Autor: |
Asensi Cantó, P., Gómez-Seguí, I., Montoro, J., Villalba Montaner, M., Chorão, P., Solves Alcaína, P., Santiago Balsera, M., Lloret Madrid, P., Solís Ruiz, J., Sopeña Pell-Ilderton, C., Martínez Campuzano, D., Granados Serrano, P., Eiris del Río, J., Louro, A., Rebollar, P., Perla, A., Benavente, R., De la Rubia Comos, J., Sanz, M. A., Balaguer, A., Sanz, J. |
Zdroj: |
Bone Marrow Transplantation; November 2024, Vol. 59 Issue: 11 p1577-1584, 8p |
Abstrakt: |
Posttransplant cyclophosphamide, sirolimus and mycophenolate mofetil (PTCy/siro/MMF) constitutes an innovative and well-tolerated acute graft-versus-host disease (aGVHD) prophylaxis after allogeneic stem cell transplantation (allo-HSCT), but risk factors for aGVHD incidence and therapy failure in this setting are scarce. This study prospectively registered all consecutive adult patients with hematologic malignancies who received a myeloablative allo-HSCT using PTCy/siro/MMF prophylaxis at our institution between 2017 and 2023. A total of 385 patients were included, of whom 44%, 34% and 22% were transplanted from matched sibiling, matched unrelated and haploidentical donors, respectively. The 180-day cumulative incidence of aGVHD was 21% (95% confidence interval [CI] 17–25%) for grade II–IV and 11% (95% CI 8–14%) grade III–IV aGVHD. The use of haploidentical donors was associated with an increased risk of severe aGVHD. Among 75 patients receiving first-line systemic corticosteroids, 49% achieved a sustained complete response, while 23% and 24% developed steroid-dependent (SD-aGVHD) and steroid-refractory aGVHD (SR-aGVHD), respectively. SR-aGVHD was associated with worse salvage treatment response and overall survival compared to SD-aGVHD. The 1-year cumulative incidence of aGVHD-related mortality was 5.4% (95% CI, 3.3–8.1). Risk factors for aGVHD-related mortality included haploidentical donors, older donors, diagnosis of myeldysplastic neoplasms, and grade IV aGVHD. This study confirms a low incidence aGVHD with PTCy/siro/MMF prophylaxis. SR-aGVHD showed poorer response to salvage therapies and worse survival, while haploidentical donors and older donor age were negative predictors for aGVHD-related deaths. |
Databáze: |
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