<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(6)</volume><submitter>Yang H</submitter><pubmed_abstract>The non-germinal center B-cell like (non-GCB) subtype of diffuse large B-cell lymphoma (DLBCL) has poor clinical outcomes. Bruton tyrosine kinase (BTK) inhibitors have established therapeutic activity in B-cell malignancies, with modest activity in DLBCL. Zanubrutinib, a potent and selective BTK inhibitor, was evaluated in patients with relapsed or refractory (R/R) non-GCB DLBCL. The BGB-3111-207 study (NCT03145064) was a multicenter single-arm phase 2 study. Patients received twice-daily oral zanubrutinib, 160 mg, until disease progression or unacceptable toxicity. The primary end point was the overall response rate (ORR). Secondary end points included progression-free survival (PFS) and duration of response (DOR). Overall survival (OS) was an exploratory end point. Forty-one patients wer</pubmed_abstract><journal>Blood advances</journal><pagination>1629-1636</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8941452</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Zanubrutinib monotherapy for relapsed or refractory non-germinal center diffuse large B-cell lymphoma.</pubmed_title><pmcid>PMC8941452</pmcid><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Guo W</pubmed_authors><pubmed_authors>Novotny W</pubmed_authors><pubmed_authors>Zhao W</pubmed_authors><pubmed_authors>Zou D</pubmed_authors><pubmed_authors>Xiang B</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Lv F</pubmed_authors><pubmed_authors>Tan Z</pubmed_authors><pubmed_authors>Guo H</pubmed_authors><pubmed_authors>Liu A</pubmed_authors><pubmed_authors>Fu L</pubmed_authors><pubmed_authors>Song Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Zanubrutinib monotherapy for relapsed or refractory non-germinal center diffuse large B-cell lymphoma.</name><description>The non-germinal center B-cell like (non-GCB) subtype of diffuse large B-cell lymphoma (DLBCL) has poor clinical outcomes. Bruton tyrosine kinase (BTK) inhibitors have established therapeutic activity in B-cell malignancies, with modest activity in DLBCL. Zanubrutinib, a potent and selective BTK inhibitor, was evaluated in patients with relapsed or refractory (R/R) non-GCB DLBCL. The BGB-3111-207 study (NCT03145064) was a multicenter single-arm phase 2 study. Patients received twice-daily oral zanubrutinib, 160 mg, until disease progression or unacceptable toxicity. The primary end point was the overall response rate (ORR). Secondary end points included progression-free survival (PFS) and duration of response (DOR). Overall survival (OS) was an exploratory end point. Forty-one patients wer</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-10T01:38:13.961Z</modification><creation>2025-02-19T01:11:53.492Z</creation></dates><accession>S-EPMC8941452</accession><cross_references><pubmed>34638136</pubmed><doi>10.1182/bloodadvances.2020003698</doi></cross_references></HashMap>