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与卡铂联合紫杉醇相比,仑伐替尼联合帕博利珠单抗用于经卡铂和紫杉醇治疗过的复发性或晚期子宫内膜癌。

Lenvatinib plus pembrolizumab compared to carboplatin plus paclitaxel for carboplatin and paclitaxel pretreated, recurrent, or advanced endometrial cancer.

作者信息

Wang Shao-Jing, Sun Lou, Shih Yu-Hsiang, Lu Ting-Fang, Chen Yen-Fu, Hsu Shih-Tien, Liu Chin-Ku, Hwang Sheau-Feng, Chen Jem-Kun, Chen Hsin-Hua, Lu Chien-Hsing

机构信息

Department of Obstetrics and Gynecology, Taichung Veterans General Hospital, 1650 Taiwan Boulevard Sect. 4, Taichung, ROC, 40705, Taiwan.

Department of Food and Nutrition, Providence University, Taichung, Taiwan.

出版信息

BMC Med. 2025 Mar 14;23(1):160. doi: 10.1186/s12916-025-03989-0.

Abstract

BACKGROUND

Lenvatinib plus pembrolizumab has demonstrated improved survival compared with doxorubicin or paclitaxel monotherapy in patients with advanced or recurrent endometrial cancers (ECs). However, response rates to monotherapy are poor in recurrent settings. Herein, we performed a retrospective analysis using real-world data to compare the outcomes of lenvatinib plus pembrolizumab, carboplatin plus paclitaxel (PT), and doxorubicin for patients with PT-pretreated, advanced, or recurrent ECs.

METHODS

We performed a multi-institutional retrospective analysis using de-identified electronic health record database (TriNetX) to compare lenvatinib plus pembrolizumab, carboplatin plus paclitaxel (PT), and doxorubicin outcomes in patients with PT-pretreated, advanced, or recurrent ECs. A 1:1 propensity score matching (PSM) was conducted. The primary outcome was the overall survival (OS) among treatment groups. The secondary outcome was the adverse event profile.

RESULTS

Between January 2012 and September 2023, we identified 397 patients with PT-treated, advanced, or recurrent ECs who received lenvatinib plus pembrolizumab, and 469 patients receiving PT at a platinum-free interval of over 6 months. Following PSM, no significant difference in median OS was observed between the lenvatinib plus pembrolizumab and re-challenge PT groups (19.1 vs. 18.5 months, p = 0.60; hazard ratio: 1.08, 95% confidence interval 0.81-1.46). However, lenvatinib plus pembrolizumab provided better survival benefits than doxorubicin. Adverse event analysis showed more hypothyroidism, hypertension, and proteinuria with lenvatinib plus pembrolizumab, and more hematologic toxicities in both chemotherapy groups.

CONCLUSIONS

Lenvatinib plus pembrolizumab was not associated with improved survival when compared with re-challenge PT in patients with a platinum-free interval of over 6 months. Re-challenge PT remains a valid option for PT-treated, recurrent, or advanced ECs, especially in patients with a substantially long platinum-free interval.

摘要

背景

在晚期或复发性子宫内膜癌(EC)患者中,与阿霉素或紫杉醇单药治疗相比,乐伐替尼联合帕博利珠单抗已显示出更长的生存期。然而,在复发情况下,单药治疗的缓解率较低。在此,我们使用真实世界数据进行了一项回顾性分析,以比较乐伐替尼联合帕博利珠单抗、卡铂联合紫杉醇(PT)和阿霉素治疗既往接受过PT治疗的晚期或复发性EC患者的疗效。

方法

我们使用去识别化的电子健康记录数据库(TriNetX)进行了一项多机构回顾性分析,以比较乐伐替尼联合帕博利珠单抗、卡铂联合紫杉醇(PT)和阿霉素治疗既往接受过PT治疗的晚期或复发性EC患者的疗效。进行了1:1倾向评分匹配(PSM)。主要结局是各治疗组的总生存期(OS)。次要结局是不良事件谱。

结果

在2012年1月至2023年9月期间,我们确定了397例接受过PT治疗的晚期或复发性EC患者接受了乐伐替尼联合帕博利珠单抗治疗,469例患者在无铂间期超过6个月时接受了PT治疗。PSM后,乐伐替尼联合帕博利珠单抗组和再次挑战PT组的中位OS无显著差异(19.1个月对18.5个月,p = 0.60;风险比:1.08,95%置信区间0.81 - 1.46)。然而,乐伐替尼联合帕博利珠单抗比阿霉素提供了更好的生存获益。不良事件分析显示,乐伐替尼联合帕博利珠单抗组甲状腺功能减退、高血压和蛋白尿更多,两个化疗组血液学毒性更多。

结论

在无铂间期超过6个月的患者中,与再次挑战PT相比,乐伐替尼联合帕博利珠单抗并未改善生存期。再次挑战PT仍然是既往接受过PT治疗的复发性或晚期EC患者的有效选择,特别是在无铂间期相当长的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f196/11909920/d3134e6f49f8/12916_2025_3989_Fig1_HTML.jpg

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