关于符合铂金条件的局部晚期或转移性尿路上皮癌患者的铂金资格和治疗顺序的播客。

IF 4.4 3区 医学 Q2 ONCOLOGY
Targeted Oncology Pub Date : 2024-07-01 Epub Date: 2024-07-04 DOI:10.1007/s11523-024-01074-9
Shilpa Gupta, Helen H-S Moon, Srikala S Sridhar
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引用次数: 0

摘要

晚期尿路上皮癌患者的治疗形势在不断变化。Enfortumab vedotin加pembrolizumab已获得美国食品药品管理局的批准,因为最近的3期试验数据显示,与一线铂类化疗相比,该疗法疗效更优;然而,其独特的毒性特征可能使其不太适合某些患者,而且在一些国家的供应可能会受到成本因素的限制。因此,预计铂类化疗仍将是重要的一线治疗方案。铂类方案(顺铂或卡铂为基础)的选择取决于对临床特征的评估,包括表现状态、肾功能、是否存在周围神经病变或心力衰竭。对于完成铂类化疗后未出现疾病进展的患者,国际指南推荐采用阿维单抗一线维持治疗。对于疾病进展的患者,pembrolizumab 是首选方法。此外,根据最近一项三期试验的结果,nivolumab 加顺铂化疗也获得了美国食品和药物管理局的批准,成为符合顺铂条件的患者的另一种一线治疗选择。晚期尿路上皮癌患者的后线治疗方案取决于先前的治疗,可能包括恩福单抗维多汀、厄达非尼(适用于FGFR2/3突变或融合/重排患者)、sacituzumab govitecan和铂再挑战。对于一小部分不符合任何铂类化疗条件的患者(即不适合顺铂或卡铂),使用pembrolizumab或atezolizumab的免疫检查点抑制剂单药治疗是一线治疗选择,但各国批准的药物有所不同。总之,本期播客讨论了晚期尿路上皮癌治疗领域的最新进展、接受铂类化疗的资格、潜在的一线治疗方案以及治疗排序。补充文件1(MP4 246907 KB)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Podcast on Platinum Eligibility and Treatment Sequencing in Platinum-Eligible Patients with Locally Advanced or Metastatic Urothelial Carcinoma.

The treatment landscape for patients with advanced urothelial carcinoma continues to evolve. Enfortumab vedotin plus pembrolizumab has received Food and Drug Administration approval based on recent phase 3 trial data showing superior efficacy compared with first-line platinum-based chemotherapy; however, its distinct toxicity profile may make it less suitable for some patients, and availability in some countries may be limited by cost considerations. Consequently, platinum-based chemotherapy is expected to remain an important first-line treatment option. Choice of platinum regimen (cisplatin- or carboplatin-based) is informed by assessment of clinical characteristics, including performance status, kidney function, and presence of peripheral neuropathy or heart failure. For patients without disease progression after completing platinum-based chemotherapy, avelumab first-line maintenance treatment is recommended by international guidelines. For patients who have disease progression, pembrolizumab is the preferred approach. Additionally, following results from a recent phase 3 trial, nivolumab plus cisplatin-based chemotherapy has also received Food and Drug Administration approval and is an additional first-line treatment option for cisplatin-eligible patients. Later-line options for patients with advanced urothelial carcinoma, depending on prior treatment, may include enfortumab vedotin, erdafitinib (for patients with FGFR2/3 mutations or fusions/rearrangements), sacituzumab govitecan, and platinum rechallenge. For the small proportion of patients ineligible for any platinum-based chemotherapy (i.e., unsuitable for cisplatin or carboplatin), immune checkpoint inhibitor monotherapy with pembrolizumab or atezolizumab is a first-line treatment option, although approved agents vary between countries. In summary, this podcast discusses recent developments in the treatment landscape for advanced urothelial carcinoma, eligibility for platinum-based chemotherapy, potential first-line treatment options, and treatment sequencing. Supplementary file1 (MP4 246907 KB).

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来源期刊
Targeted Oncology
Targeted Oncology 医学-肿瘤学
CiteScore
8.40
自引率
3.70%
发文量
64
审稿时长
>12 weeks
期刊介绍: Targeted Oncology addresses physicians and scientists committed to oncology and cancer research by providing a programme of articles on molecularly targeted pharmacotherapy in oncology. The journal includes: Original Research Articles on all aspects of molecularly targeted agents for the treatment of cancer, including immune checkpoint inhibitors and related approaches. Comprehensive narrative Review Articles and shorter Leading Articles discussing relevant clinically established as well as emerging agents and pathways. Current Opinion articles that place interesting areas in perspective. Therapy in Practice articles that provide a guide to the optimum management of a condition and highlight practical, clinically relevant considerations and recommendations. Systematic Reviews that use explicit, systematic methods as outlined by the PRISMA statement. Adis Drug Reviews of the properties and place in therapy of both newer and established targeted drugs in oncology.
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