Impact of cancer related fatigue on quality of life of 1,262 patients with breast cancer receiving chemotherapy: A URCC NCORP nationwide phase III RCT.

J Jeremy McGuire (University of Rochester Medical Center, Rochester, NY) N Nikesha Gilmore J Joseph John Guido (University of Rochester Medical Center Department of Neurobiology and Anatomy, Rochester, NY) C Chin-Shang Li (Department of Surgery, Division of Supportive Care in Cancer and URCC NCORP Research Base, University of Rochester Medical Center, Rochester, NY) K Kevin Spath (University of Rochester Medical Center, Rochester, NY) J Jeffrey Ramos-Santiago B Belal Firwana (Heartland Cancer Research NCORP, St Louis, MO) T Thomas James Saphner (Aurora Health, Two Rivers, WI) S Samer Kasbari (Southeast Clinical Oncology Research Consortium, Goldsboro, NC) L Luke Joseph Peppone (University of Rochester Medical Center, Rochester, NY)

Abstract

12130 Background: Cancer-related fatigue (CRF) is one of the most common and debilitating symptoms reported by cancer patients, significantly impairing quality of life (QoL) across physical, functional, emotional, and social domains. Despite its prevalence, limited data exist quantifying how rapid changes in CRF after a single chemotherapy cycle influence QoL. We aim to evaluate if rapid clinically meaningful changes in CRF post chemotherapy impact QoL in breast cancer patients. Methods: This Phase III RCT (NCT03367572) enrolled chemotherapy-naïve breast cancer patients across 21 NCORP practices receiving high/moderate emetogenic chemotherapy. CRF was assessed at baseline and post chemotherapy cycle 1 (n = 1,262) using a four-day home diary, with maximum fatigue change as the primary outcome. For analysis, the CRF variable was dichotomized into two categories: a clinically significant increase (≥3 points) and less than a 3-point increase. QOL was measured with FACT-G and its subscales: emotional (EWB), functional (FWB), physical (PWB), and social (SWB). ANCOVA and Cohen’s d effect size (ES) evaluated whether clinically meaningful CRF changes predicted QOL changes across cycles. Results: Among 1,262 patients with valid fatigue scores, 74.8% experienced increased CRF after cycle 1, with 53.2% reporting a ≥3-point increase and a mean increase of 2.9 points for the group. Clinically significant increases in CRF strongly impacted quality of life (QOL), as reflected in FACT-G Total Score changes post-cycle 1 (≥3: −12.4 vs < 3: −4.7; mean difference: 7.7, p < 0.001, ES: 0.74), exceeding the clinically meaningful threshold of > 5 points. Analysis of the subscales revealed PWB with the largest changes of 4.8 (≥3: −X vs < 3: −X; p < 0.001, ES: 1.00). FWB changes were 2.1 (≥3: −X vs < 3: −X; p≤0.0001, ES: 0.48) and EWB changes were 0.7 (≥3: −X vs < 3: −X; p < 0.001, ES: 0.26). CRF did not significantly impact SWB. Notably, many of these subscale changes surpassed the clinically meaningful threshold of > 2 points. Conclusions: This study underscores the rapid onset and significant impact of CRF on QoL in breast cancer patients receiving chemotherapy. Clinically meaningful increases in CRF, even after a single chemotherapy cycle, were predictive of substantial declines in QoL, particularly in physical and functional well-being. These results emphasize the urgent need for targeted fatigue management strategies, such as tailored interventions addressing physical and functional domains, to improve patient outcomes. Clinical trial information: NCT03367572 .

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 12130-12130
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

J

Jeremy McGuire

University of Rochester Medical Center, Rochester, NY

N

Nikesha Gilmore

J

Joseph John Guido

University of Rochester Medical Center Department of Neurobiology and Anatomy, Rochester, NY

C

Chin-Shang Li

Department of Surgery, Division of Supportive Care in Cancer and URCC NCORP Research Base, University of Rochester Medical Center, Rochester, NY

K

Kevin Spath

University of Rochester Medical Center, Rochester, NY

J

Jeffrey Ramos-Santiago

B

Belal Firwana

Heartland Cancer Research NCORP, St Louis, MO

T

Thomas James Saphner

Aurora Health, Two Rivers, WI

S

Samer Kasbari

Southeast Clinical Oncology Research Consortium, Goldsboro, NC

L

Luke Joseph Peppone

University of Rochester Medical Center, Rochester, NY