<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Askar M</submitter><funding>Allogen Laboratories</funding><funding>Takeda Oncology; Telomere Diagnostics, Inc.</funding><funding>NHLBI NIH HHS</funding><funding>Janssen Scientific Affairs, LLC</funding><funding>Alexion</funding><funding>Gamida Cell Ltd.</funding><funding>American Cancer Society</funding><funding>Spectrum Pharmaceuticals, Inc.</funding><funding>Novartis Pharmaceuticals Corporation</funding><funding>Otsuka America Pharmaceutical, Inc.</funding><funding>MesoScale Diagnostics, Inc.</funding><funding>The Medical College of Wisconsin</funding><funding>Match Foundation</funding><funding>AstraZeneca</funding><funding>US National Marrow Donor Program (NMDP) Immunobiology Research Grant Program</funding><funding>Intramural NIH HHS</funding><funding>Optum Healthcare Solutions, Inc.</funding><funding>Cellular Dynamics International, Inc.</funding><funding>Medical College of Wisconsin</funding><funding>Onyx Pharmaceuticals</funding><funding>Jazz Pharmaceuticals, Inc.</funding><funding>Otsuka Pharmaceutical Co, Ltd. – Japan</funding><funding>Genentech, Inc.</funding><funding>Amgen, Inc.</funding><funding>University of Minnesota</funding><funding>The Leukemia &amp;amp; Lym phoma Society</funding><funding>Miltenyi Biotec, Inc.</funding><funding>Medac, GmbH</funding><funding>Mesoblast</funding><funding>Sunesis Pharmaceuticals, Inc.</funding><funding>Health Research, Inc. Roswell Park Cancer Institute</funding><funding>Jeff Gordon Children&amp;apos;s Foundation</funding><funding>Incyte Corporation</funding><funding>Bluebird Bio, Inc.</funding><funding>HistoGenetics, Inc.</funding><funding>Chimerix, Inc.</funding><funding>National Marrow Donor Program</funding><funding>Wellpoint, Inc.</funding><funding>National Cancer Institute</funding><funding>Bristol Myers Squibb Oncology</funding><funding>Seattle Genetics</funding><funding>Celgene Corporation</funding><funding>Pfizer, Inc</funding><funding>Neovii Biotech NA, Inc.</funding><funding>Gilead Sciences, Inc.</funding><funding>St. Baldrick&amp;apos;s Foundation</funding><funding>Swedish Orphan Biovitrum, Inc.</funding><funding>Sanofi US</funding><funding>Health Resources and Services Administration</funding><funding>Cleveland Clinic Foundation</funding><funding>Office of Naval Research</funding><funding>MedImmune</funding><funding>National Institute of Allergy and Infectious Diseases</funding><funding>National Heart, Lung and Blood Institute</funding><funding>Perkin Elmer, Inc.</funding><funding>Astellas Pharma US</funding><funding>Fred Hutchinson Cancer Research Center</funding><funding>PCORI</funding><funding>NCI NIH HHS</funding><funding>Genzyme Corporation</funding><funding>Merck &amp;amp; Co, Inc.</funding><pagination>436-444</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5370205</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(3)</volume><pubmed_abstract>Single-center studies have previously reported associations of MHC Class I Chain-Related Gene A (MICA) polymorphisms and donor-recipient MICA mismatching with graft-versus-host disease (GVHD) after unrelated donor hematopoietic cell transplantation (HCT). In this study, we investigated the association of MICA polymorphism (MICA-129, MM versus MV versus VV) and MICA mismatches after HCT with 10/10 HLA-matched (n = 552) or 9/10 (n = 161) unrelated donors. Included were adult patients with a first unrelated bone marrow or peripheral blood HCT for acute lymphoblastic leukemia, acute myeloid leukemia, or myelodysplastic syndrome that were reported to the Center for International Blood and Marrow Transplant Research between 1999 and 2011. Our results showed that neither MICA mismatch nor MICA-129 polymorphism were associated with any transplantation outcome (P &lt; .01), with the exception of a higher relapse in recipients of MICA-mismatched HLA 10/10 donors (hazard ratio [HR], 1.7; P = .003). There was a suggestion of association between MICA mismatches and a higher risk of acute GVHD grades II to IV (HR, 1.4; P = .013) There were no significant interactions between MICA mismatches and HLA matching (9/10 versus 10/10). In conclusion, the findings in this cohort did not confirm prior studies reporting that MICA polymorphism and MICA mismatches were associated with HCT outcomes.</pubmed_abstract><journal>Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation</journal><pubmed_title>MHC Class I Chain-Related Gene A (MICA) Donor-Recipient Mismatches and MICA-129 Polymorphism in Unrelated Donor Hematopoietic Cell Transplantations Has No Impact on Outcomes in Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, or Myelodysplastic Syndrome: A Center for International Blood and Marrow Transplant Research Study.</pubmed_title><pmcid>PMC5370205</pmcid><funding_grant_id>5U24-CA076518</funding_grant_id><funding_grant_id>N00014-15-1-0848</funding_grant_id><funding_grant_id>N00014-16-1-2020</funding_grant_id><funding_grant_id>IRG-91-022-18</funding_grant_id><funding_grant_id>ZIA LM000022-18</funding_grant_id><funding_grant_id>P01 CA023766</funding_grant_id><funding_grant_id>U10 HL069294</funding_grant_id><funding_grant_id>HHSH250201200016C</funding_grant_id><funding_grant_id>U24 CA076518</funding_grant_id><funding_grant_id>5U10HL069294</funding_grant_id><pubmed_authors>Fernandez-Vina M</pubmed_authors><pubmed_authors>Lee SJ</pubmed_authors><pubmed_authors>Sobecks R</pubmed_authors><pubmed_authors>Thomas D</pubmed_authors><pubmed_authors>Fleischhauer K</pubmed_authors><pubmed_authors>Madbouly A</pubmed_authors><pubmed_authors>Askar M</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Haagenson M</pubmed_authors><pubmed_authors>Hsu K</pubmed_authors><pubmed_authors>Majhail N</pubmed_authors><pubmed_authors>Spellman SR</pubmed_authors><pubmed_authors>Zhang A</pubmed_authors><pubmed_authors>Verneris M</pubmed_authors></additional><is_claimable>false</is_claimable><name>MHC Class I Chain-Related Gene A (MICA) Donor-Recipient Mismatches and MICA-129 Polymorphism in Unrelated Donor Hematopoietic Cell Transplantations Has No Impact on Outcomes in Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, or Myelodysplastic Syndrome: A Center for International Blood and Marrow Transplant Research Study.</name><description>Single-center studies have previously reported associations of MHC Class I Chain-Related Gene A (MICA) polymorphisms and donor-recipient MICA mismatching with graft-versus-host disease (GVHD) after unrelated donor hematopoietic cell transplantation (HCT). In this study, we investigated the association of MICA polymorphism (MICA-129, MM versus MV versus VV) and MICA mismatches after HCT with 10/10 HLA-matched (n = 552) or 9/10 (n = 161) unrelated donors. Included were adult patients with a first unrelated bone marrow or peripheral blood HCT for acute lymphoblastic leukemia, acute myeloid leukemia, or myelodysplastic syndrome that were reported to the Center for International Blood and Marrow Transplant Research between 1999 and 2011. Our results showed that neither MICA mismatch nor MICA-129 polymorphism were associated with any transplantation outcome (P &lt; .01), with the exception of a higher relapse in recipients of MICA-mismatched HLA 10/10 donors (hazard ratio [HR], 1.7; P = .003). There was a suggestion of association between MICA mismatches and a higher risk of acute GVHD grades II to IV (HR, 1.4; P = .013) There were no significant interactions between MICA mismatches and HLA matching (9/10 versus 10/10). In conclusion, the findings in this cohort did not confirm prior studies reporting that MICA polymorphism and MICA mismatches were associated with HCT outcomes.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2024-11-12T11:04:11.362Z</modification><creation>2019-03-26T23:04:33Z</creation></dates><accession>S-EPMC5370205</accession><cross_references><pubmed>27987385</pubmed><doi>10.1016/j.bbmt.2016.11.021</doi></cross_references></HashMap>