Evidence map›Paper›PMID 42665381›Full record

ArticleIn vivo (Athens, Greece)

Real-world Feasibility of Adjuvant Nivolumab for High-risk Upper Tract Urothelial Carcinoma After Radical Nephroureterectomy.

Masaaki Yanishi, Jun Matsushita, Akiyo Kita, Takao Mishima, Hidefumi Kinoshita

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Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Masaaki YanishiDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan masaaki.yanishi@gmail.com.
Jun MatsushitaDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan.
Akiyo KitaDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan.
Takao MishimaDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan.
Hidefumi KinoshitaDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimAdjuvant nivolumab is an important postoperative option for high-risk muscle-invasive urothelial carcinoma, but upper tract urothelial carcinoma (UTUC)-specific real-world evidence remains limited. This study evaluated oncologic outcomes, feasibility, and safety of adjuvant nivolumab after radical nephroureterectomy in patients with high-risk UTUC. PATIENTS AND

methodsWe retrospectively analyzed 21 consecutive patients with high-risk UTUC who received adjuvant nivolumab at the Kansai Medical University group between April 2022 and March 2025. Metastasis-free survival (MFS), overall survival (OS), treatment completion, and treatment-related adverse events (AEs) were assessed. Survival was estimated using the Kaplan-Meier method.

resultsThe median age was 76 years, and 14 patients (66.7%) had received neoadjuvant chemotherapy. The median follow-up from nivolumab initiation was 744 days. Median MFS and OS were not reached. The 12- and 24-month MFS rates were both 80.1%, while the 12- and 24-month OS rates were 90.0% and 84.4%, respectively. The median treatment duration was 34 weeks, and 10 patients (47.6%) completed the planned 48-week course. Any treatment-related AE occurred in nine patients (42.9%), and seven discontinued treatment because of grade 3 AEs.

conclusionThis early real-world study suggests that adjuvant nivolumab is feasible and may provide favorable short-term disease control in selected patients with high-risk UTUC after radical nephroureterectomy. These findings support its potential role as a postoperative option for selected patients, particularly when delivery of additional platinum-based therapy is difficult.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Transitional CellNephroureterectomyNivolumabUrologic NeoplasmsAgedAged, 80 and overChemotherapy, AdjuvantFeasibility StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntineoplastic Agents, ImmunologicalNivolumabadjuvant nivolumabmetastasis-free survivalnephroureterectomyreal-world studyUpper tract urothelial carcinoma

Identifiers

PMID42665381
PMCPMC13531098

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.