伊瑞布林与卡培他滨联合治疗复发浸润性乳腺癌--一项单机构回顾性研究

Soumita Poddar, Amitabha Chakrabarti, Bodhisattwa Dutta, Santu Mondal, Rejakul Islam, Azizul Purkait
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引用次数: 0

摘要

背景:浸润性乳腺癌是目前最常见的癌症。由于这种疾病具有全身性,化疗在浸润性乳腺癌的治疗中发挥着重要作用。这种疾病的复发(局部区域性或转移性)并不少见。艾瑞布林和卡培他滨作为单药对复发疾病均有效。但这两种化疗药物联合使用的疗效尚不清楚。在这项单一机构的回顾性研究中,对复发乳腺癌患者进行了艾瑞布林和卡培他滨联合化疗的评估。材料和方法研究对象包括 ER 和/或 PR 阳性、Her-2/neu 阴性或三阴状态的复发性乳腺癌患者,他们在接受艾瑞布林治疗的同时还接受了卡培他滨治疗。本研究的首要目标是评估反应、无进展生存期(PFS)和总生存期(OS)。次要目标是毒性评估。研究结果研究共纳入 48 名患者。患者的中位年龄为 56 岁。36例(75%)患者ER和/或PR阳性,12例(25%)患者ER/PR阴性。5名(10.4%)患者获得了完全反应(CR)。32名(66.7%)患者获得部分应答(PR)。9名患者(18.8%)病情稳定(SD)。2名患者(4.2%)病情进展(PD)。中位无进展生存期(PFS)为 10.15 个月。患者的平均无进展生存期为 10.72 (95% CI- 9.72-11.72) 个月。中位总生存期(OS)为 18.15 个月。患者总生存期的平均值为 19.56 (95% CI- 17.9-21.22) 个月。分别有 19 名(39.6%)和 3 名(6.2%)患者出现 2 级和 3 级贫血。分别有 18 名(37.5%)和 2 名(4.2%)患者出现 2 级和 3 级中性粒细胞减少症。一名患者出现 2 级血小板减少症。19名患者(39.6%)出现二级腹泻。一名患者出现三级腹泻。8名患者(16.7%)出现跖红细胞增多症。六名患者(12.5%)出现二级神经病变。两名患者(4.2%)出现三级神经病变。19名患者(39.6%)出现了疲劳症状。结论伊瑞布林联合卡培他滨可用于曾使用过蒽环类和紫杉类药物的复发浸润性乳腺癌患者,其反应率和生存率均优于单药化疗。这种治疗方案对于化疗选择有限的三阴性乳腺癌(TNBC)尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eribulin along with capecitabine in relapsed invasive breast cancer- a retrospective single-Institutional study
Background: Invasive breast cancer is the most commonly diagnosed cancer at present. Due to systemic nature of disease, chemotherapy plays an important role in treatment of invasive breast cancer. Relapse (loco-regional or metastatic) is not uncommon in this disease. Both eribulin and capecitabine are effective as single agent in relapsed disease. But in combination, efficacy of these two chemotherapeutic medicines are not properly known. In this single-Institutional retrospective study, Eribulin and capecitabine have been assessed as combination chemotherapy in patients with relapsed breast cancer. Materials and methods: Patients with relapsed breast cancer, having ER and/or PR positive, Her-2/neu negative or triple negative status and received eribulin alongwith capecitabine, were included in our study. Primary objective of this study was to assess response, progression-free survival (PFS) and overall survival (OS). Secondary objective was toxicity assessment. Results: 48 patients were included in our study. Median age of patients was 56 years. Thirty six (75%) patients had ER and/or PR positive status and twelve (25%) patients had ER/PR negative status. Five (10.4%) patients achieved complete response (CR). Thirty two (66.7%) patients achieved partial response (PR). Disease was stable (SD) in nine (18.8%) patients. Two (4.2%) patients suffered from progressive disease (PD). Median Progression-free survival (PFS) was 10.15 months. Mean of PFS of patients was 10.72 (95% CI- 9.72-11.72) months. Median overall survival (OS) was 18.15 months. Mean of overall survival of patients was 19.56 (95% CI- 17.9-21.22) months. Nineteen (39.6%) and three (6.2%) patients experienced grade 2 and grade 3 anemia respectively. Eighteen (37.5%) and two (4.2%) patients suffered from grade 2 and grade 3 neutropenia respectively. One patients experienced grade 2 thrombocytopenia. Nineteen (39.6%) patients experienced grade 2 diarrhoea. One patients suffered from grade 3 diarrhoea. Palmo-plantor erythrodysesthesia had been experienced by eight (16.7%) patients. Six (12.5%) patients suffered from grade 2 neuropathy. Two (4.2%) patients experienced grade 3 neuropathy. Fatigue had been experienced by 19 (39.6%) patients. Conclusion: Eribulin alongwith capectabine can be used in patients with relapsed invasive breast cancer, in whom anthracycline and taxane have previously been used; with response rate and survival better than either single agent chemotherapy. This regimen is important particularly for triple negative breast cancer (TNBC), where option for chemotherapy is limited.
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