Health professionals’ evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer

Springer Science and Business Media LLC - Tập 14 - Trang 265-272 - 2014
Kirsten F. L. Douma1, Bettina Meiser2, Judy Kirk3, Gillian Mitchell4,5, Christobel Saunders6, Belinda Rahman2, Mariana S. Sousa2, Kristine Barlow-Stewart7, Margaret Gleeson8, Kathy Tucker9
1Department of Medical Psychology, Academic Medical Center/University of Amsterdam, Amsterdam, The Netherlands.
2Psychosocial Research Group, Lowy Cancer Research Centre C25, Prince of Wales Clinical School, University of New South Wales Australia, Sydney, Australia
3Familial Cancer Service, Westmead Institute for Cancer Research, Westmead Millenium Institute, University of Sydney, Sydney, Australia
4Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Australia
5Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia
6School of Surgery, University of Western Australia, Crawley, Australia
7Sydney Medical School, Sydney University, Sydney, Australia
8Hunter Family Cancer Service, Newcastle, Australia
9Hereditary Cancer Clinic, Prince of Wales Hospital, Randwick, Sydney, Australia

Tóm tắt

Increasingly, women are offered genetic testing shortly after diagnosis of breast cancer to facilitate decision-making about treatment, often referred to as ‘treatment-focused genetic testing’ (TFGT). As understanding the attitudes of health professionals is likely to inform its integration into clinical care we surveyed professionals who participated in our TFGT randomized control study. Thirty-six completed surveys were received (response rate 59 %), 15 (42 %) health professionals classified as genetic and 21 (58 %) as non-genetic. Mainly positive experiences with participating in the TFGT trial were reported. The high cost of testing and who could best deliver information about TGFT to the patient were raised as key constraints to implementation of TFGT in usual care. More non-genetic than genetic health professionals (44 vs 8 %) preferred that the surgeon provide the information for decision-making about TFGT. While costs of TFGT itself and the time and effort of staff involved were perceived barriers, as testing costs become lower, it is expected that TFGT will become a routine part of standard clinical care for patients at high genetic risk in the near future.

Tài liệu tham khảo

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