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一种基于自体淋巴因子激活的杀伤细胞和重组白细胞介素-2全身给药的癌症治疗新方法。

A new approach to the therapy of cancer based on the systemic administration of autologous lymphokine-activated killer cells and recombinant interleukin-2.

作者信息

Rosenberg S A, Lotze M T, Muul L M, Leitman S, Chang A E, Vetto J T, Seipp C A, Simpson C

出版信息

Surgery. 1986 Aug;100(2):262-72.

PMID:3526604
Abstract

A new approach to cancer therapy has been developed based on the adoptive transfer of autologous lymphokine-activated killer (LAK) cells and recombinant interleukin-2 (IL-2). Forty-one patients with advanced cancer who have failed all standard treatments were treated in this experimental protocol. Fourteen patients experienced an objective regression of cancer, including one patient with metastatic melanoma who underwent a complete regression. Objective responses were seen in patients with colorectal cancer, renal cell cancer, melanoma, and lung adenocarcinoma. The sites of tumor regression included subcutaneous tissue, lung, and liver. The major side effect of therapy resulted from the administration of high-dose IL-2 and was manifested primarily as fluid retention, resulting in a generalized capillary permeability leak syndrome. This approach to adoptive immunotherapy represents a promising approach to the therapy of patients with metastatic cancer. Attempts to increase the potency and decrease the toxicity of therapy and extend this treatment to patients with smaller tumor burdens are in progress.

摘要

基于自体淋巴因子激活的杀伤细胞(LAK)和重组白细胞介素-2(IL-2)的过继性转移,已开发出一种新的癌症治疗方法。41例对所有标准治疗均无效的晚期癌症患者按此实验方案进行治疗。14例患者出现癌症客观缓解,其中1例转移性黑色素瘤患者完全缓解。在结直肠癌、肾细胞癌、黑色素瘤和肺腺癌患者中观察到客观缓解。肿瘤消退部位包括皮下组织、肺和肝。治疗的主要副作用源于高剂量IL-2的给药,主要表现为液体潴留,导致全身性毛细血管通透性渗漏综合征。这种过继性免疫疗法是治疗转移性癌症患者的一种有前景的方法。目前正在努力提高治疗效力、降低毒性,并将这种治疗方法扩展到肿瘤负荷较小的患者。

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