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Evaluation of Traditional Chinese Medicine Herbs in Oncology Clinical Trials

机译:肿瘤临床试验中中药草药评价

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摘要

Despite wide empirical use and demand for traditional Chinese medicine (TCM) herbs worldwide, high-quality clinical trials of TCM herbs in oncology are limited. We developed recommendations for rigorous clinical trials to evaluate their safety and efficacy for oncology patients. To accomplish this goal, the TCM & Cancer Research Committee of the Chinese Pharmaceutical Association convened a working group of oncologists, TCM experts, clinical researchers, biostatisticians, and industry/government representatives to develop principles and approaches for TCM cancer drug clinical trials. They identified 2 categories of herbal drugs based on therapeutic intent: survival improvement and symptom management. The working group also emphasized the need to adopt international standards when appropriate for TCM herbal drug approval and to develop methodology to standardize diagnostic criteria, treatment approaches, and outcome measures according to defining TCM characteristics. These recommendations aim to improve study design and methods to inform rigorous investigation of TCM herbs in patients with cancer.
机译:尽管对全球中药(TCM)草药有广泛的实证使用和需求,但肿瘤中医草药的高质量临床试验有限。我们为严格的临床试验制定了建议,以评估其对肿瘤患者的安全性和疗效。为了实现这一目标,中国药业协会的中医和癌症研究委员会召开了一组肿瘤学家,中医专家,临床研究人员,生物统计学家和行业/政府代表,为中医癌症药物临床试验制定原则和方法。他们确定了基于治疗​​意图的2类药物药物:存活改善和症状管理。工作组还强调需要在适用于中医药物批准时采用国际标准,并根据定义中医特征来制定标准化诊断标准,治疗方法和结果措施的方法。这些建议旨在改善研究设计和方法,以便为癌症患者进行严格调查TCM草药。

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