Abstract
Purpose
To compare the impact of exercise and mind–body prehabilitation interventions on changes in quality of life and cancer treatment-related symptoms in women with newly diagnosed breast cancer.
Methods
The following describes a secondary analysis of a randomized window of opportunity trial (The Pre-Operative Health and Body Study). Forty-nine women were randomized to participate in either an exercise prehabilitation intervention or a mind–body prehabilitation intervention from the time of enrollment to surgery. Participants (N = 47) completed measures of quality of life, anxiety, depression, and stress at the time of enrollment (T1), post-intervention/surgery (T2), and one-month post-surgery (T3). Changes in outcome measures between groups were compared over time using longitudinal models.
Results
Mind–body group participants experienced significant improvements in cognitive functioning in comparison to exercise group participants between T1 and T3 (difference in average change: -9.61, p = 0.04, d = 0.31), otherwise, there were no significant differences between groups. Within group comparisons demonstrated that both groups experienced improvements in anxiety (exercise: average change = -1.18, p = 0.03, d = 0.34; mind–body: average change = -1.69, p = 0.006, d = 0.43) and stress (exercise: average change = -2.33, p = 0.04, d = 0.30; mind–body: average change = -2.59, p = 0.05, d = 0.29), while mind–body group participants experienced improvements in insomnia (average change = -10.03, p = 0.04, d = 0.30) and cognitive functioning (average change = 13.16, p = 0.0003, d = 0.67).
Conclusions
Both prehabilitation interventions impacted cancer treatment-related symptoms. Further work in larger groups of patients is needed to evaluate the efficacy of prehabilitation interventions on quality of life in women with breast cancer. Pre-operative exercise and mind–body interventions may impact physical and/or psychological effects of cancer diagnosis and treatment in women with breast cancer.
Trial registration
ClinicalTrials.gov Identifier: NCT01516190. Registered January 24, 2012.
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Data availability
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
The authors would like to acknowledge Laura Shockro and Nancy Campbell for their assistance with data collection and implementation of the study interventions.
Funding
Funding was provided by the Susan G. Komen Foundation (in collaboration with the Society for Women's Health Research) and the American Institute for Cancer Research. Susan G. Komen Foundation (Society for Women's Health): SPSWHR1001 (principal investigator: J.A. Ligibel, co-principal investigator: M.L. Irwin; to J.A. Ligibel, M.L. Irwin, N. Campbell, D. Dillon, and A. Giobbie-Hurder); American Institute for Cancer Research (no grant number; principal investigator: J.A. Ligibel; to J.A. Ligibel, D. Dillon, N. Campbell, and A. Giobbie-Hurder).
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All authors contributed to the study conception and design of the primary study and/or secondary analysis. Data analysis was performed by Anita Giobbie-Hurder. The first draft of the manuscript was written by Robert Knoerl and all authors provided feedback on subsequent versions. All authors read and approved the final manuscript.
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This study was performed in line with the principles of the Declaration of Helsinki. Approval was granted by the Dana-Farber/Harvard Cancer Center Office for Human Research Studies (Protocol: 11–182; 7/14/2011).
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Informed consent was obtained from all individual participants included in the study.
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Conflict of interest
SMT has served as a paid adviser/consultant for AstraZeneca, Lilly, Merck, Nektar, Novartis, Pfizer, Eisai, NanoString, Puma, Immunomedics, Genentech/Roche, Bristol Myers Squibb, Sanofi, Paxman, Seattle Genetics, Athenex, and Celldex; and has received research funding from AstraZeneca, Lilly, Merck, Nektar, Novartis, Pfizer, Eisai, Genentech/Roche, Exelixis, Immunomedics, Cyclacel, and Bristol Myers Squibb. DD is on the Advisory Board of Oncology Analytics and consults for Novartis. EW has received personal fees (consulting) from Athenex, Carrick Therapeutics, G1 Therapeutics, Genentech/Roche, Genomic Health, GSK, Jounce, Leap, Lilly, Novartis, Seattle Genetics, Syros, and Zymeworks; has received research funding from Astra Zeneca and Genentech/Roche; and serves on the scientific advisory board of Leap. RK has received personal fees (consulting) from Strategy Inc, Spark Healthcare, and System Analytic; and serves on the scientific advisory board of Wellium.
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Knoerl, R., Giobbie-Hurder, A., Sannes, T.S. et al. Exploring the impact of exercise and mind–body prehabilitation interventions on physical and psychological outcomes in women undergoing breast cancer surgery. Support Care Cancer 30, 2027–2036 (2022). https://doi.org/10.1007/s00520-021-06617-8
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DOI: https://doi.org/10.1007/s00520-021-06617-8