Usefulness of patient-reported outcomes to assess the effectiveness of topical hormonal therapy for gynecologic symptoms after antihormonal treatment for breast cancer.

Atrophic vaginitis breast cancer patient-reported outcomes topical estrogen

Journal

Proceedings (Baylor University. Medical Center)
ISSN: 0899-8280
Titre abrégé: Proc (Bayl Univ Med Cent)
Pays: United States
ID NLM: 9302033

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 13 12 2019
revised: 24 02 2020
accepted: 06 03 2020
entrez: 18 7 2020
pubmed: 18 7 2020
medline: 18 7 2020
Statut: epublish

Résumé

The aim of this retrospective study was to assess the efficacy of topical hormonal therapy (THT) to relieve vaginal symptoms resulting from antihormonal therapy in women with hormone receptor-positive breast cancer. A total of 74 breast cancer patients who received THT for vaginal complaints were retrospectively identified and statistically matched with 74 control breast cancer patients with vaginal complaints with no documented use of THT. Symptom scores were recorded from the center's proprietary patient-reported outcomes database, Patient Care Monitor (ConcertoHealthAI, Boston). A baseline score was noted at the initiation of antihormonal therapy and was followed at 6 and 12 months. The median differences between baseline, 6-month, and 12-month scores were analyzed. Repeated measures analysis of variance assessed the impact of topical hormonal replacement. There was no statistically significant difference in score change between the two groups at 6 and 12 months. In the active THT group, there were no statistically significant differences in vaginal complaints or sexual problems over time: {

Identifiants

pubmed: 32675948
doi: 10.1080/08998280.2020.1744059
pii: 1744059
pmc: PMC7340418
doi:

Types de publication

Journal Article

Langues

eng

Pagination

331-335

Informations de copyright

Copyright © 2020 Baylor University Medical Center.

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Auteurs

Amit L Jain (AL)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Omer Jamy (O)

Department of Hematology Oncology, University of Alabama Birmingham School of MedicineBirminghamAlabama.

Janice Mullins (J)

Medical Oncology, West Cancer Center and Research InstituteMemphisTennessee.

Rana Muhammad Usman (RM)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Felicia Hare (F)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Poojitha Valasareddy (P)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Amina Chaudhry (A)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Julie Ryder (J)

Medical Oncology, West Cancer Center and Research InstituteMemphisTennessee.

Justin R Smith (JR)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Emily Miller (E)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Harsha Ranganath (H)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.

Lee Schwartzberg (L)

Medical Oncology, West Cancer Center and Research InstituteMemphisTennessee.

Edward Stepanski (E)

Vector OncologyMemphisTennessee.

Mark Walker (M)

Vector OncologyMemphisTennessee.

Justin Gatwood (J)

Department of Clinical Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee.

Gregory A Vidal (GA)

Department of Internal Medicine, Division of Hematology Oncology, University of Tennessee Health Sciences CenterMemphisTennessee.
Medical Oncology, West Cancer Center and Research InstituteMemphisTennessee.

Classifications MeSH