Your browser doesn't support javascript.
loading
Characteristics of Graft-Versus-Host Disease (GvHD) After Post-Transplantation Cyclophosphamide Versus Conventional GvHD Prophylaxis.
Saliba, Rima M; Alousi, Amin M; Pidala, Joseph; Arora, Mukta; Spellman, Stephen R; Hemmer, Michael T; Wang, Tao; Abboud, Camille; Ahmed, Sairah; Antin, Joseph H; Beitinjaneh, Amer; Buchbinder, David; Byrne, Michael; Cahn, Jean-Yves; Choe, Hannah; Hanna, Rabi; Hematti, Peiman; Kamble, Rammurti T; Kitko, Carrie L; Laughlin, Mary; Lekakis, Lazaros; MacMillan, Margaret L; Martino, Rodrigo; Mehta, Parinda A; Nishihori, Taiga; Patel, Sagar S; Perales, Miguel-Angel; Rangarajan, Hemalatha G; Ringdén, Olov; Rosenthal, Joseph; Savani, Bipin N; Schultz, Kirk R; Seo, Sachiko; Teshima, Takanori; van der Poel, Marjolein; Verdonck, Leo F; Weisdorf, Daniel; Wirk, Baldeep; Yared, Jean A; Schriber, Jeffrey; Champlin, Richard E; Ciurea, Stefan O.
Affiliation
  • Saliba RM; Department of Stem Cell Transplantation and Cellular Therapy, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas. Electronic address: rsaliba@mdanderson.org.
  • Alousi AM; Department of Stem Cell Transplantation and Cellular Therapy, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Pidala J; H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Arora M; CIBMTR® (Center for International Blood and Marrow Transplant Research), National Marrow Donor Program/Be the Match, Minneapolis, Minnesota; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota Medical Center, Minneapolis, Minnesota.
  • Spellman SR; CIBMTR® (Center for International Blood and Marrow Transplant Research), National Marrow Donor Program/Be the Match, Minneapolis, Minnesota.
  • Hemmer MT; CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Wang T; CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Divsion of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Abboud C; Washington University in St. Louis School of Medicine, Division of Oncology, Section of BMT and Leukemia, St. Louis, Missouri.
  • Ahmed S; Department of Lymphoma-Myeloma, The University of Texas, MD Anderson Cancer Center, Houston, Texas.
  • Antin JH; Division of Hematologic Malignancies, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Beitinjaneh A; Division of Transplantation and Cellular Therapy, University of Miami Hospital and Clinics, Sylvester Comprehensive Cancer Center, Miami, Florida.
  • Buchbinder D; Division of Pediatric Hematology, Children's Hospital of Orange County, Orange, California.
  • Byrne M; Vanderbilt University Medical Center, Nashville, Tennessee.
  • Cahn JY; Department of Hematology, CHU Grenoble Alpes, Université Grenoble Alpes, Grenoble, France.
  • Choe H; The Ohio State University Wexner Medical Center, James Comprehensive Cancer Center, Columbus, Ohio.
  • Hanna R; Cleveland Clinic, Cleveland, Ohio.
  • Hematti P; Division of Hematology/Oncology/Bone Marrow Transplantation, Department of Medicine, University of Wisconsin, Madison, Wisconsin.
  • Kamble RT; Division of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
  • Kitko CL; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Laughlin M; Medical Director, Cleveland Cord Blood Center, Cleveland, Ohio.
  • Lekakis L; Division of Transplantation and Cellular Therapy, University of Miami Hospital and Clinics, Sylvester Comprehensive Cancer Center, Miami, Florida.
  • MacMillan ML; Blood and Marrow Transplant Program, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota.
  • Martino R; Division of Clinical Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Mehta PA; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Nishihori T; Department of Blood & Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, Florida.
  • Patel SS; Blood and Marrow Transplant Program, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah.
  • Perales MA; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Rangarajan HG; Department of Pediatric Hematology, Oncology, Blood and Marrow Transplantation, Nationwide Children's Hospital, Columbus, Ohio.
  • Ringdén O; Translational Cell Therapy Group, CLINTEC (Clinical Science, Intervention and Technology), Karolinska Institutet, Stockholm, Sweden.
  • Rosenthal J; City of Hope, Duarte, California.
  • Savani BN; Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Schultz KR; Department of Pediatric Hematology, Oncology and Bone Marrow Transplant, British Columbia's Children's Hospital, The University of British Columbia, Vancouver, British Columbia, Canada.
  • Seo S; Department of Hematology and Oncology, Dokkyo Medical University, Tochigi, Japan.
  • Teshima T; Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo, Japan.
  • van der Poel M; Department of Internal Medicine, Division of Hematology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Verdonck LF; Department of Hematology/Oncology, Isala Clinic, Zwolle, The Netherlands.
  • Weisdorf D; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minnesota.
  • Wirk B; Bone Marrow Transplant Program, Penn State Cancer Institute, Hershey, Pennsylvania.
  • Yared JA; Transplantation & Cellular Therapy Program, Division of Hematology/Oncology, Department of Medicine, Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, Maryland.
  • Schriber J; Cancer Treatment Centers of America Comprehensive Care and Research Center, Phoenix, Arizona.
  • Champlin RE; Department of Stem Cell Transplantation and Cellular Therapy, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Ciurea SO; Hematopoietic Stem Cell Transplantation and Cellular Therapy Program, University of California, Irvine, Orange, California.
Transplant Cell Ther ; 28(10): 681-693, 2022 10.
Article in En | MEDLINE | ID: mdl-35853610
ABSTRACT
Post-transplantation cyclophosphamide (PTCy) has been shown to effectively control graft-versus-host disease (GvHD) in haploidentical (Haplo) transplantations. In this retrospective registry study, we compared GvHD organ distribution, severity, and outcomes in patients with GvHD occurring after Haplo transplantation with PTCy GvHD prophylaxis (Haplo/PTCy) versus HLA-matched unrelated donor transplantation with conventional prophylaxis (MUD/conventional). We evaluated 2 cohorts patients with grade 2 to 4 acute GvHD (aGvHD) including 264 and 1163 recipients of Haplo and MUD transplants; and patients with any chronic GvHD (cGvHD) including 206 and 1018 recipients of Haplo and MUD transplants, respectively. In comparison with MUD/conventional transplantation ± antithymocyte globulin (ATG), grade 3-4 aGvHD (28% versus 39%, P = .001), stage 3-4 lower gastrointestinal (GI) tract aGvHD (14% versus 21%, P = .01), and chronic GI GvHD (21% versus 31%, P = .006) were less common after Haplo/PTCy transplantation. In patients with grade 2-4 aGvHD, cGvHD rate after Haplo/PTCY was also lower (hazard ratio [HR] = .4, P < .001) in comparison with MUD/conventional transplantation without ATG in the nonmyeloablative conditioning setting. Irrespective of the use of ATG, non-relapse mortality rate was lower (HR = .6, P = .01) after Haplo/PTCy transplantation, except for transplants that were from a female donor into a male recipient. In patients with cGvHD, irrespective of ATG use, Haplo/PTCy transplantation had lower non-relapse mortality rates (HR = .6, P = .04). Mortality rate was higher (HR = 1.6, P = .03) during, but not after (HR = .9, P = .6) the first 6 months after cGvHD diagnosis. Our results suggest that PTCy-based GvHD prophylaxis mitigates the development of GI GvHD and may translate into lower GvHD-related non-relapse mortality rate.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Graft vs Host Disease Type of study: Observational_studies Limits: Female / Humans / Male Language: En Journal: Transplant Cell Ther Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Graft vs Host Disease Type of study: Observational_studies Limits: Female / Humans / Male Language: En Journal: Transplant Cell Ther Year: 2022 Document type: Article