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Psychological Distress,Anxiety, and Depression of Cancer-Affected BRCA1/2 Mutation Carriers: a Systematic Review
Authors:Johanna?Ringwald  author-information"  >  author-information__contact u-icon-before"  >  mailto:johanna.ringwald@med.uni-tuebingen.de"   title="  johanna.ringwald@med.uni-tuebingen.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Christina?Wochnowski,Kristin?Bosse,Katrin?Elisabeth?Giel,Norbert?Sch?ffeler,Stephan?Zipfel,Martin?Teufel
Affiliation:1.Department of Psychosomatic Medicine and Psychotherapy, Internal Medicine VI,University Hospital Tuebingen,Tuebingen,Germany;2.Comprehensive Cancer Center,University Hospital Tuebingen,Tuebingen,Germany;3.Institute of Medical Genetics and Applied Genomics,University Hospital Tuebingen,Tuebingen,Germany;4.Department of Obstetrics and Gynecology,University Hospital Tuebingen,Tuebingen,Germany
Abstract:Understanding the intermediate- and long-term psychological consequences of genetic testing for cancer patients has led to encouraging research, but a clear consensus of the psychosocial impact and clinical routine for cancer-affected BRCA1 and BRCA2 mutation carriers is still missing. We performed a systematic review of intermediate- and long-term studies investigating the psychological impact like psychological distress, anxiety, and depression in cancer-affected BRCA mutation carriers compared to unaffected mutation carriers. This review included the screening of 1243 studies. Eight intermediate- and long-term studies focusing on distress, anxiety, and depression symptoms among cancer-affected mutation carriers at least six months after the disclosure of genetic testing results were included. Studies reported a great variety of designs, methods, and patient outcomes. We found evidence indicating that cancer-affected mutation carriers experienced a negative effect in relation to psychological well-being in terms of an increase in symptoms of distress, anxiety, and depression in the first months after test disclosure. In the intermediate- and long-term, no significant clinical relevant symptoms occurred. However, none of the included studies used specific measurements, which can clearly identify psychological burdens of cancer-affected mutation carriers. We concluded that current well-implemented distress screening instruments are not sufficient for precisely identifying the psychological burden of genetic testing. Therefore, future studies should implement coping strategies, specific personality structures, the impact of genetic testing, supportive care needs and disease management behaviour to clearly screen for the possible intermediate- and long-term psychological impact of a positive test disclosure.
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