The interest and knowledge of genetic counseling and genetic testing for hereditary breast cancer in a community hospital

• Published in: JOURNAL OF FAMILIAL TUMORS Vol. 19; no. 2; pp. 66 - 71
• Main Authors: Minohata, Junya, Kono, Seishi, Matsumoto, Hitomi, Nishigami, Takashi
• Format: Journal Article
• Language: Japanese
• Published: The Japanese Society for Hereditary Tumors 2019; 一般社団法人日本遺伝性腫瘍学会
• Subjects: hereditary breast cancer, genetic testing, breast cancer, recognition about the heredity; 遺伝性乳癌，遺伝学的検査，乳癌患者，認識
• ISSN: 1346-1052; 2189-6674
• DOI: 10.18976/jsft.19.2_66

This study investigated interest and knowledge of genetic counseling and testing for hereditary breast and ovarian cancer syndrome among breast cancer patients in our hospital which is one of the community hospitals without established department of medical genetics.We performed questionnaire surveys and direct interviews by a clinical nurse specialist in cancer care. The surveys and interviews were administered to 22 breast cancer patients who visited the hospital between March 1 and May 31, 2017 and met the criteria for further genetic risk evaluation in NCCN guidelines (version 2.2016). Although 21(95%) and 18(82%) patients knew the words of “hereditary breast cancer” and “genetic test” respectively, only 7(32%) knew “genetic counseling”. Both the questionnaire and direct interview revealed that patients who had strong interest in hereditary breast cancer did not always wish to receive genetic testing. Nineteen(86%) patients answered that a high cost could be a reason to hesitate to undergo genetic testing in the questionnaire surveys, as confirmed by the direct interviews. In conclusion, even community hospitals urgently need to establish a system for patients’ accessing to the correct information on hereditary cancer and genetic counseling.