Evidence map›Paper›PMID 41495002›Full record

ArticleThe oncologist2026

An increase in splenic volume after first-line immunotherapy is associated with worse PFS in patients with metastatic renal cell carcinoma.

Gregory Palmateer, Ahmet Yildirim, Taylor Goodstein, Dattatraya Patil, Samay Patel, Shreyas Joshi, Vikram Narayan, Jacqueline T Brown, Bassel Nazha, Shahid S Ahmed and 7 more

Abstract read
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Article in The oncologist, 2026. 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

What it found

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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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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Gregory PalmateerDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Ahmet YildirimDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.ORCID 0009-0006-2542-3714
Taylor GoodsteinDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.ORCID 0000-0001-5062-5461
Dattatraya PatilDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Samay PatelDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Shreyas JoshiDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Vikram NarayanDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Jacqueline T BrownDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Bassel NazhaDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Shahid S AhmedDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Jordan CiuroDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Bradley C CarthonDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Omer KucukDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Haydn KissickDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Kenneth OganDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Mehmet A BilenDepartment of Hematology and Oncology, Emory University School of Medicine, Atlanta, GA 30322, United States.ORCID 0000-0003-4003-1103
Viraj A MasterDepartment of Urology, Emory University School of Medicine, Atlanta, GA 30322, United States.ORCID 0000-0002-7251-142X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceReliable prognostic markers for immune checkpoint inhibitor (ICI) response in metastatic renal cell carcinoma (mRCC) remain limited.

objectiveTo examine the impact of splenic volume change after ICI initiation on progression-free survival (PFS) and overall survival (OS) in patients with mRCC.

designA retrospective cohort study reviewing data from 2015 to 2023.

settingThe Emory Kidney Cancer database (single-center academic instution).

participantsPatients with mRCC who underwent first-line ICI treatment and had available abdominal imaging 30 days before and 60-120 days after ICI initiation. A total of 109 patients met inclusion criteria. EXPOSURE: Splenic volume change calculated as a percentage difference between baseline and follow-up imaging (median 2.8 months post-initiation) using a standardized formula, grouped into ≥10% increase and <10% increase. MAIN OUTCOMES AND MEASURES: Differences in OS and PFS assessed using Kaplan-Meier curves and multivariable Cox hazards regression models.

resultsA total of 109 patients met inclusion criteria. Median follow-up time was 25.2 months (IQR 11.2-41.5), during which there were 47 mortality events. Patients with a splenic volume increase ≥ 10% at a median 2.8 months after ICI initiation had worse 2-year PFS (28.5% vs 50.4%, P = .022) but not OS (69.4% vs 77.8%, P = .853) compared to patients with a < 10% increase in splenic volume. On multivariable analysis, a splenic volume increase ≥ 10% was independently associated with worse PFS (2.33 [95% CI 1.37-3.96], P = .002). CONCLUSIONS AND RELEVANCE: In patients with mRCC, a splenic volume increase ≥ 10% at a median of 2.8 months following ICI initiation is independently associated with worse survival compared to an < 10% increase. Monitoring splenic volume changes may serve as a cost-effective radiographic prognostic marker to guide treatment sequencing.

Indexed as

Carcinoma, Renal CellImmune Checkpoint InhibitorsImmunotherapyKidney NeoplasmsSpleenAgedFemaleHumansMaleMiddle AgedPrognosisProgression-Free SurvivalRetrospective StudiesImmune Checkpoint Inhibitorsimmuno-oncologyimmunotherapyradiologic biomarkersrenal cell carcinomasplenic change

Identifiers

PMID41495002
PMCPMC12828282

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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.