Associations between Menopausal Hormone Therapy and Colorectal, Lung, or Melanoma Cancer Recurrence and Mortality: A Narrative Review.
Gabriel FiolIñaki LeteLaura NietoAna SantaballaMaría Jesús PlaLaura BaquedanoJoaquín CalafPluvio CoronadoEsther de la ViudaPlácido LlanezaBorja OteroSonia Sánchez-MéndezIsabel RamírezNicolas Mendozanull nullPublished in: Journal of clinical medicine (2023)
Objective: to develop eligibility criteria for use in non-gynecological cancer patients. Methods: We searched all the articles published in peer-reviewed journals up to March 2021. We utilized the PICOS standards and the following selection criteria: menopausal women with a history of non-gynecological and non-breast cancer who underwent hormone replacement therapy (HRT) using various preparations (oestrogens alone or in combination with a progestogen, tibolone, or tissue selective oestrogen complex) and different routes of administration (including oral, transdermal, vaginal, or intra-nasal). We focused on randomized controlled trials as well as relevant extension studies or follow-up reports, specifically examining recurrence and mortality outcomes. Results: Women colorectal cancer survivors who use MHT have a lower risk of death from any cause than those survivors who do not use MHT. Women who are skin melanoma survivors using MHT have a longer survival rate than non-MHT survivors. There is no evidence that women lung cancer survivors who use MHT have a different survival rate than those who do not use MHT. Conclusions: MHT is safe for women who have a history of colorectal, lung, or skin melanoma cancers.
Keyphrases
- polycystic ovary syndrome
- young adults
- replacement therapy
- pregnancy outcomes
- free survival
- breast cancer risk
- cervical cancer screening
- randomized controlled trial
- childhood cancer
- cardiovascular events
- clinical trial
- cardiovascular disease
- systematic review
- type diabetes
- insulin resistance
- smoking cessation
- papillary thyroid
- pregnant women
- coronary artery disease
- adipose tissue
- mesenchymal stem cells
- adverse drug
- chronic rhinosinusitis
- lymph node metastasis
- drug induced
- double blind