Fatigue and quality of life during neoadjuvant chemotherapy of early breast cancer: a prospective multicenter cohort study
- PMID: 37966690
- PMCID: PMC10764505
- DOI: 10.1007/s12282-023-01520-y
Fatigue and quality of life during neoadjuvant chemotherapy of early breast cancer: a prospective multicenter cohort study
Abstract
Background: Few measurements of fatigue and quality of life have been performed during neoadjuvant chemotherapy of early breast cancer. This study evaluates fatigue and quality of life experienced by early breast cancer patients during neoadjuvant chemotherapy and their association with different clinical parameters.
Methods: Fifty-four stage I-III patients' responses to the Multidimensional Fatigue Inventory (MFI) and to the Functional Assessment of Cancer Therapy-Breast (FACT-B) were analyzed by a linear covariance pattern model. Chemotherapy regimen, age, baseline fatigue level, body-mass-index and cancer stage were added to the model to estimate their impact on both outcomes.
Results: All fatigue dimensions worsened in clinically relevant levels. Physical fatigue worsened the most, mental fatigue the least. For quality of life, physical and functional well-being worsened the most. Only emotional well-being improved during chemotherapy. Physical well-being worsened more during standard than during dose-dense chemotherapy, and more during anthracycline than during taxane cycles. Age, body-mass-index and cancer stage had no impact. The higher the fatigue levels at baseline, the less they worsened during chemotherapy.
Conclusions: Further actions to reduce fatigue and improve quality of life during neoadjuvant chemotherapy of early breast cancer are needed. Focus should be laid on the physical dimension. Future research should also investigate the impact of different chemotherapy sequences and densities on fatigue and quality of life.
Study registration: The study was registered in the German Clinical Trials Register in May 2019 (DRKS00016761).
Keywords: Breast cancer; Cancer-related fatigue; Cohort study; Neoadjuvant chemotherapy; Quality of life.
© 2023. The Author(s).
Conflict of interest statement
The nonprofit organizations Society for Cancer Research and Gesellschaft für klinische Forschung e.V. are minority shareholders of Iscador AG, a manufacturer of mistletoe extracts, which are being used for supportive care in oncology. No products of Iscador AG were investigated in the current study. FP, WT, MR, SS and SB are or have been employed by Iscador AG during at least some part of the study. MK has received remuneration from Springer Press, Biermann Press, Celgene, AstraZeneca, Myriad Genetics, TEVA, Eli Lilly GSK, Seagen, received consultancy or advisory fees from Myriad Genetics, Bavarian KVB, DKMS Life, BLÄK, TEVA and exeltis, holds stock in Therawis Diagnostics GmbH and AIM GmbH and received funding from Sphingotec, Deutsche Krebshilfe, DFG, BMBF, Bavarian State Ministry of Economy, Innovation Fond GBA, the Senator Roesner Foundation and the Dr Pommer-Jung Foundation. TK has received honoraria from Merck Sharp & Dohme, Astra Zeneca, Pfizer, Gilead, Daiichi Sankyo, Endomag, Sirius medical, Hologic, Merit Medical and received support for attending meetings from Daiichi Sankyo. DP received honoraria from Seagen, Gilead, Iscador AG, Kneipp Ärztebund and holds an unpaid leadership role in the AGO Kommission Integrative Medizin. CM, DDM, IUB have no conflict of interest.
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