Evidence map›Paper›PMID 42611514›Full record

ArticleJAMA network open2026

Long-Term Fatigue After Treatment for Breast Cancer.

Nancy E Avis, Nathaniel S O'Connell, Shannon L Mihalko, Jennifer H Jordan, Amy C Ladd, Glenn J Lesser, Kristine C Olson, Kathryn E Weaver, Emily V Dressler, Pamela J Grizzard and 17 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02791581 (Understanding and Predicting Breast Cancer Events After Treatment), which is not on this 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.

NCT02791581 naactive not recruitingnot on this map

Understanding and Predicting Breast Cancer Events After Treatment (UPBEAT)

TypeinterventionalSponsorWake Forest University Health SciencesRan2017 to 2034Enrolled403ConditionsBreast CancerArmsCardiac MRI
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

27 authors.

Nancy E AvisDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, North Carolina.
Nathaniel S O'ConnellDepartment of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Shannon L MihalkoDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, North Carolina.
Jennifer H JordanVCU Pauley Heart Center, Division of Cardiology at Virginia Commonwealth University, Richmond.
Amy C LaddVCU Pauley Heart Center, Division of Cardiology at Virginia Commonwealth University, Richmond.
Glenn J LesserDepartment of Cancer Medicine at Wake Forest School of Medicine, Winston-Salem, North Carolina.
Kristine C OlsonVCU Pauley Heart Center, Division of Cardiology at Virginia Commonwealth University, Richmond.
Kathryn E WeaverDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, North Carolina.
Emily V DresslerDepartment of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Pamela J GrizzardVCU Pauley Heart Center, Division of Cardiology at Virginia Commonwealth University, Richmond.
Beverly LevineDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, North Carolina.
Tonya L MooreSection on Cardiovascular Medicine, Department of Internal Medicine at Wake Forest School of Medicine, Winston-Salem, North Carolina.
Bonnie KyDepartment of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Mary Helen HackneyDepartment of Hematology, Oncology, and Palliative Care, Massey Cancer Center, Virginia Commonwealth University, Richmond.
Peter BrubakerDepartment of Health and Exercise Science, Wake Forest University, Winston-Salem, North Carolina.
Kerryn W RedingUniversity of Washington School of Nursing, University of Washington, Seattle.
Alexander R LucasDepartment of Social and Behavioral Sciences, Virginia Commonwealth University School of Public Health, Richmond.
Moriah P BellissimoVCU Pauley Heart Center, Division of Cardiology at Virginia Commonwealth University, Richmond.
F Gerard MoellerDepartment of Psychiatry, Virginia Commonwealth University, Richmond.
Dalane W KitzmanSection on Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Craig A HamiltonBiomedical Engineering, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Heidi D KlepinDepartment of Cancer Medicine at Wake Forest School of Medicine, Winston-Salem, North Carolina.
Joseph YeboahSection on Cardiovascular Medicine, Department of Internal Medicine at Wake Forest School of Medicine, Winston-Salem, North Carolina.
William NtimUniversity of North Carolina School of Medicine, Novant Health Campus, Novant Heart and Vascular Institute, Charlotte.
Vlad G ZahaHarold CSimmons Comprehensive Cancer Center, Dallas, Texas; Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Ralph D'AgostinoDepartment of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
W Gregory HundleyVCU Pauley Heart Center, Division of Cardiology at Virginia Commonwealth University, Richmond.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Patients with breast cancer (BC) may have long-term fatigue after treatment, which is associated with reduced quality of life. Objective: To identify cardiac, psychological, and cancer treatment factors associated with fatigue before and 24 months after BC treatment. Design, Setting, and Participants: This cohort study was conducted across multiple community hospital-based cancer centers among participants with stage I to III BC receiving potentially cardiotoxic chemotherapy or aromatase inhibitors and noncancer comparators. Participants were enrolled from May 2017 to July 2021 and followed up for 24 months. Data were analyzed between July 2023 and July 2026. Exposures: Fatigue was assessed by the Functional Assessment of Chronic Illness Therapy Fatigue scale. Main Outcomes and Measures: It was hypothesized that chemotherapy-associated changes in left ventricular function were associated with and mediated 2-year post-BC treatment fatigue. Outcome measures included fatigue, sociodemographic variables, hematocrit, left ventricular ejection fraction and circumferential strain, cardiovascular comorbidities, 6-minute walk distance, perceived stress, and depressive symptoms. Results: From a total of 381 patients, patients with BC (236) and noncancer comparators (145) had a mean (SD) age of 54 (12) years. Two years after BC treatment, 33 (18.2%) receiving potentially cardiotoxic chemotherapy experienced clinically relevant fatigue (χ2 test P < .001 relative to aromatase inhibitors or controls), and 62 (34.6%) experienced a significant increase in fatigue relative to their precancer treatment fatigue level (χ2 test P < .001, relative to aromatase inhibitors and controls). Independent of pretreatment and posttreatment left ventricular ejection fraction, diabetes status, hypertension, tobacco use, age, body mass index, hematocrit, receipt of potentially cardioprotective medications, and chemotherapy regimens, only depressive symptoms (estimate, -0.77; 95% CI, -0.83 to -0.71; P < .001) and perceived stress (-0.32; 95% CI, -0.41 to -0.24; P < .001) were associated with and mediated 24-month post-BC treatment fatigue measures. Baseline adjusted changes in 6-minute walk distance, left ventricular ejection fraction, and left ventricular strain were not associated with 24-month post-BC treatment fatigue levels. Conclusions and Relevance: In this cohort study of patients with BC, clinically relevant fatigue increased in 34% of patients 2 years after initiating cancer treatment mediated partly by depressive symptoms and perceived stress regardless of cardiovascular risk factors, age, or change in left ventricular ejection fraction and/or strain. Trial Registration: ClinicalTrials.gov Identifier: NCT02791581.

Indexed as

Antineoplastic AgentsBreast NeoplasmsFatigueAromatase InhibitorsCohort StudiesFemaleHumansMiddle AgedQuality of LifeAntineoplastic AgentsAromatase Inhibitors

Identifiers

PMID42611514
PMCPMC13487558

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Registered trials

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.