<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(5)</volume><submitter>Lee SE</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>We investigated the feasibility of the clinical application of non-invasive transthoracic echocardiography for diagnosis of pulmonary arterial hypertension induced by dasatinib (D-PAH) in chronic myeloid leukemia (CML).&lt;h4>Methods&lt;/h4>A total of 451 CML patients who were examined by 2D-echocardiography at least once at baseline and/or during dasatinib therapy as frontline (n = 196) and subsequent line (n = 255) therapies were included in this study. D-PAH was defined as right ventricular systolic pressure (RVSP) >40 mm Hg with relevant symptoms and the absence of other specific etiologies.&lt;h4>Results&lt;/h4>A total of 847 echocardiographies were performed including at baseline (n = 255) and during dasatinib treatment (n = 592). During the median of 36.2 (0.1-181.8) months o</pubmed_abstract><journal>Cancer medicine</journal><pagination>1515-1524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7940235</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Change of right ventricular systolic pressure can indicate dasatinib-induced pulmonary arterial hypertension in chronic myeloid leukemia.</pubmed_title><pmcid>PMC7940235</pmcid><pubmed_authors>Kim DW</pubmed_authors><pubmed_authors>Kim SH</pubmed_authors><pubmed_authors>Youn HJ</pubmed_authors><pubmed_authors>Jang EJ</pubmed_authors><pubmed_authors>Lee SE</pubmed_authors><pubmed_authors>Jung HE</pubmed_authors><pubmed_authors>Chung WB</pubmed_authors><pubmed_authors>Chung NG</pubmed_authors><pubmed_authors>Joong Oh S</pubmed_authors><pubmed_authors>Cho B</pubmed_authors><pubmed_authors>Hyun Kong J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Change of right ventricular systolic pressure can indicate dasatinib-induced pulmonary arterial hypertension in chronic myeloid leukemia.</name><description>&lt;h4>Background&lt;/h4>We investigated the feasibility of the clinical application of non-invasive transthoracic echocardiography for diagnosis of pulmonary arterial hypertension induced by dasatinib (D-PAH) in chronic myeloid leukemia (CML).&lt;h4>Methods&lt;/h4>A total of 451 CML patients who were examined by 2D-echocardiography at least once at baseline and/or during dasatinib therapy as frontline (n = 196) and subsequent line (n = 255) therapies were included in this study. D-PAH was defined as right ventricular systolic pressure (RVSP) >40 mm Hg with relevant symptoms and the absence of other specific etiologies.&lt;h4>Results&lt;/h4>A total of 847 echocardiographies were performed including at baseline (n = 255) and during dasatinib treatment (n = 592). During the median of 36.2 (0.1-181.8) months o</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-05T13:50:56.175Z</modification><creation>2025-04-05T13:50:56.175Z</creation></dates><accession>S-EPMC7940235</accession><cross_references><pubmed>33590711</pubmed><doi>10.1002/cam4.3588</doi></cross_references></HashMap>