<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nakamae H</submitter><funding>Japan Society for the Promotion of Science</funding><pagination>9636897221112098</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9340897</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31</volume><pubmed_abstract>The optimal dose of posttransplant cyclophosphamide (PTCy) for use in patients undergoing HLA-haploidentical hematopoietic cell transplantation with posttransplant cyclophosphamide (PTCy-haplo) has not been sufficiently examined. This study evaluates the safety and efficacy of HLA-haploidentical hematopoietic cell transplantation with a reduced dose of PTCy for patients with a poor prognosis or those with refractory hematological malignancies. We conducted a prospective clinical study of PTCy-haplo with peripheral blood stem cells (PBSCs) using a modified PTCy dosage regimen consisting of 50 mg/kg on day 3 posttransplantation and a reduced dose of 25 mg/kg on day 4. The cumulative incidences of grades II to III and IV acute graft-versus-host disease (GVHD) at day 100 posttransplantation were 30% and 0%, respectively. The cumulative incidence of moderate-to-severe chronic GVHD after transplantation was 7.0%. The cumulative incidence of nonrelapse mortality at 1 year posttransplantation was 6.1%. Overall survival (OS) at 1 year was 66%. In addition, the restricted cubic-spline Cox regression analysis showed nonlinear relationship between the number of infused CD34&lt;sup>+&lt;/sup> cells and CD3&lt;sup>+&lt;/sup> cells, and OS. A graft composition of >4.54 × 10&lt;sup>6&lt;/sup>/kg CD34&lt;sup>+&lt;/sup> cells and >1.85 × 10&lt;sup>8&lt;/sup>/kg but ≤3.70 × 10&lt;sup>8&lt;/sup>/kg CD3&lt;sup>+&lt;/sup> cells was significantly associated with better survival, irrespective of the disease status (hazard ratio, 0.13; 95% confidence interval, 0.04-0.41; &lt;i>P&lt;/i> &lt; 0.001). These results suggest that PTCy-haplo with PBSCs using a de-escalated dose of 50 mg/kg on day 3 and 25 mg/kg on day 4 posttransplantation is a feasible option.</pubmed_abstract><journal>Cell transplantation</journal><pubmed_title>A Prospective Study of an HLA-Haploidentical Peripheral Blood Stem Cell Transplantation Regimen Based on Modification of the Dose of Posttransplant Cyclophosphamide for Poor Prognosis or Refractory Hematological Malignancies.</pubmed_title><pmcid>PMC9340897</pmcid><funding_grant_id>17K09017</funding_grant_id><pubmed_authors>Makuuchi Y</pubmed_authors><pubmed_authors>Nishimoto M</pubmed_authors><pubmed_authors>Nakashima Y</pubmed_authors><pubmed_authors>Kuno M</pubmed_authors><pubmed_authors>Hino M</pubmed_authors><pubmed_authors>Koh H</pubmed_authors><pubmed_authors>Nakamae H</pubmed_authors><pubmed_authors>Okamura H</pubmed_authors><pubmed_authors>Takakuwa T</pubmed_authors><pubmed_authors>Hirose A</pubmed_authors><pubmed_authors>Harada N</pubmed_authors><pubmed_authors>Nakamae M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Prospective Study of an HLA-Haploidentical Peripheral Blood Stem Cell Transplantation Regimen Based on Modification of the Dose of Posttransplant Cyclophosphamide for Poor Prognosis or Refractory Hematological Malignancies.</name><description>The optimal dose of posttransplant cyclophosphamide (PTCy) for use in patients undergoing HLA-haploidentical hematopoietic cell transplantation with posttransplant cyclophosphamide (PTCy-haplo) has not been sufficiently examined. This study evaluates the safety and efficacy of HLA-haploidentical hematopoietic cell transplantation with a reduced dose of PTCy for patients with a poor prognosis or those with refractory hematological malignancies. We conducted a prospective clinical study of PTCy-haplo with peripheral blood stem cells (PBSCs) using a modified PTCy dosage regimen consisting of 50 mg/kg on day 3 posttransplantation and a reduced dose of 25 mg/kg on day 4. The cumulative incidences of grades II to III and IV acute graft-versus-host disease (GVHD) at day 100 posttransplantation were 30% and 0%, respectively. The cumulative incidence of moderate-to-severe chronic GVHD after transplantation was 7.0%. The cumulative incidence of nonrelapse mortality at 1 year posttransplantation was 6.1%. Overall survival (OS) at 1 year was 66%. In addition, the restricted cubic-spline Cox regression analysis showed nonlinear relationship between the number of infused CD34&lt;sup>+&lt;/sup> cells and CD3&lt;sup>+&lt;/sup> cells, and OS. A graft composition of >4.54 × 10&lt;sup>6&lt;/sup>/kg CD34&lt;sup>+&lt;/sup> cells and >1.85 × 10&lt;sup>8&lt;/sup>/kg but ≤3.70 × 10&lt;sup>8&lt;/sup>/kg CD3&lt;sup>+&lt;/sup> cells was significantly associated with better survival, irrespective of the disease status (hazard ratio, 0.13; 95% confidence interval, 0.04-0.41; &lt;i>P&lt;/i> &lt; 0.001). These results suggest that PTCy-haplo with PBSCs using a de-escalated dose of 50 mg/kg on day 3 and 25 mg/kg on day 4 posttransplantation is a feasible option.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan-Dec</publication><modification>2024-10-17T18:59:08.996Z</modification><creation>2024-10-17T18:59:08.996Z</creation></dates><accession>S-EPMC9340897</accession><cross_references><pubmed>35906755</pubmed><doi>10.1177/09636897221112098</doi></cross_references></HashMap>