Ledermann Jonathan A, Ray-Coquard Isabelle
From the UCL Cancer Institute, London, United Kingdom; Department of Adult Medical Oncology, Centre Leon Berard, Lyon, France.
Am Soc Clin Oncol Educ Book. 2014:e282-6. doi: 10.14694/EdBook_AM.2014.34.e282.
More than 50% of all gynecologic cancers can be classified as rare tumors (defined as an incidence of fewer than six per 100,000). Improved understanding of the molecular pathogenesis of tumors increases the proportion of rare tumors and creates challenges in optimizing the design of clinical trials. Novel trial designs are needed to take forward the development of new treatments in rare tumors. This requires international partnerships, harmonization of treatment, and collaboration to overcome the regulatory barriers to conducting international trials. Although randomized trials can be done in many tumor types, there are some for which conducting even single-arm studies may be challenging. For these tumors, robust collection of data through national and/or international registries could lead through audit to improvements in the treatment of rare tumors.
超过50%的妇科癌症可归类为罕见肿瘤(定义为每10万人中发病率低于6例)。对肿瘤分子发病机制的深入了解增加了罕见肿瘤的比例,并在优化临床试验设计方面带来了挑战。需要新的试验设计来推动罕见肿瘤新疗法的开发。这需要国际合作、治疗方法的协调统一以及协作,以克服开展国际试验的监管障碍。尽管随机试验可在多种肿瘤类型中进行,但有些肿瘤即使开展单臂研究也可能具有挑战性。对于这些肿瘤,通过国家和/或国际登记处有力地收集数据,经审核后可能会改善罕见肿瘤的治疗。