{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,16]],"date-time":"2026-07-16T10:10:35Z","timestamp":1784196635569,"version":"3.55.0"},"reference-count":43,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2026,6,4]],"date-time":"2026-06-04T00:00:00Z","timestamp":1780531200000},"content-version":"vor","delay-in-days":3,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"},{"start":{"date-parts":[[2026,6,1]],"date-time":"2026-06-01T00:00:00Z","timestamp":1780272000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100010101","name":"Taichung Veterans General Hospital","doi-asserted-by":"publisher","award":["TCVGH\u20101133701D"],"award-info":[{"award-number":["TCVGH\u20101133701D"]}],"id":[{"id":"10.13039\/501100010101","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100010101","name":"Taichung Veterans General Hospital","doi-asserted-by":"publisher","award":["TCVGH\u20101140701D"],"award-info":[{"award-number":["TCVGH\u20101140701D"]}],"id":[{"id":"10.13039\/501100010101","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100010101","name":"Taichung Veterans General Hospital","doi-asserted-by":"publisher","award":["TCVGH\u2010YM1140115"],"award-info":[{"award-number":["TCVGH\u2010YM1140115"]}],"id":[{"id":"10.13039\/501100010101","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Cancer Medicine"],"published-print":{"date-parts":[[2026,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Therapy for chronic lymphocytic leukemia (CLL) has shifted from chemoimmunotherapy to targeted agents such as Bruton's tyrosine kinase (BTK) inhibitors and BCL\u20102 inhibitors. Approved first\u2010line options include acalabrutinib, a second\u2010generation BTK inhibitor, and the fixed\u2010duration combination venetoclax\u2013obinutuzumab, yet real\u2010world head\u2010to\u2010head data are scarce.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Using the TriNetX global federated health database, we retrospectively compared outcomes in treatment\u2010na\u00efve patients with TP53\u2010unmutated CLL who received either regimen as initial therapy. After applying eligibility criteria and 1:1 propensity score matching, 669 matched pairs were analyzed. The primary endpoint was time to next treatment (TTNT); secondary endpoints included overall survival (OS) and adverse events.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The results showed that patients treated with venetoclax plus obinutuzumab had a significantly longer\n                      <jats:styled-content style=\"fixed-case\">TTNT<\/jats:styled-content>\n                      (median not reached vs. 47.7\u2009months) and improved 4\u2010year\n                      <jats:styled-content style=\"fixed-case\">OS<\/jats:styled-content>\n                      . Across all subgroups, the venetoclax\u2010based regimen performed better. Cytopenias and infections were more common with venetoclax\u2013obinutuzumab\u2014neutropenia 54.3% versus 33.3%, thrombocytopenia 45.9% versus 31.9%, febrile neutropenia 7.1% versus 3.4%, and tumor lysis syndrome 6.3% versus 2.3%. Acalabrutinib caused fewer severe hematologic toxicities.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>In real\u2010world practice, venetoclax plus obinutuzumab was associated with longer TTNT and improved OS compared to acalabrutinib as first\u2010line therapy in patients with TP53 wild\u2010type CLL.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/cam4.72022","type":"journal-article","created":{"date-parts":[[2026,6,5]],"date-time":"2026-06-05T05:15:38Z","timestamp":1780636538000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Acalabrutinib Versus Venetoclax Plus Obinutuzumab in Treatment\u2010Naive Chronic Lymphocytic Leukemia: A Real\u2010World Propensity Score\u2010Matched Study"],"prefix":"10.1002","volume":"15","author":[{"given":"Po\u2010Wei","family":"Liao","sequence":"first","affiliation":[{"name":"Division of Hematology\/Medical Oncology, Department of Medicine Taichung Veterans General Hospital  Taichung Taiwan"},{"name":"Department of Life Science Tunghai University  Taichung Taiwan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bor\u2010Sheng","family":"Ko","sequence":"additional","affiliation":[{"name":"School of Medicine, National Taiwan University College of Medicine  Taipei Taiwan"},{"name":"Department of Hematological Oncology National Taiwan University Cancer Center  Taipei City Taiwan"},{"name":"Division of Hematology, Department of Internal Medicine National Taiwan University Hospital  Taipei City Taiwan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yu\u2010Chen","family":"Su","sequence":"additional","affiliation":[{"name":"Division of Hematology\/Medical Oncology, Department of Medicine Taichung 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