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放射治疗肿瘤学组关于米索硝唑的临床试验。

Radiation Therapy Oncology Group clinical trials with misonidazole.

作者信息

Wasserman T H, Stetz J, Phillips T L

出版信息

Cancer. 1981 May 15;47(10):2382-90. doi: 10.1002/1097-0142(19810515)47:10<2382::aid-cncr2820471010>3.0.co;2-f.

Abstract

This paper presents a review of the progressive clinical trials of the hypoxic cell radiosensitizer, misonidazole, in the Radiation Therapy Oncology Group (RTOG). Presentation is made of all the schemas of the recently completed and currently active RTOG Phase II and Phase III studies. Detailed information is provided on the clinical toxicity of the Phase II trials, specifically regarding neurotoxicity. With limitations in drug total dose, a variety of dose schedules have proven to be tolerable, with a moderate incidence of nausea and vomiting and mild peripheral neuropathy, and a low incidence of more severe peripheral neuropathy or central neuropathy. No other organ toxicity has been seen, specifically no liver, renal or bone marrow toxicities. The clinical pharmacologic monitoring of misonidazole blood levels has been satisfactory with good correlation between the group-wide (Phase II) UV values and the HPLC values from the Phase I study. The patient accrual of the trials has been rapidly increasing and an early analysis suggests efficacy better than previous radiation experience. A series of eight Phase III trials are currently underway or proposed in the RTOG and the results of these are pending. An additional Phase III malignant glioma trial in the Brain tumor Study Group is described.

摘要

本文综述了放射治疗肿瘤学组(RTOG)中乏氧细胞放射增敏剂米索硝唑的进展性临床试验。介绍了RTOG近期完成的和目前正在进行的II期和III期研究的所有方案。提供了关于II期试验临床毒性的详细信息,特别是关于神经毒性的信息。在药物总剂量有限的情况下,已证明多种给药方案是可耐受的,恶心和呕吐的发生率中等,外周神经病变较轻,更严重的外周神经病变或中枢神经病变的发生率较低。未观察到其他器官毒性,特别是没有肝脏、肾脏或骨髓毒性。米索硝唑血药浓度的临床药理监测结果令人满意,全组(II期)紫外线值与I期研究的高效液相色谱值之间具有良好的相关性。试验的患者入组人数一直在迅速增加,早期分析表明疗效优于以往的放疗经验。RTOG目前正在进行或计划进行一系列八项III期试验,其结果尚待确定。还描述了脑肿瘤研究组中一项额外的III期恶性胶质瘤试验。

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