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[膀胱癌免疫疗法的未来走向?当前试验与进展的最新情况]

[Immunotherapy in bladder cancer-quo vadis? Update on current trials and developments].

作者信息

Todenhöfer T, Boegemann M

机构信息

Studienpraxis Urologie, Nürtingen, Deutschland.

Klinik für Urologie und Kinderurologie, Universitätsklinikum Münster, Albert-Schweitzer-Campus 1 GB A1, 48149, Münster, Deutschland.

出版信息

Urologe A. 2020 Jul;59(7):810-816. doi: 10.1007/s00120-020-01237-2.

Abstract

BACKGROUND

Great advances have been made for the treatment of urothelial carcinoma by the introduction of checkpoint inhibitors (CPI). Single-agent immunotherapy with CPIs has been approved for patients with metastatic or locally advanced inoperable urothelial carcinoma who have either progressed during or after platinum-based chemotherapy or who are cisplatin-ineligible. For cisplatin-ineligible patients, approval is restricted to patients with high programmed cell death ligand 1 (PD-L1) expression. For patients with nonmuscle invasive bladder cancer (NMIBC) or patients with muscle invasive bladder cancer (MIBC) who receive curative therapy, no CPIs have received approval in Germany.

OBJECTIVES

To provide an overview of the current landscape of immunotherapy in patients with urothelial carcinoma.

METHODS

Summary of the therapeutic landscape and resulting challenges based on currently published data using a PubMed search.

RESULTS

In the treatment of metastatic or inoperable urothelial carcinoma, CPIs represent standard treatment. Depending on the results of currently performed trials, an extension of its use to the perioperative setting (neoadjuvant/adjuvant) and to patients with Bacillus Calmette Guérin (BCG) unresponsive NMIBC in the near future is currently being discussed.

CONCLUSIONS

Immuno-oncologic treatment using CPIs has become an integral part of the management of patients with advanced bladder cancer. For biomarker-based patient selection and combination therapies, there is an urgent need for further investigations within clinical trial protocols.

摘要

背景

通过引入检查点抑制剂(CPI),尿路上皮癌的治疗取得了巨大进展。单药免疫疗法已被批准用于铂类化疗期间或之后病情进展或不符合顺铂治疗条件的转移性或局部晚期不可手术切除的尿路上皮癌患者。对于不符合顺铂治疗条件的患者,批准仅限于程序性细胞死亡配体1(PD-L1)高表达的患者。在德国,对于接受根治性治疗的非肌层浸润性膀胱癌(NMIBC)患者或肌层浸润性膀胱癌(MIBC)患者,尚无CPI获得批准。

目的

概述尿路上皮癌患者免疫治疗的现状。

方法

基于目前发表的数据,通过PubMed搜索总结治疗现状及由此产生的挑战。

结果

在转移性或不可手术切除的尿路上皮癌治疗中,CPI是标准治疗方法。根据目前正在进行的试验结果,目前正在讨论在不久的将来将其应用扩展到围手术期(新辅助/辅助)以及卡介苗(BCG)无反应的NMIBC患者。

结论

使用CPI的免疫肿瘤治疗已成为晚期膀胱癌患者管理的一个组成部分。对于基于生物标志物的患者选择和联合治疗,迫切需要在临床试验方案内进行进一步研究。

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