<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Penack O</submitter><funding>National Institute for Health Research (NIHR)</funding><pagination>380-386</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10920188</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>59(3)</volume><pubmed_abstract>Ruxolitinib has become the new standard of care for steroid-refractory and steroid-dependent chronic GVHD (SR-cGVHD). Our aim was to collect comparative data between ruxolitinib and extracorporeal photophoresis (ECP). We asked EBMT centers if they were willing to provide detailed information on GVHD grading, -therapy, -dosing, -response and complications for each included patient. 31 centers responded positively and we included all patients between 1/2017-7/2019 treated with ECP or ruxolitinib for moderate or severe SR-cGVHD. We identified 84 and 57 patients with ECP and ruxolitinib, respectively. We performed multivariate analyses adjusted on grading and type of SR-cGVHD (steroid dependent vs. refractory vs. intolerant to steroids). At day+180 after initiation of treatment for SR-cGVHD the odds ratio in the ruxolitinib group to achieve overall response vs. the ECP group was 1.35 (95% CI = [0.64; 2.91], p = 0.43). In line, we detected no statistically significant differences in overall survival, progression-free survival, non-relapse mortality and relapse incidence. The clinical significance is limited by the retrospective study design and the current data can't replace prospective studies on ECP in SR-cGVHD. However, the present results contribute to the accumulating evidence on ECP as an effective treatment option in SR-cGVHD.</pubmed_abstract><journal>Bone marrow transplantation</journal><pubmed_title>ECP versus ruxolitinib in steroid-refractory chronic GVHD - a retrospective study by the EBMT transplant complications working party.</pubmed_title><pmcid>PMC10920188</pmcid><funding_grant_id>CL-2015-09-001</funding_grant_id><pubmed_authors>Wichert S</pubmed_authors><pubmed_authors>Kornblit BT</pubmed_authors><pubmed_authors>Kinsella F</pubmed_authors><pubmed_authors>Holderried TAW</pubmed_authors><pubmed_authors>Chiusolo P</pubmed_authors><pubmed_authors>Ozdogu H</pubmed_authors><pubmed_authors>Boreland W</pubmed_authors><pubmed_authors>Gavriilaki E</pubmed_authors><pubmed_authors>Daguenet E</pubmed_authors><pubmed_authors>Moiseev I</pubmed_authors><pubmed_authors>Penack O</pubmed_authors><pubmed_authors>Peric Z</pubmed_authors><pubmed_authors>Afanasyeva K</pubmed_authors><pubmed_authors>Schoemans H</pubmed_authors><pubmed_authors>Reinhardt HC</pubmed_authors><pubmed_authors>Peczynski C</pubmed_authors><pubmed_authors>Avenoso D</pubmed_authors><pubmed_authors>Piekarska A</pubmed_authors><pubmed_authors>Lemaitre J</pubmed_authors><pubmed_authors>Martinez C</pubmed_authors><pubmed_authors>Koenecke C</pubmed_authors><pubmed_authors>Mico MC</pubmed_authors><pubmed_authors>Basak GW</pubmed_authors></additional><is_claimable>false</is_claimable><name>ECP versus ruxolitinib in steroid-refractory chronic GVHD - a retrospective study by the EBMT transplant complications working party.</name><description>Ruxolitinib has become the new standard of care for steroid-refractory and steroid-dependent chronic GVHD (SR-cGVHD). Our aim was to collect comparative data between ruxolitinib and extracorporeal photophoresis (ECP). We asked EBMT centers if they were willing to provide detailed information on GVHD grading, -therapy, -dosing, -response and complications for each included patient. 31 centers responded positively and we included all patients between 1/2017-7/2019 treated with ECP or ruxolitinib for moderate or severe SR-cGVHD. We identified 84 and 57 patients with ECP and ruxolitinib, respectively. We performed multivariate analyses adjusted on grading and type of SR-cGVHD (steroid dependent vs. refractory vs. intolerant to steroids). At day+180 after initiation of treatment for SR-cGVHD the odds ratio in the ruxolitinib group to achieve overall response vs. the ECP group was 1.35 (95% CI = [0.64; 2.91], p = 0.43). In line, we detected no statistically significant differences in overall survival, progression-free survival, non-relapse mortality and relapse incidence. The clinical significance is limited by the retrospective study design and the current data can't replace prospective studies on ECP in SR-cGVHD. However, the present results contribute to the accumulating evidence on ECP as an effective treatment option in SR-cGVHD.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-03-15T22:56:42.418Z</modification><creation>2025-08-13T03:06:42.464Z</creation></dates><accession>S-EPMC10920188</accession><cross_references><pubmed>38184740</pubmed><doi>10.1038/s41409-023-02174-2</doi></cross_references></HashMap>