Evidence map›Paper›PMID 39898813›Full record

ArticleJournal of the National Cancer Institute2025

Factors associated with longitudinal progression of the cumulative burden of morbidity and overall mortality after cisplatin-based chemotherapy for testicular cancer.

Sarah L Kerns, Paul C Dinh, Patrick O Monahan, Timothy Stump, Chunkit Fung, Howard D Sesso, Darren R Feldman, Robert J Hamilton, David J Vaughn, Robert Huddart and 6 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

16 authors.

Sarah L KernsDepartment of Radiation Oncology, Medical College of Wisconsin, Milwaukee, WI, United States.ORCID 0000-0002-6503-0011
Paul C DinhDivision of Medical Oncology, Indiana University School of Medicine, Indianapolis, IN, United States.
Patrick O MonahanDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, IN, United States.
Timothy StumpDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, IN, United States.ORCID 0000-0001-9593-3011
Chunkit FungJ.P. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, United States.ORCID 0000-0002-9384-0732
Howard D SessoDivision of Preventive Medicine, Brigham and Women's Hospital, Boston, MA, United States.ORCID 0000-0002-9698-9954
Darren R FeldmanMemorial Sloan Kettering Cancer Center, New York, NY, United States.ORCID 0000-0003-2424-4635
Robert J HamiltonDivision of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-6715-5934
David J VaughnDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Robert HuddartThe Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London, United Kingdom.ORCID 0000-0003-3604-1990
Christian KollmannsbergerDivision of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.
Neil E MartinDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.ORCID 0000-0002-8164-8516
Kathryn NevelDivision of Medical Oncology, Indiana University School of Medicine, Indianapolis, IN, United States.ORCID 0000-0003-1499-837X
John KincaidDepartment of Neurology, Indiana University, Indianapolis, IN, United States.
Lawrence H EinhornDivision of Medical Oncology, Indiana University School of Medicine, Indianapolis, IN, United States.ORCID 0000-0001-7971-7669
Lois B TravisDivision of Medical Oncology, Indiana University School of Medicine, Indianapolis, IN, United States.ORCID 0000-0002-6010-3541

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI FRANCESCA M GANY · 1985 to 2026
$347.4M
Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Reuben Kapur · 1999 to 2026
$59.3M
Genetic Susceptibility and Biomarkers of Platinum-related ToxicitiesR01CA157823 · NCI · UNIVERSITY OF ROCHESTER · PI TRAVIS, LOIS B. · 2012 to 2025
$11.2M
Risk Prediction for Development of Adverse Effects FOllowing Radiotherapy for Prostate CancerK07CA187546 · NCI · UNIVERSITY OF ROCHESTER · PI KERNS, SARAH L. · 2015 to 2019
$649k
NCI NIH HHS 2R01 CA157823NCI NIH HHS K07 CA187546NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA082709NCI NIH HHS R01 CA157823NIH HHS
6 · The paper itself

Abstract

backgroundTo comprehensively evaluate the longitudinal progression of cumulative burden of morbidity (CBM) in testicular cancer survivors (TCS) following standard-dose cisplatin-based chemotherapy and the impact of modifiable risk factors on morbidity and early mortality.

methodsParticipants completed first-line chemotherapy at or longer than 6 months before baseline assessments with comprehensive questionnaires and physical examinations. Based on follow-up assessments (median: 7 years later), longitudinal progression of adverse health outcomes (AHOs) and CBM score (encompassing AHO number and severity) were examined. Baseline health behaviors and AHOs were evaluated for associations with mortality using mixed-effects parametric proportional-hazards regression to identify modifiable risk factors.

resultsAmong 616 TCS longitudinally assessed, 23% experienced worsening CBM postchemotherapy (median = 11 years, interquartile range = 7-15). Declines were driven by worsening treatment-related AHOs: tinnitus (29.7%), hearing loss (24.4%), Raynaud's disease (22.6%), neuropathy (18.5%), and neuropathic pain (10.7%). Baseline factors associated with worsening neuropathy included lack of aerobic physical activity (odds ratio [OR] = 1.98, 95% confidence interval [CI] = 1.06 to 3.72), and obesity (OR = 1.85, 95% CI = 1.17 to 2.92). These were also related to worsening neuropathic pain (OR = 2.82, P = .009 and OR = 2.29, P = .023). Twenty-nine deaths occurred among 1830 5-year TCS (4.2% cumulative hazard) (median age = 48 years, range = 22-74). Participants reporting neuropathic pain (hazard ratio [HR] = 3.64, 95% CI = 1.45 to 9.10), no aerobic (HR = 6.56, 95% CI = 2.73 to 15.8), or no low-impact physical activity (HR = 3.96, 95% CI = 1.40 to 11.2) had significantly higher mortality, as did TCS indicating fair (HR = 9.23, 95% CI = 3.08 to 27.8) or poor (HR = 18.5, 95% CI = 3.30 to 103) health. Relationships between pain and mortality were mediated through lowered physical activity (P = .036).

conclusionsClinically actionable factors associated with early mortality identify high-risk TCS in need of closer monitoring and targeted interventions. The significant relationship between neuropathic pain and mortality, mediated by low physical activity, is the first to our knowledge in TCS.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCisplatinTesticular NeoplasmsAdultCancer SurvivorsDisease ProgressionHumansLongitudinal StudiesMaleMiddle AgedMorbidityRisk FactorsYoung AdultCisplatin

Identifiers

PMID39898813
PMCPMC12415966

What Socratic holds

Textmetadata
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Registered trials

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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 Socratic graph.