Multimodal, Technology-Assisted Intervention for the Management of Menopause after Cancer Improves Cancer-Related Quality of Life—Results from the Menopause after Cancer (Mac) Study

Author:

Donohoe Fionán1ORCID,O’Meara Yvonne1,Roberts Aidin1,Comerford Louise1,Valcheva Ivaila1ORCID,Kearns Una2,Galligan Marie3,Higgins Michaela J.4ORCID,Henry Alasdair L.56,Kelly Catherine M.7,Walshe Janice M.4ORCID,Hickey Martha8,Brennan Donal J.19ORCID

Affiliation:

1. UCD Gynaecological Oncology Group, UCD School of Medicine, Mater Misericordiae University Hospital, Eccles Street, D07 AX57 Dublin, Ireland

2. myPatientSpace Ltd., K36 A022 Dublin, Ireland

3. Clinical Research Centre, UCD School of Medicine, Mater Misericordiae University Hospital, Eccles Street, D07 AX57 Dublin, Ireland

4. Department of Medical Oncology, St. Vincent’s University Hospital, Elm Park, D04 T6F4 Dublin, Ireland

5. Big Health Ltd., London WC1H 9LT, UK

6. Big Health Ltd., San Francisco, CA 94108, USA

7. Department of Medical Oncology, Mater Misericordiae University Hospital, Eccles Street, D07 AX57 Dublin, Ireland

8. Department of Obstetrics and Gynaecology, University of Melbourne and The Royal Women’s Hospital, Parkville, VIC 3052, Australia

9. Systems Biology Ireland, UCD School of Medicine, Belfield, D04 V1W8 Dublin, Ireland

Abstract

Background: Vasomotor symptoms (VMSs) associated with menopause represent a significant challenge for many patients after cancer treatment, particularly if conventional menopausal hormone therapy (MHT) is contraindicated. Methods: The Menopause after Cancer (MAC) Study (NCT04766229) was a single-arm phase II trial examining the impact of a composite intervention consisting of (1) the use of non-hormonal pharmacotherapy to manage VMS, (2) digital cognitive behavioral therapy for insomnia (dCBT-I) using Sleepio (Big Health), (3) self-management strategies for VMS delivered via the myPatientSpace mobile application and (4) nomination of an additional support person/partner on quality of life (QoL) in women with moderate-to-severe VMS after cancer. The primary outcome was a change in cancer-specific global QoL assessed by the EORTC QLC C-30 v3 at 6 months. Secondary outcomes included the frequency of VMS, the bother/interference of VMS and insomnia symptoms. Results: In total, 204 women (82% previous breast cancer) with a median age of 49 years (range 28–66) were recruited. A total of 120 women completed the protocol. Global QoL scores increased from 62.2 (95%CI 58.6–65.4) to 70.4 (95%CI 67.1–73.8) at 6 months (p < 0.001) in the intention to treatment (ITT) cohort (n = 204) and from 62 (95%CI 58.6–65.4) to 70.4 (95%CI 67.1–73.8) at 6 months (p < 0.001) in the per-protocol (PP) cohort (n = 120). At least 50% reductions were noticed in the frequency of VMS as well as the degree of bother/interference of VMS at six months. The prevalence of insomnia reduced from 93.1% at the baseline to 45.2% at 6 months (p < 0.001). The Sleep Condition Indicator increased from 8.5 (SEM 0.4) to 17.3 (SEM 0.5) (p < 0.0005) in the ITT cohort and 7.9 (SEM 0.4) to 17.3 (SEM 0.5) (p < 0.001) in the PP cohort. Conclusions: A targeted composite intervention improves the quality of life for cancer patients with frequent and bothersome vasomotor symptoms with additional benefits on frequency, the bother/interference of VMS and insomnia symptoms.

Funder

Irish Cancer Society

Publisher

MDPI AG

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