Department of Medical Oncology, IRCCS Fondazione Istituto Nazionale Tumori (INT), 20133 Milan, Italy.
Department of Medical Oncology, IRCCS Fondazione Istituto Nazionale Tumori (INT), 20133 Milan, Italy.
Cancer Treat Rev. 2022 Nov;110:102455. doi: 10.1016/j.ctrv.2022.102455. Epub 2022 Aug 18.
In ultra-rare sarcomas (URS) the conduction of prospective, randomized trials is challenging. Data from retrospective observational studies (ROS) may represent the best evidence available. ROS implicit limitations led to poor acceptance by the scientific community and regulatory authorities. In this context, an expert panel from the Connective Tissue Oncology Society (CTOS), agreed on the need to establish a set of minimum requirements for conducting high-quality ROS on the activity of systemic therapies in URS.
Representatives from > 25 worldwide sarcoma reference centres met in November 2020 and identified a list of topics summarizing the main issues encountered in ROS on URS. An online survey on these topics was distributed to the panel; results were summarized by descriptive statistics and discussed during a second meeting (November 2021).
Topics identified by the panel included the use of ROS results as external control data, the criteria for contributing centers selection, modalities for ensuring a correct pathological diagnosis and radiologic assessment, consistency of surveillance policies across centers, study end-points, risk of data duplication, results publication. Based on the answers to the survey (55 of 62 invited experts) and discussion the panel agreed on 18 statements summarizing principles of recommended practice.
These recommendations will be disseminated by CTOS across the sarcoma community and incorporated in future ROS on URS, to maximize their quality and favor their use as control data when results from prospective studies are unavailable. These recommendations could help the optimal conduction of ROS also in other rare tumors.
在超罕见肉瘤(URS)中,开展前瞻性、随机试验具有挑战性。来自回顾性观察性研究(ROS)的数据可能代表了现有最佳证据。ROS 隐含的局限性导致其不受科学界和监管机构的认可。在此背景下,结缔组织肿瘤学会(CTOS)的一个专家小组一致认为,有必要为在 URS 中开展关于系统治疗活性的高质量 ROS 制定一套最低要求。
来自 25 个以上全球肉瘤参考中心的代表于 2020 年 11 月会面,确定了一份总结 ROS 在 URS 中遇到的主要问题的主题列表。针对这些主题进行了在线调查,并对调查结果进行了描述性统计,然后在第二次会议(2021 年 11 月)上进行了讨论。
专家组确定的主题包括将 ROS 结果用作外部对照数据、纳入中心选择标准、确保正确病理诊断和影像学评估的方式、各中心之间监测政策的一致性、研究终点、数据重复风险、结果发表。根据调查(邀请的 62 位专家中的 55 位)的回答和讨论,专家组就总结推荐实践原则的 18 条声明达成一致。
CTOS 将在肉瘤界传播这些建议,并将其纳入未来的 URS ROS 中,以最大限度地提高其质量,并在无法获得前瞻性研究结果时将其作为对照数据使用。这些建议有助于在其他罕见肿瘤中优化 ROS 的开展。