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Prospective analysis to determine barriers to allogeneic hematopoietic cell transplantation in patients with acute leukemia.
Nath, Karthik; Lee, Jasme; Elko, Theresa A; Levy, Lauren; Preston, Elaina; Devlin, Sean M; Ponce, Doris M; Lin, Richard J; Shaffer, Brian C; Cho, Christina; Politikos, Ioannis; Jakubowski, Ann A; Park, Jae H; Rampal, Raajit; Perales, Miguel-Angel; Tallman, Martin S; Barker, Juliet N; Berman, Ellin; Tamari, Roni; Stein, Eytan; Giralt, Sergio A; Gyurkocza, Boglarka.
Affiliation
  • Nath K; Cellular Therapy Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Lee J; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Elko TA; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Levy L; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Preston E; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Devlin SM; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Ponce DM; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Lin RJ; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Shaffer BC; Cellular Therapy Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Cho C; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Politikos I; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Jakubowski AA; Cellular Therapy Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Park JH; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Rampal R; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Perales MA; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Tallman MS; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Barker JN; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Berman E; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Tamari R; Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Stein E; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Giralt SA; Cellular Therapy Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Gyurkocza B; Department of Medicine, Weill Cornell Medical College, New York, New York, USA.
Am J Hematol ; 98(12): 1869-1876, 2023 12.
Article in En | MEDLINE | ID: mdl-37688521
ABSTRACT
Allogeneic hematopoietic cell transplantation (allo-HCT) is a potentially curative treatment for patients with acute leukemia. Despite this, studies have shown that only a minority of patients ultimately proceed to allo-HCT. The primary objective of this prospective, observational study was to identify the rate of allo-HCT in patients for whom it was recommended, and reasons why patients deemed appropriate and eligible for HCT did not subsequently undergo transplant. Between April 2016 and April 2021, adult patients with newly diagnosed or relapsed/refractory acute leukemia were enrolled at the time of induction/reinduction therapy. Initial transplantation workup and allo-HCT recommendations were made during the early phase of induction/reinduction. Of the 307 enrolled patients, allo-HCT was recommended to 85% (n = 259), of whom 66% (n = 170) underwent transplant. Donor sources comprised 54% human leukocyte antigen (HLA)-matched unrelated donors, 20% HLA-matched sibling donors and HLA-mismatched graft sources with 15% umbilical cord blood units, 8% HLA-mismatched unrelated donors, and 4% HLA-haploidentical donors. The most common reason for transplant disqualification in the 89 patients in whom it was initially recommended was persistent/relapsed disease (70%), followed by early patient death (10%). In this prospective study, we report a high allo-HCT rate, which may be due to early transplant referral and workup. The main allo-HCT barrier was disease control, followed by early patient death. With the increasing availability of HLA-mismatched graft sources, the lack of donor availability was not a transplant barrier. Further development of novel transplant strategies for patients not achieving remission and improvements in induction regimens could result in increased allo-HCT utilization.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Hematopoietic Stem Cell Transplantation / Graft vs Host Disease Type of study: Guideline / Observational_studies Limits: Adult / Humans Language: En Journal: Am J Hematol Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Hematopoietic Stem Cell Transplantation / Graft vs Host Disease Type of study: Guideline / Observational_studies Limits: Adult / Humans Language: En Journal: Am J Hematol Year: 2023 Type: Article Affiliation country: United States