A retrospective study evaluating the effect of trastuzumab addition to carboplatin/paclitaxel on overall survival in patients with advanced-stage HER2/neu-overexpressing uterine serous carcinoma or carcinosarcoma.

IF 8.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMC Medicine Pub Date : 2025-02-21 DOI:10.1186/s12916-025-03916-3
Ting-Fang Lu, Lou Sun, Yu-Hsiang Shih, Yen-Fu Chen, Chun-Ting Fan, Shao-Jing Wang, Shih-Tien Hsu, Chih-Ku Liu, Sheau-Feng Hwang, Chien-Hsing Lu
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Abstract

Background: Uterine serous carcinoma and carcinosarcoma are aggressive forms of endometrial cancer with poor survival outcomes. Trastuzumab, a human epidermal growth factor receptor-2 (HER2)-directed monoclonal antibody, has demonstrated tumoricidal efficacy. However, clinical data regarding its efficacy in uterine serous carcinoma are limited, and there are no clinical data available for uterine carcinosarcoma. Therefore, this study aimed to ascertain the efficacy and safety of adding trastuzumab to carboplatin and paclitaxel as a frontline treatment for advanced-stage HER2-overexpressing uterine serous carcinoma and carcinosarcoma.

Methods: This retrospective study used deidentified data from electronic health records from the TriNetX Research Network. Participants were identified using International Classification of Diseases codes, and HER2 positivity was confirmed through immunohistochemistry or fluorescence in situ hybridisation. Propensity score matching was employed to reduce confounders, and survival outcomes and adverse events were assessed.

Results: Following propensity score matching, 280 patients with advanced HER2-positive uterine serous carcinoma or carcinosarcoma were analysed. The group of patients treated with carboplatin/paclitaxel + trastuzumab (CP + T) showed a significantly prolonged median overall survival compared to those treated exclusively with CP (41 months versus 25.2 months, hazard ratio [HR] = 0.51, p = 0.002) in both advanced-stage uterine carcinosarcoma and serous carcinoma. Specifically, patients with uterine carcinosarcoma experienced a prolonged survival benefit (HR = 0.39, p < 0.0001) when trastuzumab was added to their chemotherapy regimen, which surpassed the survival benefit observed in patients with uterine serous carcinoma (HR = 0.56, p = 0.04). However, patients who received trastuzumab experienced increased rates of hypertension, diarrhoea, and left ventricular systolic dysfunction.

Conclusions: The addition of trastuzumab to frontline chemotherapy is effective in treating HER2-overexpressing uterine serous carcinoma and carcinosarcoma, particularly uterine carcinosarcoma. However, careful monitoring of adverse cardiac events is needed.

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一项回顾性研究评估曲妥珠单抗联合卡铂/紫杉醇对晚期HER2/ new过表达子宫浆液性癌或癌肉瘤患者总生存期的影响。
背景:子宫浆液性癌和癌肉瘤是侵袭性子宫内膜癌,生存预后差。曲妥珠单抗是一种人表皮生长因子受体-2 (HER2)导向的单克隆抗体,已证明具有杀肿瘤功效。然而,其治疗子宫浆液性癌的临床资料有限,治疗子宫癌肉瘤尚无临床资料。因此,本研究旨在确定曲妥珠单抗联合卡铂和紫杉醇作为一线治疗晚期her2过表达子宫浆液性癌和癌肉瘤的有效性和安全性。方法:本回顾性研究使用来自TriNetX研究网络的电子健康记录的未识别数据。使用国际疾病分类代码对参与者进行鉴定,并通过免疫组织化学或荧光原位杂交证实HER2阳性。采用倾向评分匹配来减少混杂因素,并评估生存结果和不良事件。结果:采用倾向评分匹配法对280例晚期her2阳性子宫浆液癌或癌肉瘤患者进行了分析。在晚期子宫癌肉瘤和浆液性癌中,接受卡铂/紫杉醇+曲妥珠单抗(CP + T)治疗的患者比只接受CP治疗的患者(41个月vs 25.2个月,风险比[HR] = 0.51, p = 0.002)均显着延长了中位总生存期。结论:一线化疗加用曲妥珠单抗治疗her2过表达的子宫浆液性癌和癌肉瘤,尤其是宫癌肉瘤是有效的。然而,需要仔细监测心脏不良事件。
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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