Expert consensus on the clinical application of immunotherapy in breast cancer: 2024.

Kun Wang, Jin Yang, Biyun Wang, Qiang Liu, Xiaojia Wang, Yongmei Yin, Haibo Wang, Shusen Wang, Chunfang Hao, Xiaopeng Hao, Yueping Liu, Zefei Jiang
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Abstract

Background: Significant progress has been made in immunotherapy of breast cancer (BC) with the approval of multiple immune checkpoint inhibitors (ICIs), particularly in early and metastatic triple-negative breast cancer (TNBC) settings. Most guidelines have recommended immune therapy as the important approach in BC, yet several critical aspects still require further clarification, including proper patient selection, treatment duration, optimized chemotherapy partner, predictive biomarkers, and specific considerations for Chinese patients.

Methods: (I) Establishment of expert group: the expert group consists of 32 experts from departments such as medical oncology, breast surgery, and pathology; (II) literature search: mainly conducted in English databases (such as PubMed, Embase, and Cochrane Library) and Chinese databases (such as China National Knowledge Infrastructure, China Biology Medicine disc, and Wanfang Database), with a search cutoff date of April 23, 2024; (III) assessment of evidence quality and recommendation strength: evidence quality and recommendation opinions are graded based on the evidence category and recommendation level of the Chinese Society of Clinical Oncology (CSCO) guidelines; (IV) consensus formulation: on the March 2, 2024, through online consensus meeting, the consensus content is thoroughly discussed, and opinions from all experts are solicited.

Results: The consensus meeting has resulted in 15 detailed recommendations, providing clearer guidance on the clinical application of immunotherapy in BC management. The core suggestions are as follows: for early-stage II-III TNBC and metastatic TNBC (mTNBC) in the first-line setting, programmed cell death protein 1 (PD-1) inhibitors can be considered. However, for hormone receptor-positive/human epidermal growth factor receptor 2-negative BC (HR+/HER2- BC), HER2+ BC, and mTNBC in later lines of therapy, evidence is lacking to support the use of immunotherapy.

Conclusions: This consensus provides a comprehensive overview of BC immunotherapy, including immunotherapy for early-stage BC and late-stage BC, immune related adverse event (irAE) management, biomarkers of immunotherapy, and future directions. The consensus consolidates these deliberations into 15 evidence-based recommendations, serving as a practical guide for clinicians to more scientifically and systematically manage the clinical application of immunotherapy.

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乳腺癌免疫疗法临床应用专家共识:2024 年。
背景:随着多种免疫检查点抑制剂(ICIs)的获批,乳腺癌(BC)的免疫治疗取得了重大进展,尤其是在早期和转移性三阴性乳腺癌(TNBC)中。大多数指南都建议将免疫疗法作为治疗乳腺癌的重要方法,但仍有几个关键方面需要进一步明确,包括患者的合理选择、治疗时间、优化化疗方案、预测性生物标志物以及中国患者的具体注意事项。方法:(I)成立专家组:专家组由来自肿瘤内科、乳腺外科、病理科等科室的32位专家组成;(II)文献检索:主要在英文数据库(如PubMed、Embase和Cochrane图书馆)和中文数据库(如中国知网、中国生物医学大辞典和万方数据库)中进行检索,检索截止日期为2024年4月23日;(III)证据质量和推荐强度评估:根据中国临床肿瘤学会(CSCO)指南的证据类别和推荐级别,对证据质量和推荐意见进行分级;(IV)形成共识:2024年3月2日,通过在线共识会议,对共识内容进行充分讨论,并征求所有专家的意见。结果:共识会议形成了 15 条详细建议,为免疫疗法在 BC 管理中的临床应用提供了更明确的指导。核心建议如下:对于早期II-III期TNBC和转移性TNBC(mTNBC)的一线治疗,可考虑使用程序性细胞死亡蛋白1(PD-1)抑制剂。然而,对于激素受体阳性/人表皮生长因子受体2阴性的BC(HR+/HER2- BC)、HER2+ BC和后期治疗的mTNBC,目前还缺乏支持使用免疫疗法的证据:本共识全面概述了BC免疫疗法,包括早期BC和晚期BC的免疫疗法、免疫相关不良事件(irAE)管理、免疫疗法的生物标志物以及未来发展方向。该共识将这些讨论整合为 15 项循证建议,为临床医生更科学、更系统地管理免疫疗法的临床应用提供了实用指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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