Hallahan D E, Vokes E E, Rubin S J, O'Brien S, Samuels B, Vijaykumar S, Kufe D W, Phillips R, Weichselbaum R R
Department of Medicine, University of Chicago Pritzker School of Medicine, Chicago, Illinois 60637, USA.
Cancer J Sci Am. 1995 Sep-Oct;1(3):204-9.
Tumor necrosis factor-alpha enhances x-ray killing of human tumor cells in vitro and enhances tumor control when combined with radiation in animal tumor models. To determine the toxicity and maximal tolerated dose of tumor necrosis factor-alpha given daily during radiotherapy, we conducted a phase I dose-escalation study combining tumor necrosis factor-alpha and radiation.
Thirty-one patients, including 14 patients with locally advanced primary tumors and 17 patients with metastatic sites, were entered into this study. Recombinant human tumor necrosis factor-alpha was administered intravenously at doses ranging from 10 microg/m2 to 150 microg/m2 4 hours prior to each radiation therapy session, which was given on consecutive days for a minimum of 2 weeks. Radiation was prescribed to localized fields, with dose fractions ranging from 150 to 300 cGy/day for palliation or control of locally advanced tumors.
Major toxicity requiring withdrawal from the study was independent of tumor necrosis factor-alpha dose and occurred in seven patients. Symptoms included angina in two patients, and hypotension, respiratory distress, atrial fibrillation, allergic reaction, and progressive leukopenia in one patient each. A tumor necrosis factor-alpha dose of 150 microg/m2 was the maximum dose administered. No single dose-limiting toxicity was observed and a maximal tolerated dose could not be defined. There was no obvious increase in in-field toxicity. Response to treatment was assessed in 20 patients. Complete regression within the irradiated field was achieved in four patients, partial regression in four, and a minimal response in four. A trend toward a greater response rate at higher doses of tumor necrosis factor-alpha was observed.
The maximal tolerated dose of tumor necrosis factor-alpha when given with radiotherapy is at least 150 microg/m2 and a dose-limiting toxicity was not observed. Future studies will show whether responses to treatment are increased over those expected with radiation alone. Tumor localization of tumor necrosis factor-alpha by gene therapy combined with radiation therapy may eliminate the systemic toxicity we observed.
肿瘤坏死因子-α 在体外可增强 X 线对人肿瘤细胞的杀伤作用,并且在动物肿瘤模型中与放疗联合应用时可增强肿瘤控制效果。为确定放疗期间每日给予肿瘤坏死因子-α 的毒性及最大耐受剂量,我们开展了一项将肿瘤坏死因子-α 与放疗相结合的 I 期剂量递增研究。
31 例患者纳入本研究,其中 14 例为局部晚期原发性肿瘤患者,17 例为有转移灶的患者。在每次放疗前 4 小时静脉注射重组人肿瘤坏死因子-α,剂量范围为 10 μg/m² 至 150 μg/m²,放疗连续进行至少 2 周,每日 1 次。放疗针对局部区域,姑息治疗或控制局部晚期肿瘤时,每日分次剂量范围为 150 至 300 cGy。
7 例患者出现了导致退出研究的主要毒性反应,该毒性反应与肿瘤坏死因子-α 剂量无关。症状包括 2 例患者出现心绞痛,1 例患者分别出现低血压、呼吸窘迫、房颤、过敏反应和进行性白细胞减少。肿瘤坏死因子-α 的最大给药剂量为 150 μg/m²。未观察到单一剂量限制毒性,也无法确定最大耐受剂量。野内毒性无明显增加。对 20 例患者的治疗反应进行了评估。4 例患者在照射野内实现完全缓解,4 例部分缓解,4 例有轻微反应。观察到肿瘤坏死因子-α 剂量较高时反应率有升高趋势。
放疗时肿瘤坏死因子-α 的最大耐受剂量至少为 150 μg/m²,未观察到剂量限制毒性。未来研究将表明联合治疗的反应是否比单纯放疗预期的反应有所增加。通过基因治疗使肿瘤坏死因子-α 定位于肿瘤部位并联合放射治疗可能会消除我们所观察到的全身毒性。