国立癌症研究所外科分部已开展了多项关于在肢体隔离灌注中使用高剂量肿瘤坏死因子(TNF)的临床试验。一项III期试验在前瞻性随机试验中,将TNF、γ干扰素(IFN-γ)和马法兰的三联药物组合与标准的单纯马法兰灌注进行比较。另一项方案提高灌注液中TNF的剂量,以确定能以这种局部方式给药的最大耐受剂量。第三个方案是,对于疾病主要位于肢体的IV期黑色素瘤患者,在TNF、IFN和马法兰肢体灌注术后添加全身高剂量白细胞介素-2。本简要综述重点介绍了这些TNF肢体灌注方案的基本原理和研究设计。

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