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病例报告:在一名接受过大量治疗的晚期雌激素受体阳性/人表皮生长因子受体2阴性且肿瘤突变负荷高的乳腺癌患者中,免疫检查点抑制剂卡瑞利珠单抗产生显著反应。

Case Report: Significant Response to Immune Checkpoint Inhibitor Camrelizumab in a Heavily Pretreated Advanced ER+/HER2- Breast Cancer Patient With High Tumor Mutational Burden.

作者信息

Wang Rong, Yang Yuchen, Ye Wei-Wu, Xiang Jianxing, Chen Songan, Zou Wei-Bin, Wang Xiao-Jia, Chen Tianhui, Cao Wen-Ming

机构信息

Department of Breast Medical Oncology, Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Hangzhou, China.

Institute of Cancer and Basic Medicine (IBMC), Chinese Academy of Sciences, Hangzhou, China.

出版信息

Front Oncol. 2021 Feb 9;10:588080. doi: 10.3389/fonc.2020.588080. eCollection 2020.

Abstract

Endocrine treatment plus CDK4/6 inhibitors have become standard of care for estrogen receptor positive (ER+) breast cancer. Although immune checkpoint inhibitors (ICIs) have shown promising antitumor activity in a variety of cancer types, only limited success has been achieved for metastatic breast cancer (mBC) patients, especially the ER+ subtype, which usually exhibit lower tumor mutation burden (TMB) compared with other subtypes and therefore perceived as immunologically quiescent. Here we present a case of an ER+/HER2- but TMB-high mBC patient who had significant response to combination therapy with anti-PD-1 antibody camrelizumab and vinorelbine and obtained partial response (PR) with a progression-free survival (PFS) of 5 months after failure of multiple lines of therapy. Our case indicates that TMB may serve as a potential biomarker in immunotherapy selection for normally immunologically "cold" tumors such as ER+ mBC, also molecular monitoring during the whole treatment course plays an important role in patient management.

摘要

内分泌治疗联合CDK4/6抑制剂已成为雌激素受体阳性(ER+)乳腺癌的标准治疗方案。尽管免疫检查点抑制剂(ICI)在多种癌症类型中已显示出有前景的抗肿瘤活性,但转移性乳腺癌(mBC)患者,尤其是ER+亚型患者,仅取得了有限的成功,该亚型通常与其他亚型相比肿瘤突变负荷(TMB)较低,因此被认为免疫原性较低。在此,我们报告一例ER+/HER2-但TMB高的mBC患者,该患者在多线治疗失败后,对抗PD-1抗体卡瑞利珠单抗和长春瑞滨联合治疗有显著反应,并获得部分缓解(PR),无进展生存期(PFS)为5个月。我们的病例表明,TMB可能作为免疫治疗选择的潜在生物标志物,用于如ER+ mBC等通常免疫原性“冷”的肿瘤,并且整个治疗过程中的分子监测在患者管理中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8122/7900143/23a6dc26c3d8/fonc-10-588080-g001.jpg

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