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头颈部晚期鳞状细胞癌患者瘤周及瘤内注射白细胞介素-2疗效的Ib期试验:一项东部肿瘤协作组试验

Phase Ib trial of the effect of peritumoral and intranodal injections of interleukin-2 in patients with advanced squamous cell carcinoma of the head and neck: an Eastern Cooperative Oncology Group trial.

作者信息

Vlock D R, Snyderman C H, Johnson J T, Myers E N, Eibling D E, Rubin J S, Kirkwood J M, Dutcher J P, Adams G L

机构信息

Department of Medicine, Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pennsylvania.

出版信息

J Immunother Emphasis Tumor Immunol. 1994 Feb;15(2):134-9. doi: 10.1097/00002371-199402000-00007.

Abstract

Thirty-six patients with unresectable squamous cell carcinoma of the head and neck were entered into a phase Ib trial evaluating the toxicity, maximally tolerated dose (MTD), and immunomodulating effects of locally administered interleukin-2 (IL-2). Patients received daily IL-2 injected perilesionally in divided doses in each of four quadrants and bilaterally into the superior jugular lymph nodes. The dose of IL-2 began at 200 U/day and was escalated to 4 x 10(6) U/day in groups of six patients. Overall, regionally administered IL-2 was well tolerated. The most frequently encountered toxicities were fever, hepatotoxicity, and hypotension. Dose-limiting toxicity was encountered at 4 x 10(6) U. Of the 36 patients treated, 2 partial responses were noted at 2,000 and 4 x 10(6) U. We conclude that regionally administered IL-2 is well tolerated in patients with head and neck cancer and that the MTD is 2 x 10(6) U/day, similar to what has been reported with systemically administered IL-2. Although the overall response rate was low, it may be improved with prolonged administration of IL-2 or by combining it with other biologic or cytotoxic agents.

摘要

36例不可切除的头颈部鳞状细胞癌患者进入一项Ib期试验,评估局部给予白细胞介素-2(IL-2)的毒性、最大耐受剂量(MTD)和免疫调节作用。患者每日在四个象限分别以分剂量在病变周围注射IL-2,并双侧注射到颈上淋巴结。IL-2的剂量从200 U/天开始,以6例患者为一组逐步增加至4×10⁶ U/天。总体而言,局部给予IL-2耐受性良好。最常遇到的毒性反应是发热、肝毒性和低血压。在4×10⁶ U时出现剂量限制性毒性。在接受治疗的36例患者中,在2000 U和4×10⁶ U时观察到2例部分缓解。我们得出结论,局部给予IL-2在头颈部癌患者中耐受性良好,MTD为2×10⁶ U/天,与全身给予IL-2的报道相似。尽管总体缓解率较低,但延长IL-2给药时间或与其他生物制剂或细胞毒性药物联合使用可能会提高缓解率。

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