<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cusatis R</submitter><funding>Takeda Pharmaceuticals U.S.A.</funding><funding>GlaxoSmithKline</funding><funding>Amgen</funding><funding>Bristol Myers Squibb Co.</funding><funding>CareDx</funding><funding>Actinium Pharmaceuticals</funding><funding>NHLBI NIH HHS</funding><funding>Pharmacyclics</funding><funding>MorphoSys</funding><funding>Adaptive Biotechnologies</funding><funding>Merck</funding><funding>Kiadis Pharma</funding><funding>Karyopharm Therapeutics</funding><funding>Novartis Pharmaceuticals Corporation</funding><funding>Sanofi Genzyme</funding><funding>National Cancer Institute</funding><funding>CytoSen Therapeutics</funding><funding>Kyowa Kirin</funding><funding>Seagen</funding><funding>Incyte</funding><funding>Medac</funding><funding>Accenture</funding><funding>Pfizer</funding><funding>Medical College of Wisconsin</funding><funding>Health Resources and Services Administration</funding><funding>AbbVie</funding><funding>Office of Naval Research</funding><funding>National Institute of Allergy and Infectious Diseases</funding><funding>Janssen Biotech</funding><funding>Miltenyi Biotec</funding><funding>Genentech</funding><funding>bluebird bio</funding><funding>Astellas Pharma US</funding><funding>Omeros Corporation</funding><funding>Be The Match Foundation</funding><funding>NCI NIH HHS</funding><funding>Daiichi Sankyo Co., Ltd.</funding><funding>Jazz Pharmaceuticals</funding><funding>Gilead</funding><funding>StemCyte</funding><pagination>229-250</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9839494</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>98(2)</volume><pubmed_abstract>For myelodysplastic syndrome (MDS), allogeneic hematopoietic cell transplantation (alloHCT) is the only available curative therapy. The Blood and Marrow Transplant Clinical Trials Network study 1102 (BMT CTN 1102, NCT02016781) was a multicenter, biologic assignment trial based on matched donor availability in adults aged 50-75 with higher risk de novo MDS who were candidates for reduced-intensity conditioning (RIC) alloHCT. The primary analysis showed that those who received alloHCT had a survival benefit, but whether this is at the cost of worse quality of life (QOL) has not been described in detail. English- and Spanish-speaking trial participants completed the Functional Assessment of Cancer Therapy-General (FACT-G), the SF-36, and the EQ-5D, at enrollment, every 6 months until 24 month</pubmed_abstract><journal>American journal of hematology</journal><pubmed_title>Health-related quality of life in reduced-intensity hematopoietic cell transplantation based on donor availability in patients aged 50-75 with advanced myelodysplastic syndrome: BMT CTN 1102.</pubmed_title><pmcid>PMC9839494</pmcid><funding_grant_id>U24 HL138660</funding_grant_id><funding_grant_id>U10 HL069294</funding_grant_id><funding_grant_id>UG1 HL069246</funding_grant_id><funding_grant_id>U24HL138660</funding_grant_id><funding_grant_id>U24 CA076518</funding_grant_id><funding_grant_id>U24CA076518</funding_grant_id><funding_grant_id>U10HL069294</funding_grant_id><pubmed_authors>Gregory A</pubmed_authors><pubmed_authors>Lee SJ</pubmed_authors><pubmed_authors>Logan BR</pubmed_authors><pubmed_authors>Saber W</pubmed_authors><pubmed_authors>Cusatis R</pubmed_authors><pubmed_authors>Flynn KE</pubmed_authors><pubmed_authors>D'Souza A</pubmed_authors><pubmed_authors>Hamilton BK</pubmed_authors><pubmed_authors>Cutler CS</pubmed_authors><pubmed_authors>Shaw BE</pubmed_authors><pubmed_authors>Martens MJ</pubmed_authors><pubmed_authors>Horowitz MM</pubmed_authors><pubmed_authors>Nakamura R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Health-related quality of life in reduced-intensity hematopoietic cell transplantation based on donor availability in patients aged 50-75 with advanced myelodysplastic syndrome: BMT CTN 1102.</name><description>For myelodysplastic syndrome (MDS), allogeneic hematopoietic cell transplantation (alloHCT) is the only available curative therapy. The Blood and Marrow Transplant Clinical Trials Network study 1102 (BMT CTN 1102, NCT02016781) was a multicenter, biologic assignment trial based on matched donor availability in adults aged 50-75 with higher risk de novo MDS who were candidates for reduced-intensity conditioning (RIC) alloHCT. The primary analysis showed that those who received alloHCT had a survival benefit, but whether this is at the cost of worse quality of life (QOL) has not been described in detail. English- and Spanish-speaking trial participants completed the Functional Assessment of Cancer Therapy-General (FACT-G), the SF-36, and the EQ-5D, at enrollment, every 6 months until 24 month</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-26T11:47:24.239Z</modification><creation>2025-02-19T04:59:40.471Z</creation></dates><accession>S-EPMC9839494</accession><cross_references><pubmed>36251401</pubmed><doi>10.1002/ajh.26768</doi></cross_references></HashMap>