<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Muniz P</submitter><pubmed_abstract>Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative treatment for patients with hematologic malignances. Haploidentical HSCT (Haplo-HSCT) is an alternative option for patients who do not have an HLA-matched donor. The use of post-transplantation high dose cyclophosphamide (PT-Cy) is commonly employed for graft-versus-host disease (GVHD) prophylaxis in haplo-HSCT. Cyclophosphamide (Cy) is an alkylating agent with antineoplastic and immunosuppressive activity, whose bioactivation requires the activity of polymorphic enzymes in the liver to produce phosphoramide mustard, which is a DNA alkylating agent. To identify polymorphisms in the genes of Cy metabolism and correlate them with post-HSCT complications [GVHD, sinusoidal obstruction syndrome (SOS), hemorrhagic cysti</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1002959</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9537744</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association between gene polymorphisms in the cyclophosphamide metabolism pathway with complications after haploidentical hematopoietic stem cell transplantation.</pubmed_title><pmcid>PMC9537744</pmcid><pubmed_authors>Muniz P</pubmed_authors><pubmed_authors>Dorado N</pubmed_authors><pubmed_authors>Kwon M</pubmed_authors><pubmed_authors>Bailen R</pubmed_authors><pubmed_authors>Martinez-Laperche C</pubmed_authors><pubmed_authors>Diez-Martin JL</pubmed_authors><pubmed_authors>Anguita J</pubmed_authors><pubmed_authors>Andres-Zayas C</pubmed_authors><pubmed_authors>Gallardo D</pubmed_authors><pubmed_authors>Gomez Centurion I</pubmed_authors><pubmed_authors>Carbonell D</pubmed_authors><pubmed_authors>Buno I</pubmed_authors><pubmed_authors>Chicano M</pubmed_authors><pubmed_authors>Suarez-Gonzalez J</pubmed_authors><pubmed_authors>Oarbeascoa G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association between gene polymorphisms in the cyclophosphamide metabolism pathway with complications after haploidentical hematopoietic stem cell transplantation.</name><description>Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative treatment for patients with hematologic malignances. Haploidentical HSCT (Haplo-HSCT) is an alternative option for patients who do not have an HLA-matched donor. The use of post-transplantation high dose cyclophosphamide (PT-Cy) is commonly employed for graft-versus-host disease (GVHD) prophylaxis in haplo-HSCT. Cyclophosphamide (Cy) is an alkylating agent with antineoplastic and immunosuppressive activity, whose bioactivation requires the activity of polymorphic enzymes in the liver to produce phosphoramide mustard, which is a DNA alkylating agent. To identify polymorphisms in the genes of Cy metabolism and correlate them with post-HSCT complications [GVHD, sinusoidal obstruction syndrome (SOS), hemorrhagic cysti</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-31T16:06:04.69Z</modification><creation>2025-02-19T01:28:13.577Z</creation></dates><accession>S-EPMC9537744</accession><cross_references><pubmed>36211438</pubmed><doi>10.3389/fimmu.2022.1002959</doi></cross_references></HashMap>