4.2 Article

Allogeneic Hematopoietic Cell Transplantation in the Outpatient Setting

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 25, Issue 11, Pages 2152-2159

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2019.06.025

Keywords

Allogeneic hematopoietic cell transplantation; Nonmyeloablative conditioning; Survival; Prognostic factors; Hospitalizations

Funding

  1. National Institutes of Health (NIH) [P01 CA078902, P01 HL036444, P01 CA018029, P30 CA015704, T32 HL007093]
  2. Laura Landro Solomon Endowment Fund
  3. Gabrielle's Angel Foundation for Cancer Research
  4. NIH, Bethesda, Maryland

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Conditioning with fludarabine and low-dose total-body irradiation before allogeneic hematopoietic cell transplantation (HCT) enabled treating older or medically infirm patients with advanced hematologic malignancies in the outpatient setting. Between December 1997 and June 2017, 1037 patients with hematologic malignancies received peripheral blood stem cell (PBSC) grafts from HLA-matched or 1 HLA antigen/allele-mismatched related or unrelated donors. Median age was 58 (range, 18 to 80) years. Serious comorbidities with Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) scores >= 3 were present in 52% of patients. We found that 47% of patients were either never hospitalized or only had an overnight hospital stay for infusion of late-arriving PBSCs while 53% were admitted for a median of 6 days. Main reasons for admission were infection, fever, graft-versus-host disease, and regimen-related toxicity. Two thirds of admissions occurred within 3 weeks of KT. The 5-year risk of nonrelapse mortality (NRM) was 26% among hospitalized patients and 13% among nonhospitalized patients. Significant risk factors for hospitalization included unrelated transplants, 1 HLA antigen-mismatched transplant, high HCT-CI scores, and diagnosis of nonmyeloma malignancies. Significant risk factors for NRM were hospitalization, older age, unrelated transplants, and high HCT-CI scores. Ambulatory allogeneic HCT is feasible and safe. (C) 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.

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