<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Graf SA</submitter><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>176-181</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7904587</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Histologic transformation to diffuse large B-cell lymphoma (tDLBCL) occurs in a significant proportion of indolent lymphomas. However, few studies of novel agents inform its management, particularly when relapsed after or refractory (R/R) to prior treatment.&lt;h4>Patients and methods&lt;/h4>We prospectively evaluated ibrutinib monotherapy in pathologically documented patients with R/R tDLBCL in a single-arm study. The primary endpoint was overall response rate.&lt;h4>Results&lt;/h4>Twenty patients who had received a median of 4 (range, 2-9) prior lines of therapy overall (median, 2.5; range, 1-9 for tDLBCL) were treated. The overall response rate was 35%, including complete responses in 15%. The median progression-free survival and overall survival were 4.1 months (95% confidence i</pubmed_abstract><journal>Clinical lymphoma, myeloma &amp; leukemia</journal><pubmed_title>Ibrutinib Monotherapy in Relapsed or Refractory, Transformed Diffuse Large B-cell Lymphoma.</pubmed_title><pmcid>PMC7904587</pmcid><funding_grant_id>P30 CA015704</funding_grant_id><funding_grant_id>K24 CA184039</funding_grant_id><pubmed_authors>Krakow E</pubmed_authors><pubmed_authors>Smith SD</pubmed_authors><pubmed_authors>Lynch RC</pubmed_authors><pubmed_authors>Kanan S</pubmed_authors><pubmed_authors>Soma L</pubmed_authors><pubmed_authors>Behnia S</pubmed_authors><pubmed_authors>Rasmussen H</pubmed_authors><pubmed_authors>Chauncey TR</pubmed_authors><pubmed_authors>Voutsinas JM</pubmed_authors><pubmed_authors>Graf SA</pubmed_authors><pubmed_authors>Wu QV</pubmed_authors><pubmed_authors>Morris K</pubmed_authors><pubmed_authors>Gopal AK</pubmed_authors><pubmed_authors>Cassaday RD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ibrutinib Monotherapy in Relapsed or Refractory, Transformed Diffuse Large B-cell Lymphoma.</name><description>&lt;h4>Background&lt;/h4>Histologic transformation to diffuse large B-cell lymphoma (tDLBCL) occurs in a significant proportion of indolent lymphomas. However, few studies of novel agents inform its management, particularly when relapsed after or refractory (R/R) to prior treatment.&lt;h4>Patients and methods&lt;/h4>We prospectively evaluated ibrutinib monotherapy in pathologically documented patients with R/R tDLBCL in a single-arm study. The primary endpoint was overall response rate.&lt;h4>Results&lt;/h4>Twenty patients who had received a median of 4 (range, 2-9) prior lines of therapy overall (median, 2.5; range, 1-9 for tDLBCL) were treated. The overall response rate was 35%, including complete responses in 15%. The median progression-free survival and overall survival were 4.1 months (95% confidence i</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-05-18T12:36:35.745Z</modification><creation>2025-04-05T10:03:54.415Z</creation></dates><accession>S-EPMC7904587</accession><cross_references><pubmed>33358575</pubmed><doi>10.1016/j.clml.2020.11.023</doi></cross_references></HashMap>