JSCO—ESMO—ASCO—JSMO—TOS: international expert consensus recommendations for tumour-agnostic treatments in patients with solid tumours with microsatellite instability or NTRK fusions

医学 彭布罗利珠单抗 微卫星不稳定性 肿瘤科 临床试验 伴生诊断 内科学 临床肿瘤学 trk受体 癌症 免疫疗法 受体 神经营养素 基因 微卫星 等位基因 生物化学 化学
作者
Takayuki Yoshino,G. Pentheroudakis,Saori Mishima,Michael J. Overman,Kun‐Huei Yeh,Eishi Baba,Yoichi Naito,Felipe A. Calvo,Ajit Kumar Saxena,L.-T. Chen,Masayuki Takeda,Andrés Cervantes,Hiroya Taniguchi,Kazuhiro Yoshida,Yasuhiro Kodera,Yuko Kitagawa,Josep Tabernero,Howard A. Burris,J.-Y. Douillard
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:31 (7): 861-872 被引量:112
标识
DOI:10.1016/j.annonc.2020.03.299
摘要

A Japan Society of Clinical Oncology (JSCO)-hosted expert meeting was held in Japan on 27 October 2019, which comprised experts from the JSCO, the Japanese Society of Medical Oncology (JSMO), the European Society for Medical Oncology (ESMO), the American Society of Clinical Oncology (ASCO), and the Taiwan Oncology Society (TOS). The purpose of the meeting was to focus on what we have learnt from both microsatellite instability (MSI)/deficient mismatch repair (dMMR) biomarkers in predicting the efficacy of anti-programmed death-1 (PD-1)/programmed death ligand-1 (PD-L1) immunotherapy, and the neurotrophic tyrosine receptor kinase (NTRK) gene fusions in predicting the efficacy of inhibitors of the tropomyosin receptor kinase (TRK) proteins across a range of solid tumour types. The recent regulatory approvals of the anti-PD-1 antibody pembrolizumab and the TRK inhibitors larotrectinib and entrectinib, based on specific tumour biomarkers rather than specific tumour type, have heralded a paradigm shift in cancer treatment approaches. The purpose of the meeting was to develop international expert consensus recommendations on the use of such tumour-agnostic treatments in patients with solid tumours. The aim was to generate a reference document for clinical practice, for pharmaceutical companies in the design of clinical trials, for ethics committees in the approval of clinical trial protocols and for regulatory authorities in relation to drug approvals, with a particular emphasis on diagnostic testing and patient selection.

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