期刊
CURRENT GENETIC MEDICINE REPORTS
卷 9, 期 4, 页码 59-69出版社
SPRINGERNATURE
DOI: 10.1007/s40142-021-00201-6
关键词
Cancer risk; Transgender; Genetics; Personalised care
资金
- Cancer Research UK through the CanGene-CanVar research programme
- NHS Central and South GMSA
- NHS Wales
- Cancer Research UK
- Pfizer Genomics
Based on the research mentioned above, tailored risk assessments and management recommendations need to be provided for transgender patients, multidisciplinary teams should be established to make shared decisions with patients, and national guidelines are required to standardize discussions on risk-reducing options and screening.
Purpose of Review To best support all patients with inherited cancer risk, we must broaden our scope of practice to consider the needs of the transgender and gender diverse (trans) community. We considered best practice for supporting trans patients including tailored risk assessments and management recommendations. Recent Findings There is limited literature considering trans patient care in cancer genetics. Small case studies have highlighted how medical transition and cancer risk-reducing options intersect with the need for individualised care. Studies have also shown that cancer genetics professionals do not feel prepared to support trans patients. Patient-centred care for trans patients relies on a multidisciplinary team (MDT) engaged in shared decision-making. National guidelines are needed to standardise access to appropriate discussions around risk-reducing options and screening. International collaborative research is required to provide empiric data on the impact of gender-affirming treatments on cancer risk, and more experiential data is needed from trans patients accessing cancer genetics services. Finally, education and training in this area should be formally embedded for all cancer genetics professionals.
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