INTRODUCTION: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment for hematologic malignancies. Serum ferritin, an indicator of iron overload and systemic inflammation, has been suggested as a prognostic biomarker for post-transplant outcomes. The association between pre-transplant serum ferritin levels and post-transplant outcomes, particularly 100-day transplant-related mortality (TRM), was evaluated in acute leukemia patients who underwent their first allo-HSCT.
METHODS: We conducted a retrospective analysis of 170 adult patients with acute leukemia who received their initial myeloablative allo-HSCT during complete remission from 2015 to 2021 at a single institution. Patients were divided into two groups based on their ferritin levels before the transplant: <1500 µg/L and ≥1500 µg/L. The primary endpoint was 100-day TRM.
RESULTS: The mean age of the cohort was 39 years, and 60.6% had acute myeloid leukemia. The median level of ferritin was 1595 µg/L. The high-ferritin group exhibited significantly higher 100-day mortality (10.8% vs. 1.3%, p = 0.013) and 100-day TRM (8.6% vs. 1.3%, p = 0.041) than the low-ferritin group. Invasive fungal infections were more frequent in the high-ferritin group (11.8% vs. 3.9%, p=0.091). There were no notable differences in engraftment kinetics, cytomegalovirus reactivation, or graft-versus-host disease rates between the two groups.
DISCUSSION AND CONCLUSION: High pre-transplant serum ferritin correlates with elevated early TRM and a tendency toward increased rates of invasive fungal infections post-allo-HSCT. Ferritin may be used as a simple and accessible biomarker for initial risk stratification, facilitating enhanced infectious monitoring and possible iron-reducing interventions in high-risk patients. Future multicenter studies are necessary to confirm these results.
Keywords: ferritin, allogeneic stem cell transplantation, acute leukemia, transplant-related mortality, invasive fungal infection