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Association between the choice of the conditioning regimen and outcomes of allogeneic hematopoietic cell transplantation for myelofibrosis.
Murthy, Guru Subramanian Guru; Kim, Soyoung; Estrada-Merly, Noel; Abid, Muhammad Bilal; Aljurf, Mahmoud; Assal, Amer; Badar, Talha; Badawy, Sherif M; Ballen, Karen; Beitinjaneh, Amer; Cerny, Jan; Chhabra, Saurabh; DeFilipp, Zachariah; Dholaria, Bhagirathbhai; Perez, Miguel Angel Diaz; Farhan, Shatha; Freytes, Cesar O; Gale, Robert Peter; Ganguly, Siddhartha; Gupta, Vikas; Grunwald, Michael R; Hamad, Nada; Hildebrandt, Gerhard C; Inamoto, Yoshihiro; Jain, Tania; Jamy, Omer; Juckett, Mark; Kalaycio, Matt; Krem, Maxwell M; Lazarus, Hillard M; Litzow, Mark; Munker, Reinhold; Murthy, Hemant S; Nathan, Sunita; Nishihori, Taiga; Ortí, Guillermo; Patel, Sagar S; Van der Poel, Marjolein; Rizzieri, David A; Savani, Bipin N; Seo, Sachiko; Solh, Melhem; Verdonck, Leo F; Wirk, Baldeep; Yared, Jean A; Nakamura, Ryotaro; Oran, Betul; Scott, Bart; Saber, Wael.
Afiliação
  • Murthy GSG; Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee. gmurthy@mcw.edu.
  • Kim S; Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI; CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee.
  • Estrada-Merly N; CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee.
  • Abid MB; Divisions of Hematology/Oncology, and Infectious Diseases, Department of Medicine, Medical College of Wisconsin, Milwaukee.
  • Aljurf M; Department of Oncology, King Faisal Specialist Hospital Center and Research, Riyadh.
  • Assal A; Columbia University Irving Medical Center, Department of Medicine, Bone Marrow Transplant and Cell Therapy Program.
  • Badar T; Mayo Clinic, Jacksonville, FL.
  • Badawy SM; Division of Hematology, Oncology and Stem Cell Transplantation, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL; Department of Pediatrics, Northwestern University Feinberg School of Medicine.
  • Ballen K; Division of Hematology/Oncology, University of Virginia Health System, Charlottesville, VA.
  • Beitinjaneh A; Division of Transplantation and Cellular Therapy, University of Miami Hospital and Clinics, Slyvester Comprehensive Cancer Center, Miami, FL.
  • Cerny J; Division of Hematology/Oncology, Department of Medicine, University of Massachusetts Medical Center, Worcester, MA.
  • Chhabra S; CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee.
  • DeFilipp Z; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital.
  • Dholaria B; Vanderbilt University Medical Center, Nashville, TN.
  • Perez MAD; Department of Hematology/Oncology, Hospital Infantil Universitario Niño Jesus, Madrid.
  • Farhan S; Henry Ford Health System Stem Cell Transplant and Cellular Therapy Program, Detroit, MI.
  • Freytes CO; University of Texas Health Science Center at San Antonio, San Antonio, TX.
  • Gale RP; Haematology Research Centre, Department of Immunology and Inflammation, Imperial College London, London.
  • Ganguly S; Division of Hematological Malignancy and Cellular Therapeutics, University of Kansas Health System, Kansas City, KS.
  • Gupta V; MPN Program, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON.
  • Grunwald MR; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, NC.
  • Hamad N; St. Vincent Hospital, Darlinghurst, NSW.
  • Hildebrandt GC; Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Inamoto Y; Division of Hematopoietic Stem Cell Transplantation, National Cancer Center, Tokyo.
  • Jain T; John Hopkins University School of Medicine, Baltimore, MD.
  • Jamy O; University of Alabama at Birmingham, Birmingham, AL.
  • Juckett M; University of Minnesota Blood and Marrow Transplant Program - Adults.
  • Kalaycio M; Cleveland Clinic Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
  • Krem MM; Kansas City VA Medical Center, Kansas City, MO.
  • Lazarus HM; University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH.
  • Litzow M; Division of Hematology and Transplant Center, Mayo Clinic Rochester, Rochester, MN.
  • Munker R; Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Murthy HS; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL.
  • Nathan S; Section of Bone Marrow Transplant and Cell Therapy, Rush University Medical Center.
  • Nishihori T; Department of Blood and Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, FL.
  • Ortí G; Vall d'Hebron University Hospital, Barcelona.
  • Patel SS; Blood and Marrow Transplant Program, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
  • Van der Poel M; Department of Internal Medicine, Division of Hematology, GROW School for Oncology and Developmental Biology, Masstricht University Medical Center, Maastricht.
  • Rizzieri DA; Division of Hematologic Malignancies and Cellular Therapy, Duke University, Durham, NC.
  • Savani BN; Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Seo S; Department of Hematology and Oncology, Dokkyo Medical University, Tochigo.
  • Solh M; The Blood and Marrow Transplant Group of Georgia, Northside Hospital, Atlanta, GA.
  • Verdonck LF; Department of Hematology/Oncology, Isala, Clinic, Zwolle.
  • Wirk B; Bone Marrow Transplant Program, Penn State Cancer Institute, Hershey, Pennsylvania.
  • Yared JA; Transplantation and Cellular Therapy Program, Division of Hematology/Oncology, Department of Medicine, Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD.
  • Nakamura R; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
  • Oran B; Department of Stem Cell Transplantation, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Scott B; Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Saber W; CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee.
Haematologica ; 108(7): 1900-1908, 2023 Jul 01.
Article em En | MEDLINE | ID: mdl-36779595
ABSTRACT
Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only curative treatment for myelofibrosis. However, the optimal conditioning regimen either with reduced-intensity conditioning (RIC) or myeloablative conditioning (MAC) is not well known. Using the Center for International Blood and Marrow Transplant Research database, we identified adults aged ≥18 years with myelofibrosis undergoing allo-HCT between 2008-2019 and analyzed the outcomes separately in the RIC and MAC cohorts based on the conditioning regimens used. Among 872 eligible patients, 493 underwent allo-HCT using RIC (fludarabine/ busulfan n=166, fludarabine/melphalan n=327) and 379 using MAC (fludarabine/busulfan n=247, busulfan/cyclophosphamide n=132). In multivariable analysis with RIC, fludarabine/melphalan was associated with inferior overall survival (hazard ratio [HR]=1.80; 95% confidenec interval [CI] 1.15-2.81; P=0.009), higher early non-relapse mortality (HR=1.81; 95% CI 1.12-2.91; P=0.01) and higher acute graft-versus-host disease (GvHD) (grade 2-4 HR=1.45; 95% CI 1.03-2.03; P=0.03; grade 3-4 HR=2.21; 95%CI 1.28-3.83; P=0.004) compared to fludarabine/busulfan. In the MAC setting, busulfan/cyclophosphamide was associated with a higher acute GvHD (grade 2-4 HR=2.33; 95% CI 1.67-3.25; P<0.001; grade 3-4 HR=2.31; 95% CI 1.52-3.52; P<0.001) and inferior GvHD-free relapse-free survival (GRFS) (HR=1.94; 95% CI 1.49-2.53; P<0.001) as compared to fludarabine/busulfan. Hence, our study suggests that fludarabine/busulfan is associated with better outcomes in RIC (better overall survival, lower early non-relapse mortality, lower acute GvHD) and MAC (lower acute GvHD and better GRFS) in myelofibrosis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Mielofibrose Primária / Doença Enxerto-Hospedeiro Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Humans Idioma: En Revista: Haematologica Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Mielofibrose Primária / Doença Enxerto-Hospedeiro Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Humans Idioma: En Revista: Haematologica Ano de publicação: 2023 Tipo de documento: Article