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厄洛替尼对罕见表皮生长因子受体(EGFR)突变的乳腺癌疗效显著——病例报告

Excellent response to erlotinib in breast carcinoma with rare EGFR mutation-a case report.

作者信息

Singh Gunjesh Kumar, Bajpai Jyoti, Joshi Shalaka, Prabhash Kumar, Choughule Anuradha, Patil Asawari, Gupta Sudeep, Badwe Rajendra Achyut

机构信息

Department of Medical Oncology, Tata Memorial Hospital, Mumbai 400012, India.

Department of Surgical Oncology, Tata Memorial Hospital, Mumbai 400012, India.

出版信息

Ecancermedicalscience. 2020 Aug 25;14:1092. doi: 10.3332/ecancer.2020.1092. eCollection 2020.

Abstract

Triple negative breast carcinoma is a problematic subtype with poor outcomes. Many clinical trials are underway to find possible target to increase treatment options. Epidermal growth factor receptor (EGFR) has emerged as one such molecule which is over expressed in some of these patients and can be targeted by tyrosine kinase inhibitors. We describe a diagnostically challenging case of metastatic breast carcinoma, with extensive lung disease and poor Eastern Cooperative Oncology Group (ECOG) performance status, which expressed an uncommon EGFR mutation (Exon 21L861Q) and which benefitted from erlotinib following failure of all primary treatment modalities. The case uncovers the presence of these unusual mutations in breast carcinoma and highlights the importance of performing molecular analysis and the appropriate targeted therapy. This approach can be an important problem-solving tool, especially in cases where the patient is not fit for the other standard treatment options.

摘要

三阴性乳腺癌是一种预后较差的棘手亚型。目前正在进行许多临床试验,以寻找可能的靶点来增加治疗选择。表皮生长因子受体(EGFR)已成为这样一种分子,它在其中一些患者中过度表达,并且可以被酪氨酸激酶抑制剂靶向。我们描述了一例具有诊断挑战性的转移性乳腺癌病例,该患者有广泛的肺部疾病且东部肿瘤协作组(ECOG)体能状态较差,其表达了一种罕见的EGFR突变(外显子21 L861Q),并且在所有一线治疗方案失败后从厄洛替尼治疗中获益。该病例揭示了乳腺癌中这些不寻常突变的存在,并强调了进行分子分析和适当靶向治疗的重要性。这种方法可以成为一个重要的解决问题的工具,尤其是在患者不适合其他标准治疗选择的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722b/7498275/ec82619a5f5b/can-14-1092fig1.jpg

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