派姆单抗治疗晚期尿路上皮癌患者的预后免疫治疗评分(PIS):真实世界数据和ARON-2数据集的验证

IF 3.2 3区 医学 Q2 ONCOLOGY
Alessandro Rizzo, Anas Zayed, Elsa Vitale, Sebastiano Buti, Hideki Takeshita, Simon Crabb, Giandomenico Roviello, Emmanuel Seront, Jose Carlos Tapia, Sarah Scagliarini, Lazar Popovic, Ray Manneh Kopp, Halima Abahssain, Mimma Rizzo, Fernando Sabino Marques Monteiro, Raffaella Massafra, Oronzo Brunetti, Daniele Santini, Yüksel Ürün, Rodolfo Montironi, Veronica Mollica, Francesco Massari, Andrey Soares, Matteo Santoni
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引用次数: 0

摘要

近年来,基于免疫治疗的新型组合策略的发展和出现,基于免疫检查点抑制剂(ICI)的治疗已经成为转移性尿路上皮癌(UC)治疗的主要方法。在此,我们旨在验证先前开发的评分,预后免疫治疗评分(PIS)的预后价值,包括女性性别,东部合作肿瘤组性能状态(ECOG-PS)和肝转移,来自ARON-2数据集的派姆单抗治疗晚期UC的患者。我们回顾性分析了年龄≥18岁的转移性UC患者的临床资料。在2016年1月1日至2023年12月31日期间,来自21个国家的68个肿瘤中心纳入了在铂基治疗后进展或复发的患者,并接受了派姆单抗治疗。Kaplan-Meier分析计算中位随访时间。采用Cox比例风险模型比较多变量对患者生存的影响,并计算风险比(hr)和95%置信区间(ci)。对存在0、1或≥2个危险因素分层的患者的OS和PFS,以及按年龄、肿瘤组织学、部位和转移性疾病时间分层的患者的OS与0、1或≥2个危险因素的患者进行生存受体工作特征(ROC)分析。亚组间比较采用Fisher精确检验。我们从ARON-2数据集中纳入了1040名患者。我们进一步根据先前公布的三个危险因素对患者进行分层:女性、ECOG-PS = 2和肝转移;526例(51%)患者危险因素为0,408例(39%)患者危险因素为1,106例(10%)患者危险因素≥2。在单因素和多因素分析中,骨转移、同步转移性疾病和我们基于女性的PIS模型、肝转移和运动状态不佳与OS和PFS均显著相关。我们的研究结果验证了PIS是一种实用的评分模型,使用性别、ECOG-PS和肝转移来分层派姆单抗治疗的晚期尿路上皮癌的生存结果,支持更个性化的治疗决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic immunotherapy score (PIS) in patients with advanced urothelial carcinoma treated with pembrolizumab: real-world data and validation from ARON-2 dataset.

Recent years have seen the development and advent of novel combinatorial strategies based on immunotherapy, and immune checkpoint inhibitor (ICI) - based treatment has established itself as a mainstay in the treatment of metastatic urothelial carcinoma (UC). Herein, we aimed to validate the prognostic value of a previously developed score, the Prognostic Immunotherapy Score (PIS), including female sex, Eastern Cooperative Oncology Group Performance Status (ECOG-PS) and liver metastases, in patients treated with pembrolizumab for advanced UC from the ARON-2 dataset. We retrospectively analyzed clinical data from Metastatic UC patients diagnosed at age ≥ 18 years. Patients progressing or recurring after platinum-based therapy were included, and treated with pembrolizumab from January 1st, 2016, to December 31st, 2023, in 68 oncological centers from 21 Countries. The Kaplan-Meier analysis was used to calculate the median follow-up. Cox proportional hazard models were used to compare the multivariable effects on patients' survival and to calculate hazard ratios (HRs) and 95% confidence intervals (CIs). A survival receiver operating characteristic (ROC) analysis was exploited in relation to OS and PFS in patients stratified by the presence of 0, 1 or ≥ 2 risk factors and OS with 0, 1 or ≥ 2 risk factors in patients stratified by age, tumor histology, site and time to metastatic disease. The comparison between subgroups was performed with the Fisher exact test. We included 1040 patients from the ARON-2 dataset. We further stratified patients based on the three previously published risk factors: female sex, ECOG-PS = 2 and liver metastases; 526 patients (51%) had 0 risk factors, 408 patients (39%) had 1 factor and 106 patients (10%) had ≥ 2 risk factors. At univariate and multivariate analyses, bone metastases, synchronous metastatic disease and our PIS model based on female sex, liver metastasis, and poor performance status were significantly associated with both OS and PFS. Our findings validate the PIS as a practical scoring model using sex, ECOG-PS, and liver metastasis to stratify survival outcomes in advanced urothelial carcinoma treated with pembrolizumab, supporting more personalized treatment decisions.

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来源期刊
CiteScore
7.80
自引率
5.00%
发文量
55
审稿时长
12 months
期刊介绍: The Journal''s scope encompasses all aspects of metastasis research, whether laboratory-based, experimental or clinical and therapeutic. It covers such areas as molecular biology, pharmacology, tumor biology, and clinical cancer treatment (with all its subdivisions of surgery, chemotherapy and radio-therapy as well as pathology and epidemiology) insofar as these disciplines are concerned with the Journal''s core subject of metastasis formation, prevention and treatment.
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