Selby P, Hobbs S, Viner C, Jackson E, Jones A, Newell D, Calvert A H, McElwain T, Fearon K, Humphreys J
Institute of Cancer Research, Royal Marsden Hospital, Sutton, Surrey, UK.
Br J Cancer. 1987 Dec;56(6):803-8. doi: 10.1038/bjc.1987.294.
Eighteen patients with advanced cancer have been treated intravenously with human recombinant tumour necrosis factor (rhTNF). The drug produced febrile reactions at all doses although these were preventable by steroids and indomethacin. Doses at or above 9 x 10(5) units (400 micrograms)m-2 were associated with hypotension, abnormal liver enzymes, leucopenia and mild renal impairment in a substantial proportion of patients. RhTNF was cleared from plasma with a half life of approximately 20 minutes but non-linear pharmacokinetics lymphoma, improvements in their tumours were recorded. RhTNF was noted to produce rapid increases in serum C-reactive protein concentrations. Endogenous TNF levels were not found to be elevated in 72 cancer patients. TNF deserves further therapeutic evaluation and these observations support its biological importance as an endogenous pyrogen, mediator of acute phase protein responses, and a mediator of endotoxic shock.
18例晚期癌症患者接受了静脉注射人重组肿瘤坏死因子(rhTNF)治疗。该药物在所有剂量下均会引起发热反应,不过可通过类固醇和吲哚美辛预防。在相当一部分患者中,剂量达到或高于9×10⁵单位(400微克)/m²会伴有低血压、肝酶异常、白细胞减少和轻度肾功能损害。rhTNF从血浆中清除,半衰期约为20分钟,但药代动力学呈非线性。在淋巴瘤患者中,记录到肿瘤有所改善。rhTNF可使血清C反应蛋白浓度迅速升高。在72例癌症患者中未发现内源性TNF水平升高。TNF值得进一步进行治疗评估,这些观察结果支持其作为内源性致热原、急性期蛋白反应介质和内毒素休克介质的生物学重要性。