Abstract
Purpose
Ensuring there are clear standards for addressing cancer-related sexual side effects is important. Currently, there are differences in two leading sets of clinical guidelines regarding the inclusion of survivors’ romantic partners into clinical discussions between survivors and their providers about this issue. To help refine guidelines, we examine breast cancer survivor, partner, and oncology provider perspectives about including partners in discussions about cancer-related sexual side effects in a secondary analysis of a broader qualitative study.
Methods
Partnered female breast cancer survivors (N = 29) completed online surveys, and intimate partners of breast cancer survivors (N = 12) and breast oncology providers (N = 8) completed semi-structured interviews. Themes were derived from thematic content analysis.
Results
Among survivors who reported a discussion with their provider, fewer than half indicated their partner had been present, despite most survivors expressing it was — or would have been — helpful to include their partner. Partners also largely indicated being included was or would have been helpful, when welcomed by the survivor. Providers similarly emphasized the importance of survivors’ autonomy in deciding whether to discuss sexual concerns in the presence of a partner.
Conclusions
Partners were infrequently included in conversations about cancer-related sexual side effects, even though survivors, partners, and providers alike expressed value in these discussions occurring with the couple together — when that is the survivor’s preference. Findings suggest future clinical guidelines should emphasize that incorporating partners into clinical discussions about sexual concerns is important for many breast cancer patients. Soliciting and enacting patients’ preferences is essential for truly patient-centered care.
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Data availability
Data available upon reasonable request from the authors.
Code availability
N/A.
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Acknowledgements
Authors are sincerely grateful for the participation of the survivors, partners, and providers in this study, for the support of the UVA Breast Care Center, and for the recruitment assistance of Dora Irvin, LPN.
Funding
This study was funded by a University of Virginia (UVA) Cancer Center, Cancer Control and Population Sciences (CCPH) health program, and Population Research Pilot Projects award. Dr. Shaffer was supported in part by the National Institutes of Health (NIH) and National Center for Advancing Translational Sciences (NCATS) award numbers UL1TR003015 and KL2TR003016. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
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KS, conceptualization, methodology, data curation, formal analysis, resources, writing—original draft, writing—review and editing, funding acquisition; EK, methodology, investigation, data curation, formal analysis, writing—review and editing, project administration; JG, data curation, formal analysis, writing—review and editing, project administration; AC, methodology resources, writing—review and editing, supervision, funding acquisition; WC, conceptualization, methodology, resources, writing—review and editing, supervision, funding acquisition; JBR, conceptualization, writing—review and editing; TM, conceptualization, writing—review and editing; KI, conceptualization, writing—review and editing; LR, resources, writing—review and editing, supervision, funding acquisition; SS, conceptualization, methodology, resources, writing—review and editing, supervision, funding acquisition.
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This study was approved as exempt research by the Institutional Review Board at the University of Virginia.
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Shaffer, K.M., Kennedy, E., Glazer, J.V. et al. Including partners in discussions of sexual side effects from breast cancer: a qualitative study of survivors, partners, and providers. Support Care Cancer 30, 4935–4944 (2022). https://doi.org/10.1007/s00520-022-06917-7
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DOI: https://doi.org/10.1007/s00520-022-06917-7