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SITC cancer immunotherapy resource document: a compass in the land of biomarker discovery

机译:SITC癌症免疫治疗资源文件:BIOMarker发现的指南针发现

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摘要

Since the publication of the Society for Immunotherapy of Cancer’s (SITC) original cancer immunotherapy biomarkers resource document, there have been remarkable breakthroughs in cancer immunotherapy, in particular the development and approval of immune checkpoint inhibitors, engineered cellular therapies, and tumor vaccines to unleash antitumor immune activity. The most notable feature of these breakthroughs is the achievement of durable clinical responses in some patients, enabling long-term survival. These durable responses have been noted in tumor types that were not previously considered immunotherapy-sensitive, suggesting that all patients with cancer may have the potential to benefit from immunotherapy. However, a persistent challenge in the field is the fact that only a minority of patients respond to immunotherapy, especially those therapies that rely on endogenous immune activation such as checkpoint inhibitors and vaccination due to the complex and heterogeneous immune escape mechanisms which can develop in each patient. Therefore, the development of robust biomarkers for each immunotherapy strategy, enabling rational patient selection and the design of precise combination therapies, is key for the continued success and improvement of immunotherapy. In this document, we summarize and update established biomarkers, guidelines, and regulatory considerations for clinical immune biomarker development, discuss well-known and novel technologies for biomarker discovery and validation, and provide tools and resources that can be used by the biomarker research community to facilitate the continued development of immuno-oncology and aid in the goal of durable responses in all patients.
机译:由于社会对癌症的(SITC)的免疫原的癌症免疫疗法的生物标志物的资源文件的发布,已经出现了在癌症免疫疗法显着的突破,特别是在发展和免疫检查点抑制剂的批准,工程细胞疗法,并释放出抗肿瘤肿瘤疫苗免疫活动。这些突破的最值得注意的特征是在一些患者中实现持久的临床反应,从而能够长期存活。这些耐用的反应已经注意到肿瘤类型未以前未被认为是免疫疗法敏感的,这表明所有癌症患者可能有可能受益免于免疫疗法。然而,该领域的持续挑战是,只有少数患者对免疫疗法作出反应,特别是那些依赖于内源性免疫活化的疗法,例如检查点抑制剂和疫苗接种,由于它们的复杂和异质的免疫逃逸机制,这病人。因此,为每种免疫疗法策略的鲁棒生物标志物的开发,实现理性患者选择和精确组合疗法的设计,是持续成功和免疫疗法的关键。在本文件中,我们总结和更新了临床免疫生物标志物发育的建立的生物标志物,准则和监管考虑,讨论了众所周知的生物标志物发现和验证技术,并提供了生物标志物研究界可以使用的工具和资源促进免疫肿瘤学的持续发展,并援助所有患者的持久反应。

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