Abstract
Purpose
Data are lacking about the association between quality of life (QOL) and psychosocial issues of partners of young women with breast cancer who co-parent dependent children.
Methods
We conducted a cross-sectional analysis of partners of women with breast cancer diagnosed at age ≤ 40. Among those partners reporting at least one dependent child under 18 years old at the time of diagnosis, we used multiple linear regression to examine associations between partner QOL and sociodemographic and psychosocial factors, and the patient’s cancer stage and time since diagnosis.
Results
Of the 219 parenting partners, all identified as male with a median age of 44 years; 96% (204/213) reported working full-time at the time of the survey. Fifty-four percent endorsed behaviors indicating maladaptive coping. In adjusted analyses, less than full-time employment (β = − 8.76; 95% CI = − 17.37, − 0.14), younger age (β = − 0.35; 95% CI = − 0.069, − 0.02), greater parenting concerns (β = 0.56; 95% CI = 0.36, 0.75), clinically relevant anxiety symptoms (β = 13.79; 95% CI = 10.24, 17.35), lower post-traumatic growth score (β = − 0.33; 95% CI = − 0.51, − 0.16), lower social support (β = − 0.21; 95% CI = − 0.29, − 0.12), lower sexual satisfaction (β = − 0.40; 95% CI = − 0.62, − 0.19), and breast cancer stages 3 (β = 7.61; 95% CI = 0.19, 15.02) and 4 (β = 12.63; 95% CI = 1.91, 23.34), when compared to stage 0, were associated with lower partner QOL.
Conclusion
Parenting partners of young women with breast cancer have substantial unmet psychosocial needs. Interventions are needed to enhance QOL and promote adaptive coping for this population.
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Data availability
The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
Code availability
The primary authors have full control of all codes and agree to allow the journal to review the codes if requested.
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Funding
Susan G. Komen (AHP); Breast Cancer Research Foundation (AHP); The Pink Agenda (AHP).
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N.A.B. provided the initial conceptualization for and writing of the original draft of the manuscript. A.H.P. provided funding acquisition for this study. N.A.B., T.F.G., S.M.R., S.G., Y.Z., and A.H.P. had a significant contribution to the conceptualization of the cohort, methodology, acquisition of the data investigation, analysis, and manuscript writing. M.M. provided project management for the study and contributed to data acquisition. K.J.R., L.S., S.C., V.B., T.C., P.M. contributed to review and editing. N.A.B., T.F.G., and A.H.P. were responsible for the final manuscript edits.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional review board committee (IRB) and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was approved by IRBs of the Dana-Farber Harvard Cancer Center, Simmons University, and 12 other participating sites (Beth Israel Deaconess Medical Center, Brigham and Women’s Hospital, Cape Cod Hospital, Faulkner Hospital, Lowell General Hospital, Massachusetts General Hospital, Mayo Clinic, Newton-Wellesley Hospital, North Shore Cancer Center Salem, South Shore Hospital, Sunnybrook Health Sciences Centre, and University of Colorado Hospital).
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Nancy A. Borstelmann and Tamryn F. Gray are co-first authors for this article.
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Borstelmann, N.A., Gray, T.F., Gelber, S. et al. Psychosocial issues and quality of life of parenting partners of young women with breast cancer. Support Care Cancer 30, 4265–4274 (2022). https://doi.org/10.1007/s00520-022-06852-7
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DOI: https://doi.org/10.1007/s00520-022-06852-7