肌肉浸润性膀胱癌患者新辅助化疗联合免疫疗法的疗效和安全性分析。

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2024-11-01 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1479743
Yanhang Yu, Chuanao Zhang, Hao Chen, Jianglei Zhang, Jun Ouyang, Zhiyu Zhang
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引用次数: 0

摘要

简介:本研究探讨了肌层浸润性膀胱癌(MIBC)患者新辅助化疗联合免疫疗法的有效性和安全性:本研究探讨了肌层浸润性膀胱癌(MIBC)患者新辅助化疗联合免疫治疗的有效性和安全性:这项回顾性队列研究纳入了2020年1月1日至2023年12月31日期间在苏州大学附属第一医院确诊的肌浸润性膀胱癌患者,根据新辅助治疗方案分配到化疗组(吉西他滨加顺铂)或联合治疗组(化疗加托利帕利单抗或替舒利珠单抗)。比较了各组间的关键指标,包括病理分期率(PDR)、病理完全反应率(PCRR)以及不良事件(AE)的发生率和严重程度:本研究共纳入 53 例患者(平均年龄 67.21 岁)。在联合治疗组中,14 名患者(51.85%)获得病理完全缓解(ypT0),7 名患者(25.93%)获得部分缓解(ypT1),PDR 和 PCRR 分别为 77.78% 和 51.85%。化疗组中,6 名患者(23.08%)获得完全缓解,5 名患者(19.23%)获得部分缓解,PDR 和 PCRR 分别为 42.31% 和 23.08%。组间差异具有统计学意义(P < 0.05)。在联合用药组中,各亚组的病理分期或完全缓解率无明显差异(P > 0.05)。两组患者均未发现严重过敏反应或致命性不良反应,也未出现 4 级不良反应。联合组和化疗组的3级AE发生率分别为22.22%和20.83%,但不显著(P > 0.05):结论:新辅助化疗联合免疫疗法在MIBC患者中具有更高的疗效和可控的安全性,这表明其有可能被纳入临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety analysis of neoadjuvant chemotherapy combined with immunotherapy in patients with muscle-invasive bladder cancer.

Introduction: This study examined the efficacy and safety of neoadjuvant chemotherapy combined with immunotherapy in patients with muscle-invasive bladder cancer (MIBC).

Methods: This retrospective cohort study included patients diagnosed with MIBC at the First Affiliated Hospital of Soochow University between January 1, 2020, and December 31, 2023, assigned to either chemotherapy (gemcitabine with cisplatin) or combination (chemotherapy plus toripalimab or tislelizumab) groups based on the neoadjuvant treatment regimen. Key metrics, including pathological downstaging rate (PDR), pathological complete response rate (PCRR), and incidence and severity of adverse events (AEs), were compared between groups.

Results: This study included 53 patients (mean age: 67.21 years). In the combination group, 14 patients (51.85%) achieved pathological complete remission (ypT0), and seven (25.93%) achieved partial remission (ypT1), resulting in a PDR and PCRR of 77.78 and 51.85%, respectively. In the chemotherapy group, six patients (23.08%) achieved complete remission, and five (19.23%) achieved partial remission, resulting in a PDR and PCRR of 42.31 and 23.08%, respectively. Differences between groups were statistically significant (p < 0.05). There were no significant differences in pathological downstaging or complete remission rates among subgroups in the combination group (p > 0.05). No serious allergic reactions or fatal AEs were detected in either group, with no grade 4 AEs. Grade 3 AE rates were 22.22 and 20.83% in the combination and chemotherapy groups, respectively, although non-significant (p > 0.05).

Conclusion: Neoadjuvant chemotherapy combined with immunotherapy had enhanced efficacy and manageable safety in patients with MIBC, suggesting its potential for integration into clinical practice.

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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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