<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>29(4)</volume><submitter>Hayashi S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>In 2018, BRACAnalysis® was covered by medical insurance in Japan as a companion diagnostic test for the poly ADP-ribose polymerase inhibitor olaparib. In April 2020, eligibility for BRCA1/2 genetic testing was expanded to the diagnosis of hereditary breast and ovarian cancer syndrome, and medical management including prophylactic surgery and surveillance were covered by public insurance for BRCA1/2 mutation carriers who developed breast or ovarian cancer. The amount of BRCA1/2 genetic testing has been increasing recently, but the number of subjects and the impact of testing for patients' outcomes remain unclear.&lt;h4>Patients and methods&lt;/h4>This study explored the potential number of patients who will be eligible for new insurance coverage for BRCA1/2 genetic testing. We </pubmed_abstract><journal>Breast cancer (Tokyo, Japan)</journal><pagination>659-665</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9225975</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genetic medicine is accelerating in Japan.</pubmed_title><pmcid>PMC9225975</pmcid><pubmed_authors>Nakamura M</pubmed_authors><pubmed_authors>Morisaki T</pubmed_authors><pubmed_authors>Takao Y</pubmed_authors><pubmed_authors>Hayashi S</pubmed_authors><pubmed_authors>Kaneshiro K</pubmed_authors><pubmed_authors>Shimazaki A</pubmed_authors><pubmed_authors>Yamada M</pubmed_authors><pubmed_authors>Kubo M</pubmed_authors><pubmed_authors>Kai M</pubmed_authors><pubmed_authors>Shikada S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic medicine is accelerating in Japan.</name><description>&lt;h4>Background&lt;/h4>In 2018, BRACAnalysis® was covered by medical insurance in Japan as a companion diagnostic test for the poly ADP-ribose polymerase inhibitor olaparib. In April 2020, eligibility for BRCA1/2 genetic testing was expanded to the diagnosis of hereditary breast and ovarian cancer syndrome, and medical management including prophylactic surgery and surveillance were covered by public insurance for BRCA1/2 mutation carriers who developed breast or ovarian cancer. The amount of BRCA1/2 genetic testing has been increasing recently, but the number of subjects and the impact of testing for patients' outcomes remain unclear.&lt;h4>Patients and methods&lt;/h4>This study explored the potential number of patients who will be eligible for new insurance coverage for BRCA1/2 genetic testing. We </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-05-29T19:01:57.841Z</modification><creation>2024-10-19T08:37:14.59Z</creation></dates><accession>S-EPMC9225975</accession><cross_references><pubmed>35191009</pubmed><doi>10.1007/s12282-022-01342-4</doi></cross_references></HashMap>