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具有BRCA1和BRCA2基因双杂合性的转移性乳腺癌对奥拉帕尼有反应:一例报告。

Metastatic breast cancer with double heterozygosity for the and genes responding to olaparib: A case report.

作者信息

Shao Bin, Di Lijun

机构信息

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Breast Oncology, Peking University Cancer Hospital and Institute, Beijing 100142, P.R. China.

出版信息

Oncol Lett. 2024 Apr 9;27(6):253. doi: 10.3892/ol.2024.14387. eCollection 2024 Jun.

DOI:10.3892/ol.2024.14387
PMID:38646498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11027096/
Abstract

Olaparib was the first poly ADP-ribose polymerase inhibitor approved for patients with cancer with mutations in either or in China. To the best of our knowledge, however, no study has described the efficacy of olaparib for patients with breast cancer with double mutations in and . The present case report describes a patient with breast cancer with deleterious germline mutations in both and . The 56-year-old patient with multiple metastatic breast cancer underwent breast cancer resection with 12 years interval between removal of the left and right breast. Germline mutations in both (S405X) and (W2990X) were identified by NGS. She received two cycles of chemotherapy with a combination of albumin-bound paclitaxel and capecitabine; the response was progressive disease. Subsequently, the patient was treated with a gradual dosage of decreasing olaparib (600 to 300 mg BID) for 6 months until grade 3 anemia could not be alleviated by giving erythropoietin and iron, and CT imaging showed a partial response (35% reduction). The patient then switched to exemestane therapy due to the continuous grade 3 anemia. In conclusion, the present study reported a female patient with double heterozygosity of BRCA1 and BRCA2 who benefited from olaparib monotherapy. Thus, olaparib may be a suitable treatment for such patients.

摘要

奥拉帕利是中国首个获批用于治疗携带BRCA1或BRCA2突变癌症患者的聚腺苷二磷酸核糖聚合酶抑制剂。然而,据我们所知,尚无研究描述奥拉帕利对携带BRCA1和BRCA2双突变乳腺癌患者的疗效。本病例报告描述了一名携带BRCA1和BRCA2有害胚系双突变的乳腺癌患者。这位56岁的多发转移性乳腺癌患者接受了乳腺癌切除术,左右乳房切除间隔12年。通过二代测序(NGS)鉴定出BRCA1(S405X)和BRCA2(W2990X)的胚系突变。她接受了两个周期的白蛋白结合型紫杉醇和卡培他滨联合化疗,疗效为疾病进展。随后,患者接受逐渐减量的奥拉帕利(600至300mg,每日两次)治疗6个月,直至给予促红细胞生成素和铁剂后3级贫血仍无法缓解,且CT成像显示部分缓解(缩小35%)。由于持续的3级贫血,患者随后改用依西美坦治疗。总之,本研究报告了一名BRCA1和BRCA2双杂合性的女性患者,其从奥拉帕利单药治疗中获益。因此,奥拉帕利可能是这类患者的合适治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/11e965768689/ol-27-06-14387-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/b0ff3b4ac787/ol-27-06-14387-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/70241bcbf967/ol-27-06-14387-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/11e965768689/ol-27-06-14387-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/b0ff3b4ac787/ol-27-06-14387-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/70241bcbf967/ol-27-06-14387-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3670/11027096/11e965768689/ol-27-06-14387-g02.jpg

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本文引用的文献

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Chinese Society of Clinical Oncology (CSCO) Breast Cancer Guidelines 2022.中国临床肿瘤学会(CSCO)乳腺癌诊疗指南2022
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A meta-analysis of reversion mutations in BRCA genes identifies signatures of DNA end-joining repair mechanisms driving therapy resistance.一项关于 BRCA 基因回复突变的荟萃分析确定了驱动治疗耐药性的 DNA 末端连接修复机制的特征。
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