<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jagadeesh D</submitter><funding>National Institute of Arthritis and Musculoskeletal and Skin Diseases</funding><funding>Patient Education and Research Fund</funding><funding>Seagen Inc</funding><funding>Anderson Cancer Center Core</funding><funding>Takeda Pharmaceutical Company Ltd</funding><funding>Cutaneous T-Cell Lymphoma</funding><funding>National Cancer Institute</funding><funding>Haas Family Foundation</funding><funding>NCI NIH HHS</funding><funding>Millennium Pharmaceuticals Inc</funding><pagination>864-873</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9526494</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(10)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The safety and efficacy of brentuximab vedotin (BV), an antibody-drug conjugate directed to the CD30 antigen, has been assessed in several trials in patients with peripheral T-cell lymphoma (PTCL), cutaneous T-cell lymphoma (CTCL), or B-cell non-Hodgkin lymphoma (NHL). The objective of this research was to examine the relationship between CD30 expression level and clinical response to BV.&lt;h4>Patients and methods&lt;/h4>We analyzed response in patients treated with BV monotherapy in 5 prospective clinical studies in relapsed or refractory PTCL, CTCL, or B-cell NHL. CD30 expression was assessed by immunohistochemistry (IHC) using the Ber H2 antibody for 275 patients.&lt;h4>Results&lt;/h4>Across all 5 studies, 140 (50.9%) patients had tumors with CD30 expression &lt;10%, including 60 (</pubmed_abstract><journal>The oncologist</journal><pubmed_title>Response to Brentuximab Vedotin by CD30 Expression in Non-Hodgkin Lymphoma.</pubmed_title><pmcid>PMC9526494</pmcid><funding_grant_id>R21-CA74117</funding_grant_id><funding_grant_id>K24 CA 86815</funding_grant_id><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>SGN35-IST-002</funding_grant_id><funding_grant_id>SGN35-IST-030</funding_grant_id><funding_grant_id>K24 CA086815</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>CA16672-22</funding_grant_id><funding_grant_id>SGN35-IST-r001</funding_grant_id><pubmed_authors>Horwitz S</pubmed_authors><pubmed_authors>Duvic M</pubmed_authors><pubmed_authors>Onsum M</pubmed_authors><pubmed_authors>Lisano J</pubmed_authors><pubmed_authors>Bartlett NL</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Advani R</pubmed_authors><pubmed_authors>Jagadeesh D</pubmed_authors><pubmed_authors>Little M</pubmed_authors><pubmed_authors>Fenton K</pubmed_authors><pubmed_authors>Jacobsen E</pubmed_authors><pubmed_authors>Trepicchio W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Response to Brentuximab Vedotin by CD30 Expression in Non-Hodgkin Lymphoma.</name><description>&lt;h4>Background&lt;/h4>The safety and efficacy of brentuximab vedotin (BV), an antibody-drug conjugate directed to the CD30 antigen, has been assessed in several trials in patients with peripheral T-cell lymphoma (PTCL), cutaneous T-cell lymphoma (CTCL), or B-cell non-Hodgkin lymphoma (NHL). The objective of this research was to examine the relationship between CD30 expression level and clinical response to BV.&lt;h4>Patients and methods&lt;/h4>We analyzed response in patients treated with BV monotherapy in 5 prospective clinical studies in relapsed or refractory PTCL, CTCL, or B-cell NHL. CD30 expression was assessed by immunohistochemistry (IHC) using the Ber H2 antibody for 275 patients.&lt;h4>Results&lt;/h4>Across all 5 studies, 140 (50.9%) patients had tumors with CD30 expression &lt;10%, including 60 (</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-07-14T17:10:49.242Z</modification><creation>2025-04-05T17:26:06.51Z</creation></dates><accession>S-EPMC9526494</accession><cross_references><pubmed>35948003</pubmed><doi>10.1093/oncolo/oyac137</doi></cross_references></HashMap>