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TIP25-243: Randomized Study Evaluating Optimal Dose, Efficacy and Safety of E7386 + Lenvatinib Versus Treatment of Physicians' Choice in Advance/Recurrent Endometrial Carcinoma Previously Treated With Anti-PD-(L)1 Immunotherapy.

作者信息

Eskander Ramez, Lee Jung-Yun, Mirza Mansoor, Lorusso Domenica, Mackay Helen, Ray-Coquard Isabelle, Oaknin Ana, Gonzalez-Martin Antonio, Hasegawa Kosei, Corr Bradley, Wu Xiaohua, Leary Alexandra, Hu Tianle, Dutta Lea, Okpara Chinyere, McKenzie Jodi, Makker Vicky

机构信息

1Division of Gynecologic Oncology, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Diego, Moores Cancer Center, La Jolla, CA.

2Yonsei Cancer Center and Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.

出版信息

J Natl Compr Canc Netw. 2025 Mar 28;23(3.5):TIP25-243. doi: 10.6004/jnccn.2024.7252.

DOI:10.6004/jnccn.2024.7252
PMID:40157347
Abstract
摘要

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TIP25-243: Randomized Study Evaluating Optimal Dose, Efficacy and Safety of E7386 + Lenvatinib Versus Treatment of Physicians' Choice in Advance/Recurrent Endometrial Carcinoma Previously Treated With Anti-PD-(L)1 Immunotherapy.
J Natl Compr Canc Netw. 2025 Mar 28;23(3.5):TIP25-243. doi: 10.6004/jnccn.2024.7252.
2
Randomized study evaluating optimal dose, efficacy, and safety of E7386 plus lenvatinib versus treatment of physician's choice in advanced/recurrent endometrial carcinoma previously treated with platinum-based chemotherapy and immune checkpoint inhibitors.一项随机研究,评估E7386联合乐伐替尼的最佳剂量、疗效和安全性,对比在先前接受铂类化疗和免疫检查点抑制剂治疗的晚期/复发性子宫内膜癌中医生选择的治疗方案。
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Lenvatinib plus pembrolizumab in patients with advanced endometrial cancer: an interim analysis of a multicentre, open-label, single-arm, phase 2 trial.仑伐替尼联合帕博利珠单抗治疗晚期子宫内膜癌患者:一项多中心、开放标签、单臂、2 期临床试验的中期分析。
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引用本文的文献

1
Clinical outcome of advanced or recurrent endometrial carcinoma treated with chemotherapy: a French observational retrospective cohort: the ENDOVIE study.化疗治疗晚期或复发性子宫内膜癌的临床结局:一项法国观察性回顾性队列研究:ENDOVIE研究
BMJ Open. 2025 Sep 4;15(9):e096837. doi: 10.1136/bmjopen-2024-096837.