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High-dose Alemtuzumab-Cyclosporine vs Tacrolimus-Methotrexate-Sirolimus for Chronic Graft-versus-Host Disease Prevention.
Holtzman, Noa G; Curtis, Lauren M; Salit, Rachel B; Shaffer, Brian C; Pirsl, Filip; Ostojic, Alen; Steinberg, Seth M; Schulz, Eduard; Wilder, Jennifer S; Hughes, Thomas E; Rose, Jeremy; Memon, Sarfraz; Korngold, Robert; Gea-Banacloche, Juan; Fowler, Daniel H; Hakim, Frances T; Gress, Ronald E; Bishop, Michael R; Pavletic, Steven Z.
Afiliação
  • Holtzman NG; National Cancer Institute, Center for Cancer Research, Bethesda, Maryland, United States.
  • Curtis LM; Ascension Maryland Saint Agnes Hospital, United States.
  • Salit RB; National Cancer Institute, National Institutes of Health, United States.
  • Shaffer BC; National Cancer Institute, National Institutes of Health, United States.
  • Pirsl F; National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States.
  • Ostojic A; National Cancer Institute, Center for Cancer Research, Bethesda, Maryland, United States.
  • Steinberg SM; Biostatistics and Data Management Section, National Cancer Institute, NIH, Bethesda, Maryland, United States.
  • Schulz E; Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States.
  • Wilder JS; National Institutes of Health, Bethesda, Maryland, United States.
  • Hughes TE; National Institutes of Health, Bethesda, Maryland, United States.
  • Rose J; NCI, Bethesda, Maryland, United States.
  • Memon S; National Institutes of Health, Bethesda, Maryland, United States.
  • Korngold R; Hackensack Meridian Health, Nutley, New Jersey, United States.
  • Gea-Banacloche J; National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States.
  • Fowler DH; Rapa Therapeutics, United States.
  • Hakim FT; National Cancer Institute, Bethesda, Maryland, United States.
  • Gress RE; National Cancer Institute, Bethesda, Maryland, United States.
  • Bishop MR; The David and Etta Jonas Center for Cellular Therapy, University of Chicago, Chicago, Illinois, United States.
  • Pavletic SZ; National Cancer Institute, Bethesda, Maryland, United States.
Blood Adv ; 2024 Apr 26.
Article em En | MEDLINE | ID: mdl-38669315
ABSTRACT
Chronic graft-versus-host disease (cGVHD) remains a significant problem for patients after allogeneic hematopoietic stem cell transplants (allo-HSCT). While in vivo lymphodepletion by antibodies for cGVHD prophylaxis has been explored in the myeloablative setting, its effects after reduced intensity conditioning (RIC) are not well described. Patients (n=83) with hematologic malignancies underwent targeted lymphodepletion chemotherapy followed by a RIC allo-HSCT using peripheral blood stem cells from unrelated donors. Patients were randomized to two GVHD prophylaxis arms high-dose alemtuzumab/cyclosporine (AC, n=44) and tacrolimus/methotrexate/sirolimus (TMS, n=39) with the primary endpoint of cumulative incidence of severe cGVHD. The incidence of severe cGVHD was lower with AC vs TMS prophylaxis at 1- and 5-years (0% vs 10.3% and 4.5% vs 28.5%, overall p=0.0002), as well as any grade (p=0.003) and moderate-severe (p<0.0001) cGVHD. AC was associated with higher rates of grade III-IV infections (p=0.02) and relapse (52% vs 21%, p=0.003) with a shorter 5-year PFS (18% vs 41%, p=0.01) and no difference in 5-year GRFS, OS, or NRM. AC severely depleted naïve T-cells reconstitution, resulting in reduced TCR repertoire diversity, smaller populations of CD4 Treg and CD8 Tscm, but a higher ratio of Treg to naïve T-cells at 6 months. In summary, an alemtuzumab-based regimen successfully reduced the rate and severity of cGVHD after RIC allo-HSCT and resulted in a distinct immunomodulatory profile which may have reduced cGVHD incidence and severity. However, increased infections and relapse resulted in a lack of survival benefit after long-term follow-up. ClinicalTrials.gov identifier NCT00520130.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article