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巨大溃疡型局部晚期乳腺癌对低分割放疗联合阿帕替尼治疗有效:一例报告及文献综述

Giant Fungated Locally Advanced Breast Carcinoma Responded to Hypofractionated Radiotherapy Combined with Apatinib: A Case Report and Literature Review.

作者信息

Liu Hui, Liu Bailong, Ma Yunfei, Guo Liang, Wu Di, Shi Aiping, Liu Min

机构信息

Department of Radiation Oncology, The First Hospital of Jilin University, Changchun 130021, People's Republic of China.

Department of Pathology, The First Hospital of Jilin University, Changchun 130021, People's Republic of China.

出版信息

Cancer Manag Res. 2021 Jan 22;13:605-611. doi: 10.2147/CMAR.S291029. eCollection 2021.

Abstract

Locally advanced breast cancer (LABC) is frequently encountered in clinical practice. Primary systemic therapy is regarded as the cornerstone of LABC management to downstage the disease and enable surgery. However, multiple lines of systemic agents may fail to control tumor growth in a considerable number of patients, and few options remain available for such patients. Here, we present a case of triple-negative, right breast cancer that progressed aggressively despite 3 lines of standard chemotherapy. The patient suffered from severe skin ulceration, bleeding, pain, infection, and fungation. The small-molecular tyrosine kinase inhibitor (TKI) apatinib was initiated, which targets vascular endothelial growth factor receptor 2 (VEGFR2). The patient then underwent hypofractionated irradiation applied to the whole right breast at 40 Gy/8 f. The tumor responded dramatically to this combination, and a near-complete remission (CR) response was achieved 2 months after irradiation. Our case is novel and instructional and demonstrated the efficacy and safety of hypofractionated irradiation combined with antiangiogenesis for the treatment of intractable LABC, shedding light on this difficult situation. In the near future, large-scale clinical trials will be initiated to further explore this issue.

摘要

局部晚期乳腺癌(LABC)在临床实践中经常遇到。原发性全身治疗被视为LABC治疗的基石,以降低疾病分期并实现手术。然而,在相当数量的患者中,多线全身治疗药物可能无法控制肿瘤生长,对于这类患者几乎没有其他选择。在此,我们报告一例三阴性右乳腺癌患者,尽管接受了3线标准化疗,病情仍进展迅速。患者出现严重的皮肤溃疡、出血、疼痛、感染和溃烂。开始使用靶向血管内皮生长因子受体2(VEGFR2)的小分子酪氨酸激酶抑制剂(TKI)阿帕替尼。然后对患者右侧全乳进行40 Gy/8次的大分割放疗。肿瘤对这种联合治疗反应显著,放疗后2个月实现了近完全缓解(CR)。我们的病例新颖且具有指导意义,证明了大分割放疗联合抗血管生成治疗难治性LABC的有效性和安全性,为这一难题提供了思路。在不久的将来,将开展大规模临床试验以进一步探索这一问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/967e/7837545/d8cbcec7a00d/CMAR-13-605-g0001.jpg

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