卡巴他赛和177Lu-PSMA-617在转移性去雄抵抗性前列腺癌中的比较:一项回顾性多中心研究(LuCaS)。

IF 7.6 1区 医学 Q1 ONCOLOGY
Hatice Bolek, Satı Coskun Yazgan, Furkan Ceylan, Jorge Esteban-Villarrubia, Cagatay Arslan, Tülay Kuş, Deniz Tural, Mehmet Ali Nahit Sendur, Nuriye Ozlem Kucuk, Elif Çıngı Özdemir, Elena Castro, Emre Yekedüz, Yüksel Ürün
{"title":"卡巴他赛和177Lu-PSMA-617在转移性去雄抵抗性前列腺癌中的比较:一项回顾性多中心研究(LuCaS)。","authors":"Hatice Bolek, Satı Coskun Yazgan, Furkan Ceylan, Jorge Esteban-Villarrubia, Cagatay Arslan, Tülay Kuş, Deniz Tural, Mehmet Ali Nahit Sendur, Nuriye Ozlem Kucuk, Elif Çıngı Özdemir, Elena Castro, Emre Yekedüz, Yüksel Ürün","doi":"10.1016/j.ejca.2025.115226","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Cabazitaxel and <sup>177</sup>Lu-PSMA-617 have been shown to improve survival in patients with metastatic castration-resistant prostate cancer (mCRPC) previously treated with docetaxel and androgen receptor pathway inhibitors (ARPI). we aimed to evaluate the impact of sequencing cabazitaxel and <sup>177</sup>Lu-PSMA-617 on survival outcomes in patients with mCRPC.</p><p><strong>Patients and methods: </strong>This is a retrospective, multicenter, cohort study which included patients with mCRPC who received sequential treatment with <sup>177</sup>Lu-PSMA-617 and cabazitaxel between January 2015 and December 2023. Primary outcome was progression-free survival-2 (PFS-2) RESULTS: A total of 68 patients with mCRPC who received sequential <sup>177</sup>Lu-PSMA-617 and cabazitaxel were included in the study. The primary outcome, progression-free survival-2 (PFS-2), was similar in patients treated with <sup>177</sup>Lu-PSMA-617 first (LU-CA) and those receiving cabazitaxel (CA-LU) first (10.8 and 11.7 months, respectively; p = 0.422). The median overall survival (OS) was also similar in the LU-CA and CA-LU groups (16.6 and 19.9 months, respectively; p = 0.917). The objective response rate (ORR) for <sup>177</sup>Lu-PSMA-617 was 23.1 % when used first and 16.1 % after cabazitaxel. ORR for cabazitaxel was 25.6 % and 31.3 % when used as the first agent and when used after <sup>177</sup>Lu-PSMA-617, respectively.</p><p><strong>Conclusions: </strong>In conclusion, treatment sequencing between cabazitaxel and <sup>177</sup>Lu-PSMA-617 did not significantly affect survival outcomes in patients with mCRPC. These findings suggest that both drugs can be effectively integrated into the mCRPC treatment paradigm without concerns about the effect of sequencing. However, prospective data are needed to optimize sequencing strategies and explore their impact on specific patient subgroups for more personalized care.</p>","PeriodicalId":11980,"journal":{"name":"European Journal of Cancer","volume":"217 ","pages":"115226"},"PeriodicalIF":7.6000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparison of two alternative sequences with cabazitaxel and 177Lu-PSMA-617 in metastatic castration-resistant prostate cancer: A retrospective multicenter study (LuCaS).\",\"authors\":\"Hatice Bolek, Satı Coskun Yazgan, Furkan Ceylan, Jorge Esteban-Villarrubia, Cagatay Arslan, Tülay Kuş, Deniz Tural, Mehmet Ali Nahit Sendur, Nuriye Ozlem Kucuk, Elif Çıngı Özdemir, Elena Castro, Emre Yekedüz, Yüksel Ürün\",\"doi\":\"10.1016/j.ejca.2025.115226\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Cabazitaxel and <sup>177</sup>Lu-PSMA-617 have been shown to improve survival in patients with metastatic castration-resistant prostate cancer (mCRPC) previously treated with docetaxel and androgen receptor pathway inhibitors (ARPI). we aimed to evaluate the impact of sequencing cabazitaxel and <sup>177</sup>Lu-PSMA-617 on survival outcomes in patients with mCRPC.</p><p><strong>Patients and methods: </strong>This is a retrospective, multicenter, cohort study which included patients with mCRPC who received sequential treatment with <sup>177</sup>Lu-PSMA-617 and cabazitaxel between January 2015 and December 2023. Primary outcome was progression-free survival-2 (PFS-2) RESULTS: A total of 68 patients with mCRPC who received sequential <sup>177</sup>Lu-PSMA-617 and cabazitaxel were included in the study. The primary outcome, progression-free survival-2 (PFS-2), was similar in patients treated with <sup>177</sup>Lu-PSMA-617 first (LU-CA) and those receiving cabazitaxel (CA-LU) first (10.8 and 11.7 months, respectively; p = 0.422). The median overall survival (OS) was also similar in the LU-CA and CA-LU groups (16.6 and 19.9 months, respectively; p = 0.917). The objective response rate (ORR) for <sup>177</sup>Lu-PSMA-617 was 23.1 % when used first and 16.1 % after cabazitaxel. ORR for cabazitaxel was 25.6 % and 31.3 % when used as the first agent and when used after <sup>177</sup>Lu-PSMA-617, respectively.</p><p><strong>Conclusions: </strong>In conclusion, treatment sequencing between cabazitaxel and <sup>177</sup>Lu-PSMA-617 did not significantly affect survival outcomes in patients with mCRPC. These findings suggest that both drugs can be effectively integrated into the mCRPC treatment paradigm without concerns about the effect of sequencing. However, prospective data are needed to optimize sequencing strategies and explore their impact on specific patient subgroups for more personalized care.</p>\",\"PeriodicalId\":11980,\"journal\":{\"name\":\"European Journal of Cancer\",\"volume\":\"217 \",\"pages\":\"115226\"},\"PeriodicalIF\":7.6000,\"publicationDate\":\"2025-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ejca.2025.115226\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Cancer","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ejca.2025.115226","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:卡巴他赛和177Lu-PSMA-617已被证明可以提高转移性去势抵抗性前列腺癌(mCRPC)患者的生存率,这些患者此前曾接受过多西紫杉醇和雄激素受体途径抑制剂(ARPI)的治疗。我们旨在评估卡巴他赛和177Lu-PSMA-617测序对mCRPC患者生存结局的影响。患者和方法:这是一项回顾性、多中心、队列研究,纳入了2015年1月至2023年12月期间接受177Lu-PSMA-617和卡巴他赛序贯治疗的mCRPC患者。结果:共有68例接受序贯177Lu-PSMA-617和卡巴他赛治疗的mCRPC患者被纳入研究。首先接受177Lu-PSMA-617 (LU-CA)治疗的患者和首先接受卡巴他赛(CA-LU)治疗的患者的主要终点无进展生存期-2 (PFS-2)相似(分别为10.8和11.7个月; = 0.422页)。LU-CA和CA-LU组的中位总生存期(OS)也相似(分别为16.6个月和19.9个月; = 0.917页)。177Lu-PSMA-617的客观缓解率(ORR)在首次使用时为23.1% %,在卡巴他赛后为16.1% %。卡巴他赛作为第一种药物和在177Lu-PSMA-617治疗后使用时的ORR分别为25.6 %和31.3 %。结论:总之,卡巴他赛和177Lu-PSMA-617的治疗顺序对mCRPC患者的生存结局没有显著影响。这些发现表明,这两种药物都可以有效地整合到mCRPC治疗模式中,而无需担心测序的影响。然而,需要前瞻性数据来优化测序策略并探索其对特定患者亚组的影响,以实现更个性化的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of two alternative sequences with cabazitaxel and 177Lu-PSMA-617 in metastatic castration-resistant prostate cancer: A retrospective multicenter study (LuCaS).

Background: Cabazitaxel and 177Lu-PSMA-617 have been shown to improve survival in patients with metastatic castration-resistant prostate cancer (mCRPC) previously treated with docetaxel and androgen receptor pathway inhibitors (ARPI). we aimed to evaluate the impact of sequencing cabazitaxel and 177Lu-PSMA-617 on survival outcomes in patients with mCRPC.

Patients and methods: This is a retrospective, multicenter, cohort study which included patients with mCRPC who received sequential treatment with 177Lu-PSMA-617 and cabazitaxel between January 2015 and December 2023. Primary outcome was progression-free survival-2 (PFS-2) RESULTS: A total of 68 patients with mCRPC who received sequential 177Lu-PSMA-617 and cabazitaxel were included in the study. The primary outcome, progression-free survival-2 (PFS-2), was similar in patients treated with 177Lu-PSMA-617 first (LU-CA) and those receiving cabazitaxel (CA-LU) first (10.8 and 11.7 months, respectively; p = 0.422). The median overall survival (OS) was also similar in the LU-CA and CA-LU groups (16.6 and 19.9 months, respectively; p = 0.917). The objective response rate (ORR) for 177Lu-PSMA-617 was 23.1 % when used first and 16.1 % after cabazitaxel. ORR for cabazitaxel was 25.6 % and 31.3 % when used as the first agent and when used after 177Lu-PSMA-617, respectively.

Conclusions: In conclusion, treatment sequencing between cabazitaxel and 177Lu-PSMA-617 did not significantly affect survival outcomes in patients with mCRPC. These findings suggest that both drugs can be effectively integrated into the mCRPC treatment paradigm without concerns about the effect of sequencing. However, prospective data are needed to optimize sequencing strategies and explore their impact on specific patient subgroups for more personalized care.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
European Journal of Cancer
European Journal of Cancer 医学-肿瘤学
CiteScore
11.50
自引率
4.80%
发文量
953
审稿时长
23 days
期刊介绍: The European Journal of Cancer (EJC) serves as a comprehensive platform integrating preclinical, digital, translational, and clinical research across the spectrum of cancer. From epidemiology, carcinogenesis, and biology to groundbreaking innovations in cancer treatment and patient care, the journal covers a wide array of topics. We publish original research, reviews, previews, editorial comments, and correspondence, fostering dialogue and advancement in the fight against cancer. Join us in our mission to drive progress and improve outcomes in cancer research and patient care.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信