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一个观点:将 ctDNA 纳入实体瘤反应评估标准 1.1 用于 II 期免疫治疗临床试验。

A perspective: the integration of ctDNA into Response Evaluation Criteria in Solid Tumours 1.1 for phase II immunotherapy clinical trials.

机构信息

School of Medicine, Department of Medical Oncology, Gaziantep University, Gaziantep, 27310, Turkey.

Department of Medical Oncology, Istinye University Topkapı Health Sciences Campus, Istanbul, 34295, Turkey.

出版信息

Immunotherapy. 2024 Mar;16(5):319-329. doi: 10.2217/imt-2023-0184. Epub 2024 Jan 10.

Abstract

A consensus guideline, iRECIST, was developed by the Response Evaluation Criteria in Solid Tumours (RECIST) working group for the use of the modified RECIST version 1.1 in cancer immunotherapy trials. iRECIST was designed to separate pseudoprogression from real progression. However, this is not the only ambiguous situation. In clinical immunotherapy trials, stable disease may reflect three tumor responses, including real stable disease, progressive disease and responsive disease. The prediction of a " is also important. Much data has accumulated showing that ctDNA can guide decisions at this point; thus, integrating ctDNA into the RECIST 1.1 criteria may help to distinguish a true tumor response type earlier in patients treated with immunotherapy; however, prospectively designed validation studies are needed.

摘要

免疫治疗相关实体瘤疗效评价标准 iRECIST 的开发:为了在癌症免疫治疗试验中使用改良版 RECIST 1.1 版,实体瘤反应评价标准(RECIST)工作组制定了共识指南 iRECIST。iRECIST 的设计目的是区分假性进展和真性进展。然而,这并不是唯一存在模糊情况的地方。在临床免疫治疗试验中,稳定疾病可能反映了三种肿瘤反应,包括真正的稳定疾病、进展性疾病和有反应性疾病。预测“假性进展”也很重要。大量数据表明,ctDNA 可以在此提供指导;因此,将 ctDNA 纳入 RECIST 1.1 标准可能有助于在接受免疫治疗的患者中更早地区分真正的肿瘤反应类型;然而,需要进行前瞻性设计的验证研究。

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