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Myeloablative vs reduced intensity T-cell-replete haploidentical transplantation for hematologic malignancy.
Solomon, Scott R; St Martin, Andrew; Shah, Nirav N; Fatobene, Giancarlo; Al Malki, Monzr M; Ballen, Karen K; Bashey, Asad; Bejanyan, Nelli; Bolaños Meade, Javier; Brunstein, Claudio G; DeFilipp, Zachariah; Champlin, Richard E; Fuchs, Ephraim J; Hamadani, Mehdi; Hematti, Peiman; Kanakry, Christopher G; McGuirk, Joseph P; McNiece, Ian K; Ciurea, Stefan O; Pasquini, Marcelo C; Rocha, Vanderson; Romee, Rizwan; Patel, Sagar S; Vasu, Sumithira; Waller, Edmund K; Wingard, John R; Zhang, Mei-Jie; Eapen, Mary.
Affiliation
  • Solomon SR; The Blood and Marrow Transplant Program, Northside Hospital, Atlanta, GA.
  • St Martin A; Center for International Blood and Marrow Transplant Research, and.
  • Shah NN; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
  • Fatobene G; Hospital das Clinicas da Universidade de São Paulo, São Paulo, Brazil.
  • Al Malki MM; Department of Hematology & Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
  • Ballen KK; Division of Hematology/Oncology, University of Virginia Health System, Charlottesville, VA.
  • Bashey A; The Blood and Marrow Transplant Program, Northside Hospital, Atlanta, GA.
  • Bejanyan N; H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
  • Bolaños Meade J; The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.
  • Brunstein CG; University of Minnesota Medical Center, Minneapolis, MN.
  • DeFilipp Z; Winship Cancer Institute, Massachusetts General Hospital, Boston, MA.
  • Champlin RE; University of Texas MD Anderson Cancer Center, Houston, TX.
  • Fuchs EJ; The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.
  • Hamadani M; Center for International Blood and Marrow Transplant Research, and.
  • Hematti P; Division of Hematology/Oncology/Bone Marrow Transplantation, Department of Medicine, University of Wisconsin Hospital and Clinics, University of Wisconsin, Madison, WI.
  • Kanakry CG; National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • McGuirk JP; Division of Hematologic Malignancies and Cellular Therapy, University of Kansas Medical Center, Kansas City, KS.
  • McNiece IK; CellMED Consulting, Miami, FL.
  • Ciurea SO; University of Texas MD Anderson Cancer Center, Houston, TX.
  • Pasquini MC; Center for International Blood and Marrow Transplant Research, and.
  • Rocha V; Hospital das Clinicas da Universidade de São Paulo, São Paulo, Brazil.
  • Romee R; Department of Haematology, University of Oxford, Oxford, United Kingdom.
  • Patel SS; Division of Hematologic Malignancies and Transplantation, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
  • Vasu S; Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
  • Waller EK; Division of Hematology, The Ohio State University Comprehensive Cancer Center, Columbus, OH.
  • Wingard JR; Department of Hematology and Medical Oncology, Winship Cancer Institute, Atlanta, GA; and.
  • Zhang MJ; Division of Heamtology & Oncology, Department of Medicine, University of Florida, Gainesville, FL.
  • Eapen M; Center for International Blood and Marrow Transplant Research, and.
Blood Adv ; 3(19): 2836-2844, 2019 10 08.
Article in En | MEDLINE | ID: mdl-31582392
ABSTRACT
In the absence of prospective studies that examine the effect of conditioning regimen intensity after T-cell-replete haploidentical transplant for acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), and myelodysplastic syndrome (MDS), a retrospective cohort analysis was performed. Of the 1325 eligible patients (AML, n = 818; ALL, n = 286; and MDS, n = 221), 526 patients received a myeloablative regimen and 799 received a reduced-intensity regimen. Graft-versus-host disease prophylaxis was uniform with posttransplant cyclophosphamide, a calcineurin inhibitor, and mycophenolate mofetil. The primary end point was disease-free survival. Cox regression models were built to study the effect of conditioning regimen intensity on transplant outcomes. For patients aged 18 to 54 years, disease-free survival was lower (hazard ratio [HR], 1.34; 42% vs 51%; P = .007) and relapse was higher (HR, 1.51; 44% vs 33%; P = .001) with a reduced-intensity regimen compared with a myeloablative regimen. Nonrelapse mortality did not differ according to regimen intensity. For patients aged 55 to 70 years, disease-free survival (HR, 0.97; 37% vs 43%; P = .83) and relapse (HR, 1.32; 42% vs 31%; P = .11) did not differ according to regimen intensity. Nonrelapse mortality was lower with reduced-intensity regimens (HR, 0.64; 20% vs 31%; P = .02). Myeloablative regimens are preferred for AML, ALL, and MDS; reduced-intensity regimens should be reserved for those unable to tolerate myeloablation.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Hematologic Neoplasms / Transplantation Conditioning / Myeloablative Agonists / Transplantation, Haploidentical Type of study: Observational_studies Limits: Adolescent / Adult / Female / Humans / Middle aged Language: En Journal: Blood Adv Year: 2019 Type: Article Affiliation country: Gabon

Full text: 1 Database: MEDLINE Main subject: Hematologic Neoplasms / Transplantation Conditioning / Myeloablative Agonists / Transplantation, Haploidentical Type of study: Observational_studies Limits: Adolescent / Adult / Female / Humans / Middle aged Language: En Journal: Blood Adv Year: 2019 Type: Article Affiliation country: Gabon