Hematocrit Is Associated with Cancer-Related Fatigue in Colorectal Cancer Survivors: A Longitudinal Analysis

Author:

Kiebach Joann1ORCID,de Vries-ten Have Judith12ORCID,van Duijnhoven Fränzel J.B.1ORCID,Kok Dieuwertje E.1ORCID,van Lanen Anne-Sophie1ORCID,Kouwenhoven Ewout A.3ORCID,de Wilt Johannes H.W.4ORCID,Schrauwen Ruud W.M.5ORCID,Kampman Ellen1ORCID,Winkels Renate M.1ORCID,Wesselink Evertine1ORCID

Affiliation:

1. 1Division of Human Nutrition and Health, Wageningen University & Research, Wageningen, the Netherlands.

2. 2Consumption and Healthy Lifestyles Chair group, Wageningen University & Research, Wageningen, the Netherlands.

3. 3Department of Surgery, Hospital Group Twente ZGT, Almelo, the Netherlands.

4. 4Department of Surgery, Radboud University Medical Center, Nijmegen, the Netherlands.

5. 5Department of Gastroenterology and Hepatology, Bernhoven, Uden, the Netherlands.

Abstract

Abstract Background: Cancer-related fatigue (CRF) is a frequent symptom in colorectal cancer survivors. It is unknown to what extent anemia may contribute to CRF in colorectal cancer survivors. This study aimed to investigate the association between hematocrit, as marker for anemia, and CRF among colorectal cancer survivors from diagnosis until two years thereafter. Methods: The study population included 1,506 newly diagnosed colorectal cancer survivors at any stage of disease from a prospective cohort study. Hematocrit and CRF (EORTC QLQ-C30) were assessed at diagnosis, six months, and two years after diagnosis. Multivariable logistic regression or multivariable linear mixed models were used to assess the associations of hematocrit with CRF prevalence, or CRF severity over time, respectively. Results: A low hematocrit (levels <40% men/<36% women) was present in a third of the survivors at diagnosis and six months thereafter, and among 16% two years after diagnosis. The prevalence of CRF was 15% at diagnosis, peaked at 27% at six months, and was 14% two years after diagnosis. Hematocrit was associated with the prevalence of CRF at diagnosis [OR, 0.92; confidence interval (CI), 0.88–0.95], 6 months (OR, 0.89; 95% CI, 0.86–0.92), and 2 years (OR, 0.91; CI, 0.87–0.96) after diagnosis. Lower hematocrit was associated with higher severity of CRF over time (beta-coefficient = 1.3; CI, 1.5–1.1). Conclusions: Lower hematocrit levels were longitudinally associated with a higher prevalence and severity of CRF in colorectal cancer. Impact: Our findings emphasize the importance of long-term anemia monitoring and a potential role of anemia in CRF among colorectal cancer survivors.

Funder

World Cancer Research Fund International

KWF Kankerbestrijding

Publisher

American Association for Cancer Research (AACR)

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