接受重组白介素-2的晚期癌症患者化疗后体内白介素-2受体的表达降低。

Molecular biotherapy Pub Date : 1991-06-01
J Atzpodien, A Körfer, M Hadam, A Schomburg, T Menzel, I Dallmann, H Poliwoda, H Kirchner
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引用次数: 0

摘要

在我们机构进行的I/II期剂量递增研究中,共有14名晚期转移性癌症患者接受了4至16周的皮下重组白介素-2治疗。剂量以每周为间隔逐步增加,从180万IU/m2/天开始,直至每日1440万U/m2的最大剂量。当比较第0天(即IL-2之前)化疗前(n = 4)和未化疗前(n = 7)的患者时,两组患者外周血淋巴细胞均表现出相同水平的Tac IL-2受体(CD25)阳性(8%)。相比之下,4周的全身皮下il -2剂量递增治疗显示CD25细胞表面受体白介素-2的上调有显著差异。因此,连续治疗4周后,未接受化疗的患者外周血淋巴细胞CD25平均阳性为38%,而接受过化疗的患者为22% (p < 0.05)。这些数据表明,化疗预处理可能对体内对il -2的生物学反应有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Diminished expression of interleukin-2 receptors in vivo after prior chemotherapy in advanced cancer patients receiving recombinant interleukin-2.

In a phase I/II dose escalation study performed at our institution, a total of 14 advanced metastatic cancer patients received between 4 and 16 weeks of subcutaneous recombinant interleukin-2. Doses were escalated at weekly intervals, starting at 1.8 million IU/m2/day up to a maximum dose of 14.4 million U/m2 daily. When comparing patients with (n = 4) and without (n = 7) prior chemotherapy on day 0 (i.e., before rIL-2), both patient groups exhibited Tac IL-2 receptor (CD25) positive peripheral blood lymphocytes at equal levels of positivity (8%). In contrast, 4-week systemic treatment with subcutaneous rIL-2 at escalating dose levels revealed a significant difference in the up-regulation by interleukin-2 of CD25 cell surface receptor. Thus, after 4 consecutive weeks of treatment, patients without previous chemotherapy showed a mean CD25 positivity of peripheral blood lymphocytes at 38%, as compared with 22% in patients who did receive prior chemotherapy (p less than 0.05). These data suggest that chemotherapy pretreatment may have a significant effect on biological response to rIL-2 in vivo.

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