A Retrospective Real-World Study of Pyrotinib in HER-2 Positive Advanced Breast Cancer.

IF 2.6 4区 医学 Q3 ONCOLOGY Cancer Management and Research Pub Date : 2025-03-04 eCollection Date: 2025-01-01 DOI:10.2147/CMAR.S486211
Zhi Yang, Wei-Da Fu, Hua-Yan Gu, Jia-Ling Ding, Gui-Long Guo
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Abstract

Purpose: To explore the efficacy and safety of pyrotinib in a real-world setting in a population with HER2-positive advanced breast cancer, subgroup analysis was conducted based on different clinicopathological features to further explore the general characteristics of patients, tumor nature, and the effect of various lines of treatment before patients started pyrotinib on the efficacy of pyrotinib in the real-world study.

Methods: The clinical pathological characteristics, drug efficacy and related adverse reactions of HER2-positive MBC patients treated with pyrotinib in six hospitals in Southeast Zhejiang Province from February 2018 to December 2023 were collected and analyzed retrospectively.

Results: A total of 342 patients with HER2-positive MBC were enrolled. The median follow-up time of 42.0 months. The median age of the overall population was 52 years (range from 25-90 year old). Median progression-free survival in the total population was 10.0 months, the median overall survival was 29.0 months. The (objective response rate, ORR) was 40.35% and the (disease control rate, DCR) was 83.92%. The median progression-free survival (PFS) in the total population was 10.0 months, the median overall survival was 29.0 months. And pyrotinib had better mPFS for advanced first-line treatment than for second-third-line and beyond(14.0 months vs.10.0 months vs.6.0 months, P<0.001). Multivariate Cox regression analysis showed that ECOG, HER2 status, brain metastasis, liver metastasis, number of pyrotinib treatment lines, previous lapatinib treatment, combined capecitabine therapy and trastuzumab resistance were independent prognostic factors for PFS. Diarrhea was the most common adverse reaction (ADR) in 205 patients (59.94%), which could be controlled by antidiarrheal drugs.

Conclusion: This multicenter study suggested that the use of pyrotinib for HER2 positive MBC had a relatively good efficacy, especially for those who received first-line pyrotinib treatment and those who were sensitive to previous trastuzumab treatment. Patients with brain metastasis and liver metastases also benefit from pyrotinib treatment, especially for patients treated with brain radiotherapy and/or surgery. ECOG, HER2 status, brain metastasis, liver metastasis, number of pyrotinib treatment lines, previous lapatinib treatment, combined capecitabine therapy and trastuzumab resistance were independent prognostic factors for PFS in HER2 Positive MBC patients treated with pyrotinib. The most common adverse reaction associated with pyrotinib is diarrhea, which can be well controlled through antidiarrheal treatment. Pyrotinib combined with vinorelbine has similar efficacy to pyrotinib combined with capecitabine and has fewer side effects, and can be used as an alternative to capecitabine.

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吡罗替尼治疗HER-2阳性晚期乳腺癌的回顾性现实世界研究。
目的:探讨吡罗替尼在现实世界中对her2阳性晚期乳腺癌患者的疗效和安全性,根据不同的临床病理特征进行亚组分析,进一步探讨患者的一般特征、肿瘤性质以及患者开始使用吡罗替尼前各种治疗方案对实际研究中吡罗替尼疗效的影响。方法:回顾性分析2018年2月至2023年12月浙江东南部6家医院her2阳性MBC患者使用吡罗替尼治疗的临床病理特点、疗效及相关不良反应。结果:共有342例her2阳性MBC患者入组。中位随访时间42.0个月。总体人口的年龄中位数为52岁(25-90岁)。中位无进展生存期为10.0个月,中位总生存期为29.0个月。客观缓解率ORR为40.35%,疾病控制率DCR为83.92%。中位无进展生存期(PFS)为10.0个月,中位总生存期为29.0个月。pyrotinib在晚期一线治疗的mPFS优于二三线及以上治疗的mPFS(14.0个月vs.10.0个月vs.6.0个月)。结论:本多中心研究提示,使用pyrotinib治疗HER2阳性MBC具有相对较好的疗效,特别是对于接受过一线pyrotinib治疗的患者和既往曲妥珠单抗治疗敏感的患者。脑转移和肝转移患者也受益于吡罗替尼治疗,特别是接受脑放疗和/或手术治疗的患者。ECOG、HER2状态、脑转移、肝转移、吡罗替尼治疗线数、既往拉帕替尼治疗、卡培他滨联合治疗和曲妥珠单抗耐药是吡罗替尼治疗HER2阳性MBC患者PFS的独立预后因素。吡罗替尼最常见的不良反应是腹泻,通过止泻治疗可以很好地控制腹泻。吡罗替尼联合长春瑞滨的疗效与吡罗替尼联合卡培他滨相似,且副作用更少,可作为卡培他滨的替代用药。
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来源期刊
Cancer Management and Research
Cancer Management and Research Medicine-Oncology
CiteScore
7.40
自引率
0.00%
发文量
448
审稿时长
16 weeks
期刊介绍: Cancer Management and Research is an international, peer reviewed, open access journal focusing on cancer research and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for cancer patients. Specific topics covered in the journal include: ◦Epidemiology, detection and screening ◦Cellular research and biomarkers ◦Identification of biotargets and agents with novel mechanisms of action ◦Optimal clinical use of existing anticancer agents, including combination therapies ◦Radiation and surgery ◦Palliative care ◦Patient adherence, quality of life, satisfaction The journal welcomes submitted papers covering original research, basic science, clinical & epidemiological studies, reviews & evaluations, guidelines, expert opinion and commentary, and case series that shed novel insights on a disease or disease subtype.
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