Post-transplant cyclophosphamide compared to sirolimus/tacrolimus in reduced intensity conditioning transplants for patients with lymphoid malignancies.
Maria Laura FoxGarcía-Cadenas IreneVictor NavarroAriadna Pérez MartínezMeriem KaraIrene Sánchez BazánChristelle Ferra CollRebeca Bailen AlmoroxLeyre BentoRocío ParodyAlbert EsquirolGuillermo OrtíAlberto MussettiOlga SalameroRodrigo Martino BofarullAna Pérez GonzálezPere BarbaMi KwonCarlos SolanoFrancesc BoschDavid Valcarcelnull nullPublished in: Bone marrow transplantation (2024)
Despite novel cellular and immunomodulatory therapies, allogeneic hematopoietic stem cell transplantation (HSCT) remains a treatment option for lymphoid malignancies. Post-transplant cyclophosphamide (PTCY) is increasingly employed for graft vs. host disease (GVHD) prophylaxis. This study aims to evaluate the safety and efficacy of PTCY in reduce intensity (RIC) HSCT for patients with lymphoid neoplasms compared to sirolimus with tacrolimus (SIR/TAC). The primary endpoint was to compare grade III-IV acute GVHD, severe chronic GVHD, and relapse-free survival (GRFS) between the two GVHD prophylaxis strategies. This study, conducted from January 2012 to December 2020, included 171 consecutive patients (82 in the PTCY and 89 in the SIR/TAC group). Results revealed a significantly decreased incidence of moderate and severe forms of chronic GVHD in PTCY cohort (5.8% [95% CI, 1.8 to 13.1]) versus the SIR/TAC cohort (39.6% [95% CI, 29.3 to 49.7] (p < 0.001)). Other outcomes, including GRFS (PTCY [45.9% (95% CI, 35.8-58.7)] and SIR/TAC groups [36.8% (95% CI, 28-48.4)], (p = 0.72)), non-relapse mortality (NRM), relapse and overall survival (OS) were similar in both groups. Interestingly, the failure to achieve GRFS was mainly attributed to GVHD in the SIR/TAC group, while disease relapse was the primary reason in the PTCY cohort.
Keyphrases
- allogeneic hematopoietic stem cell transplantation
- free survival
- acute myeloid leukemia
- acute lymphoblastic leukemia
- high intensity
- drug induced
- low dose
- end stage renal disease
- high dose
- ejection fraction
- chronic kidney disease
- early onset
- newly diagnosed
- type diabetes
- liver failure
- coronary artery disease
- adipose tissue
- hepatitis b virus
- cardiovascular events
- single cell
- skeletal muscle
- insulin resistance
- mechanical ventilation
- glycemic control