Evidence map›Paper›PMID 39028321›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2024

The impact of non- and anthracycline-based chemotherapy on fatigue in breast cancer survivors: results from WF-97415.

Nancy E Avis, Beverly J Levine, Heidi D Klepin, Shannon L Mihalko, Peter H Brubaker, Tonya Moore, Amy C Ladd, Susan F Dent, Mary Helen Hackney, Bonnie Ky and 5 more

Abstract readMulticenter Study
In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2024. 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. Article
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

15 authors.

Nancy E AvisDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC, 27157, USA. navis@wakehealth.edu.ORCID http://orcid.org/0000-0002-1077-3037
Beverly J LevineDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC, 27157, USA.
Heidi D KlepinDepartment of Hematology and Oncology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Shannon L MihalkoDepartment of Health and Exercise Science, Wake Forest University, Winston-Salem, NC, USA.
Peter H BrubakerDepartment of Health and Exercise Science, Wake Forest University, Winston-Salem, NC, USA.
Tonya MooreSection On Cardiovascular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Amy C LaddDepartment of Internal Medicine, Division of Cardiology, Pauley Heart Center, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Susan F DentDivision of Medical Oncology, Duke Cancer Institute, Duke University, Durham, NC, USA.
Mary Helen HackneyDepartment of Hematology, Oncology, and Palliative Care, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Bonnie KyDivision of Cardiovascular Medicine, University of Pennsylvania, Philadelphia, PA, USA.
William O NtimUNC School of Medicine, Novant Health Campus, Novant Heart & Vascular Institute, Charlotte, NC, USA.
Lynne I WagnerUNC Gillings School of Global Public Health, UNC Lineberger Comprehensive Cancer Center, Chapel Hill, NC, USA.
Kathryn E WeaverDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC, 27157, USA.
W Gregory HundleyDepartment of Internal Medicine, Division of Cardiology, Pauley Heart Center, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
UPBEAT study team

Funding

ECOG-ACRIN NCORP Research Base - TMISTUG1CA189828 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$199.7M
Wake Forest NCORP Research BaseUG1CA189824 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Emily Van Meter Dressler, GLENN J LESSER · 2014 to 2026
$57.9M
Understanding and Predicting Fatigue, CV Decline & Events After Breast CA TreatmentR01CA199167 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HUNDLEY, WILLIAM GREGORY · 2015 to 2022
$3.2M
NCI NIH HHS R01CA199167NCI NIH HHS UG1 CA189824NCI NIH HHS UG1CA189824NCI NIH HHS UG1 CA189828NCI NIH HHS UG1CA189828
6 · The paper itself

Abstract

purposeTo examine the differential effect of non- and anthracycline-based chemotherapy on fatigue over 12 months post-diagnosis among breast cancer survivors.

methodsThis study is based on a prospective Wake Forest NCI Community Oncology Research Program (NCORP) multicenter cohort study (WF-97415) of women with stage I to III breast cancer and non-cancer controls. Analyses compared those: 1) receiving, or 2) not receiving anthracycline chemotherapy, 3) receiving aromatase inhibitors (AIs) without chemotherapy, with 4) a comparator group without a history of cancer. In-person clinic assessments were conducted at: baseline (prior to chemotherapy or start of AI therapy), and 3 and 12 months after baseline. The Functional Assessment of Chronic Illness Therapy-Fatigue scale was the primary outcome. Estimated least squares means by group using mixed models with a random subject effect, fixed effects of time and group, and the interaction between time and group was used to compare groups across time, controlling for age, comorbidities, and treatment variables.

resultsAmong 284 women (mean age = 53.4 years, sd 11.9 years), there was a significant (p < 0.0001) group by time interaction, with a sharp increase in fatigue at 3 months in the two chemotherapy groups in comparison to the non-chemotherapy and non-cancer controls. The two chemotherapy groups did not significantly differ in fatigue at any time point.

conclusionWomen with breast cancer who receive non- or anthracycline-based chemotherapy experience similar trends in and levels of fatigue within the first year of treatment and greater fatigue than women receiving AIs alone or women without breast cancer.

Indexed as

AnthracyclinesBreast NeoplasmsCancer SurvivorsFatigueAdultAgedAntineoplastic AgentsAromatase InhibitorsCohort StudiesFemaleHumansMiddle AgedProspective StudiesAnthracyclinesAntineoplastic AgentsAromatase InhibitorsAnthracyclineBreast neoplasmChemotherapyFatigueLongitudinal

Identifiers

PMID39028321
PMCPMC11271320

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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 OpenQuestion graph.