<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>103(2)</volume><submitter>Schmid C</submitter><pubmed_abstract>No standard exists for the treatment of myelodysplastic syndrome relapsing after allogeneic stem cell transplantation. We performed a retrospective registry analysis of outcomes and risk factors in 698 patients, treated with different strategies. The median overall survival from relapse was 4.7 months (95% confidence interval: 4.1-5.3) and the 2-year survival rate was 17.7% (95% confidence interval: 14.8-21.2%). Shorter remission after transplantation (P&lt;0.001), advanced disease (P=0.001), older age (P=0.007), unrelated donor (P=0.008) and acute graft-versus-host disease before relapse (P&lt;0.001) adversely influenced survival. At 6 months from relapse, patients had received no cellular treatment, (i.e. palliative chemotherapy or best supportive care, n=375), donor lymphocyte infusion (n=213</pubmed_abstract><journal>Haematologica</journal><pagination>237-245</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5792268</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Outcome after relapse of myelodysplastic syndrome and secondary acute myeloid leukemia following allogeneic stem cell transplantation: a retrospective registry analysis on 698 patients by the Chronic Malignancies Working Party of the European Society of Blood and Marrow Transplantation.</pubmed_title><pmcid>PMC5792268</pmcid><pubmed_authors>Schmid C</pubmed_authors><pubmed_authors>Mufti G</pubmed_authors><pubmed_authors>Cornelissen JJ</pubmed_authors><pubmed_authors>Robin M</pubmed_authors><pubmed_authors>Beelen D</pubmed_authors><pubmed_authors>Arnold R</pubmed_authors><pubmed_authors>Finke J</pubmed_authors><pubmed_authors>Veelken H</pubmed_authors><pubmed_authors>Niederwieser D</pubmed_authors><pubmed_authors>Milpied N</pubmed_authors><pubmed_authors>de Witte T</pubmed_authors><pubmed_authors>Ehninger G</pubmed_authors><pubmed_authors>Gramatzki M</pubmed_authors><pubmed_authors>Maertens J</pubmed_authors><pubmed_authors>Yakoub-Agha I</pubmed_authors><pubmed_authors>Rovira M</pubmed_authors><pubmed_authors>van Biezen A</pubmed_authors><pubmed_authors>Volin L</pubmed_authors><pubmed_authors>Ganser A</pubmed_authors><pubmed_authors>Kanz L</pubmed_authors><pubmed_authors>Passweg J</pubmed_authors><pubmed_authors>Alessandrino P</pubmed_authors><pubmed_authors>de Wreede LC</pubmed_authors><pubmed_authors>Kroger N</pubmed_authors><pubmed_authors>Blaise D</pubmed_authors><pubmed_authors>Schleuning M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcome after relapse of myelodysplastic syndrome and secondary acute myeloid leukemia following allogeneic stem cell transplantation: a retrospective registry analysis on 698 patients by the Chronic Malignancies Working Party of the European Society of Blood and Marrow Transplantation.</name><description>No standard exists for the treatment of myelodysplastic syndrome relapsing after allogeneic stem cell transplantation. We performed a retrospective registry analysis of outcomes and risk factors in 698 patients, treated with different strategies. The median overall survival from relapse was 4.7 months (95% confidence interval: 4.1-5.3) and the 2-year survival rate was 17.7% (95% confidence interval: 14.8-21.2%). Shorter remission after transplantation (P&lt;0.001), advanced disease (P=0.001), older age (P=0.007), unrelated donor (P=0.008) and acute graft-versus-host disease before relapse (P&lt;0.001) adversely influenced survival. At 6 months from relapse, patients had received no cellular treatment, (i.e. palliative chemotherapy or best supportive care, n=375), donor lymphocyte infusion (n=213</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Feb</publication><modification>2025-04-19T02:04:03.063Z</modification><creation>2019-07-24T07:12:39Z</creation></dates><accession>S-EPMC5792268</accession><cross_references><pubmed>29101205</pubmed><doi>10.3324/haematol.2017.168716</doi></cross_references></HashMap>