<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>73</volume><submitter>Chang L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Rosai-Dorfman disease (RDD) is a rare heterogeneous histiocytic disorder lacking standardized first-line treatment.&lt;h4>Methods&lt;/h4>This single-center, phase 2 prospective study enrolled 13 newly diagnosed and 10 recurrent RDD patients from June 2021 to March 2023 at Peking Union Medical College Hospital (Beijing, China). Lenalidomide 25 mg days 1-21 plus dexamethasone 40 mg days 1, 8, 15, 22 was administered in 28-day cycles, totaling 12 cycles. The primary endpoint was progression-free survival (PFS). Secondary endpoints were overall response rate (ORR) to lenalidomide and dexamethasone (RD) regimen, toxicity, and overall survival (OS) measured from RD start to death or last follow-up. OS and PFS were estimated according to Kaplan-Meier survival analysis and compared wi</pubmed_abstract><journal>EClinicalMedicine</journal><pagination>102685</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11253284</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lenalidomide and dexamethasone for Rosai-Dorfman disease: a single arm, single center, prospective phase 2 study.</pubmed_title><pmcid>PMC11253284</pmcid><pubmed_authors>Zhou DB</pubmed_authors><pubmed_authors>Lang M</pubmed_authors><pubmed_authors>Cao XX</pubmed_authors><pubmed_authors>Chang L</pubmed_authors><pubmed_authors>Liu ZZ</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Cai H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lenalidomide and dexamethasone for Rosai-Dorfman disease: a single arm, single center, prospective phase 2 study.</name><description>&lt;h4>Background&lt;/h4>Rosai-Dorfman disease (RDD) is a rare heterogeneous histiocytic disorder lacking standardized first-line treatment.&lt;h4>Methods&lt;/h4>This single-center, phase 2 prospective study enrolled 13 newly diagnosed and 10 recurrent RDD patients from June 2021 to March 2023 at Peking Union Medical College Hospital (Beijing, China). Lenalidomide 25 mg days 1-21 plus dexamethasone 40 mg days 1, 8, 15, 22 was administered in 28-day cycles, totaling 12 cycles. The primary endpoint was progression-free survival (PFS). Secondary endpoints were overall response rate (ORR) to lenalidomide and dexamethasone (RD) regimen, toxicity, and overall survival (OS) measured from RD start to death or last follow-up. OS and PFS were estimated according to Kaplan-Meier survival analysis and compared wi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-02T11:51:39.15Z</modification><creation>2025-04-06T17:10:41.752Z</creation></dates><accession>S-EPMC11253284</accession><cross_references><pubmed>39022796</pubmed><doi>10.1016/j.eclinm.2024.102685</doi></cross_references></HashMap>