Evidence map›Paper›PMID 41341717›Full record

ArticleEuropean urology open science2026

Outcomes After Initial Noninterventional Management of Clinical Stage cT1b Renal Masses.

Banna Hussain, Jack Considine, Yuzhi Wang, Brian R Lane, Sami Wilder, Mohit Butaney, Stephanie Daignault-Newton, Monica Van Til, Abena Osei, Mackenzie Gammons and 4 more

Abstract read
In one paragraph

Article in European urology open science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Banna HussainVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.
Jack ConsidineVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.
Yuzhi WangVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.
Brian R LaneDivision of Urology, Corewell Health West, Grand Rapids, MI, USA.
Sami WilderVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.
Mohit ButaneyVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.
Stephanie Daignault-NewtonDepartment of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Monica Van TilDepartment of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Abena OseiMichigan State University College of Human Medicine, Grand Rapids, MI, USA.
Mackenzie GammonsDepartment of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Mahin MirzaDepartment of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Alice SemerjianDepartment of Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Craig G RogersVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.
Amit K PatelVattikuti Urology Institute, Henry Ford Health, Detroit, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objective: Localized renal masses 4.1-7.0 cm in size (cT1bRMs) are typically treated with partial or radical nephrectomy. Utilization and results of initial nonsurgical approaches for cT1bRMs are unclear. Our primary objective was to evaluate overall (OS) and metastasis-free (MFS) survival after initiating surveillance for cT1bRMs. Methods: We retrospectively examined initial management and subsequent follow-up of all patients diagnosed with cT1bRMs (from May 2017 to November 2024) in the Michigan Urological Surgery Improvement Collaborative (MUSIC). Patients were stratified by intervention versus surveillance at 90 d following initial consultation. Patients initiating surveillance were further stratified as those with continued surveillance versus delayed intervention (DI) at least 90 d after initiating surveillance. The 3-yr estimated rates of DI, OS, MFS, and cancer-specific survival (CSS) were reported. Key findings and limitations: Of 1134 patients with cT1bRMs, 297 were initiated on surveillance (26%), including 207 (70%) with solid, 47 (16%) with Bosniak III/IV, and 43 (14%) with indeterminate lesions. In a multivariable analysis, the predictors of surveillance included Charlson Comorbidity Index ≥2 versus 0 (odds ratio [OR] 1.43, 95% confidence interval [CI] 0.97-2.13), nonsolid tumor type (Bosniak III/IV cyst: OR 8.03, 95% CI 4.58-14; indeterminate: OR 5.42, 95% CI 2.86-10.3), and benign findings on a renal mass biopsy (OR 24.0, 95% CI 9.07-63). For the 297 surveilled cT1bRM patients, the cumulative incidence of DI at 2 yr was 27%, and the rates of MFS, CSS, and OS were, respectively, 91%, 96%, and 84% at 3 yr after initiating surveillance. A subset analysis excluding cystic, indeterminate, and biopsy-proven benign tumors found the cumulative incidence of DI at 2 yr to be 35%, with MFS and OS rates to be 95% and 78%, respectively, at 3 yr. In a multivariable analysis, initial surveillance was not associated with OS (vs immediate treatment; hazard ratio [HR] 1.47, 95% CI 0.83-2.63), with age as the only significant factor (HR 1.31, 95% CI 1.16-1.48). Limitations include the study's observational and retrospective nature. Conclusions and clinical implications: The MUSIC data support active surveillance for select patients with cT1bRMs. Patient summary: In this report, we looked at the outcomes of surveilling larger (cT1b) renal masses in a large population in Michigan. We found that watching instead of treating cT1b renal masses immediately in older people with more medical conditions did not change survival or cause the cancer to spread compared with people who were treated immediately. We conclude that surveillance for cT1b cancer is an option that should be considered for all patients but implemented selectively.

Indexed as

Active surveillancecT1b kidney cancerRenal cancer

Identifiers

PMID41341717
PMCPMC12670937

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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.