Fatigue in breast cancer patients on chemotherapy: a cross-sectional study exploring clinical, biological, and genetic factors

BMC Cancer. 2022 Jan 3;22(1):16. doi: 10.1186/s12885-021-09072-0.

Abstract

Background: Cancer-related fatigue (CRF) is one of the most common and distressing complaints reported by cancer patients during chemotherapy considerably impacting all aspects of a patient's life (physical, psychosocial, professional, and socioeconomic). The aim of this study was to assess the severity of cancer-related fatigue in a group of breast cancer patients undergoing chemotherapy and explore the association between fatigue scores and sociodemographic, clinical, biological, psychiatric, and genetic factors.

Methods: A cross-sectional pilot study carried out at the oncology outpatient unit of Hôtel-Dieu de France University Hospital recruited 67 breast cancer patients undergoing chemotherapy between November 2017 and June 2019 to evaluate fatigue using the EORTC QLQ-C30 scale (European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire). Genotyping for seven gene polymorphisms (COMT, DRD2, OPRM1, CLOCK, PER2, CRY2, ABCB1) was performed using the Lightcycler® (Roche).

Results: The prevalence of fatigue was 46.3%. Multivariable analysis taking the fatigue score as the dependent variable showed that a higher number of cycles and a lower hemoglobin level were significantly associated with higher odds of exhibiting fatigue. Moreover, having at least one C allele for DRD2 SNP (vs. TT) was significantly associated with a 4.09 higher odds of expressing fatigue compared to TT patients. Finally, patients with at least one C allele for CLOCK SNP tended to display higher fatigue levels than TT patients.

Conclusions: Our study showed that anemic breast cancer patients with a high number of chemotherapy cycles and those carrying at least one C allele for DRD2 and CLOCK SNPs are at greater risk of exhibiting fatigue. Since no previous research has reported such genetic results, future studies are necessary to confirm our findings.

Keywords: Breast cancer; CLOCK; Chemotherapy; DRD2; Fatigue; Pharmacogenetics.

MeSH terms

  • Aged
  • Alleles
  • Anemia / chemically induced
  • Anemia / genetics
  • Antineoplastic Agents / adverse effects*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / psychology
  • CLOCK Proteins / genetics
  • Cross-Sectional Studies
  • Fatigue / chemically induced*
  • Fatigue / genetics*
  • Female
  • France
  • Humans
  • Middle Aged
  • Pharmacogenomic Variants / genetics
  • Pilot Projects
  • Polymorphism, Single Nucleotide
  • Quality of Life
  • Receptors, Dopamine D2 / genetics
  • Surveys and Questionnaires

Substances

  • Antineoplastic Agents
  • DRD2 protein, human
  • Receptors, Dopamine D2
  • CLOCK Proteins
  • CLOCK protein, human