Evidence map›Paper›PMID 40940250›Full record

ArticleUrologic oncology2026

Long-term oncologic outcomes of metastatic clear-cell renal cell carcinoma after local therapy alone.

Daniel Barbakoff, Mark T Dawidek, Andrea Knezevic, Marc Ganz, Lina Posada, Yash Khandwala, Andrea Lopez Sanmiguel, Stephen W Reese, Arnold Oparanozie, Nicole Liso and 8 more

Abstract read
In one paragraph

Article in Urologic oncology, 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

18 authors.

Daniel BarbakoffDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Mark T DawidekDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Andrea KnezevicDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Marc GanzDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Lina PosadaDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Yash KhandwalaDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Andrea Lopez SanmiguelDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Stephen W ReeseDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Arnold OparanozieDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Nicole LisoDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Ritesh R KotechaDepartment of Genitourinary Medical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
Robert J MotzerDepartment of Genitourinary Medical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
Ed ReznikDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Jonathan ColemanDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
Irina OstrovnayaDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Martin H VossDepartment of Genitourinary Medical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
Paul RussoDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY.
A Ari HakimiDepartment of Urology, Memorial Sloan Kettering Cancer Center, New York, NY. Electronic address: hakimia@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeOligometastatic clear-cell renal cell carcinoma (ccRCC) represents a heterogeneous entity that can, in select cases, be managed with primary tumor resection and complete local treatment at all metastatic sites, rendering a patient metastatic with no evidence of disease (M1 NED). M1 NED patients have improved overall survival, although previous cohorts are relatively small and heterogeneous. We sought to identify the natural history of M1 NED ccRCC to clinical trial findings and to optimize management strategies. MATERIALS AND

methodsPatients with synchronous metastatic ccRCC treated with local therapy alone and considered radiographically M1 NED at our institution between 1989 and 2023 were retrospectively evaluated. Survival probabilities used a combination of Kaplan-Meier estimator, log-rank test, and multivariable Cox proportional hazards regression. When available, limited genomic data obtained using the MSK-IMPACT targeted panel was correlated with outcomes.

results85 patients met inclusion criteria. One-year disease free survival (DFS) was 53% (95% CI: 42 to 63%). Sarcomatoid features predicted shorter DFS (HR 2.62, CI: 1.08, 6.34, P = 0.03). Time from first disease recurrence to second recurrence was longer among patients with initial DFS ≥2 years (median 42 vs. 15 months, log-rank P = 0.005). A total of 18 patients (21%) underwent targeted genomic sequencing; higher fraction of genome altered and CDKN2A copy number loss were associated with shorter DFS. Findings were limited by cohort size.

conclusionsMost M1 NED ccRCC patients will experience disease recurrence, although certain baseline risk factors appear to predict earlier recurrence. Prognostic biomarkers are needed to predict outcomes and facilitate patient management.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeClear cell renal cell carcinomaComplete metastasectomyM1 NED

Identifiers

PMID40940250
PMCPMC12614635

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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.