白细胞介素-2体外活化杀伤细胞:晚期非小细胞肺癌的治疗。

Z P Bernstein, M H Goldrosen, L Vaickus, N Friedman, H Watanabe, R Rahman, J Park, S G Arbuck, J Sweeney, D S Vesper
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引用次数: 16

摘要

一项II期研究旨在检测白细胞介素-2 (IL-2)联合淋巴因子活化杀伤细胞(LAK)治疗晚期非小细胞肺癌(NSCLC)的疗效。IL-2以每天6 × 10(6) U/M2的固定剂量连续24小时静脉输注LAK细胞。11名患者参加了这项研究,其中6名可评估。一名患者在18个月的持续时间内几乎完全缓解。只有两名患者能够在不减少剂量的情况下完成疗程。该方案耐受性差,肺毒性是主要问题。部分应答者是唯一接受超过一个疗程治疗的患者。IL-2/LAK治疗可能在非小细胞肺癌中有活性,在这种一致致命的疾病中需要进一步的研究。然而,未来的研究将不得不纳入毒性较小的IL-2方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interleukin-2 with ex vivo activated killer cells: therapy of advanced non-small-cell lung cancer.

A phase II study was conducted to examine the efficacy of interleukin-2 (IL-2) with lymphokine-activated killer (LAK) cells as therapy for advanced non-small-cell lung carcinoma (NSCLC). IL-2 was administered at a fixed dose of 6 x 10(6) U/M2 per day as a 24 h continuous intravenous infusion (CIV) with LAK cells. Eleven patients were entered onto this study and six were evaluable. One patient had a near complete response of 18 months duration. Only two patients were able to complete the regimen without dose reduction. This regimen was poorly tolerated with pulmonary toxicity being the major problem. The partial responder was the only patient to undergo more than one course of therapy. IL-2/LAK therapy may have activity in NSCLC and further studies are warranted in this uniformly fatal disease. However, future studies will have to incorporate less toxic IL-2 regimens.

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