医学
内科学
微小残留病
全身照射
造血干细胞移植
移植
白血病
急性淋巴细胞白血病
多元分析
年轻人
急性白血病
淋巴细胞白血病
肿瘤科
兄弟姐妹
化疗
环磷酰胺
心理学
发展心理学
作者
Jean El Cheikh,Maud Ngoya,Jacques‐Emmanuel Galimard,Péter Reményi,Alexander Kulagin,Mahmoud Aljurf,Ashrafsadat Mousavi,Depei Wu,Tülay Özçelik,Urpu Salmenniemi,Cristina Castilla‐Llorente,Gèrard Socié,Grzegorz Helbig,Thomas Schroeder,Ioanna Sakellari,Alessandro Rambaldi,Richard Burt,Alessandro Busca,Marie Balsat,Matthias Stelljes,Éolia Brissot,Sebastien Giebel,Zinaida Perić,Arnon Nagler,Ali Bazarbachi,Fabio Ciceri,Mohamad Mohty
标识
DOI:10.1038/s41409-024-02300-8
摘要
T-cell acute lymphoblastic leukemia (T-ALL) predominantly affects individuals in late childhood and young adulthood. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative modality particularly in the setting of poor risk genetics and/or persistent minimal residual disease. Limited studies have directly explored the impact of patient- and transplant-related factors on post-transplant outcomes in T-ALL. Using a large dataset from the European Society for Blood and Marrow Transplantation registry, we identified 1907 adult T-ALL patients (70% male) who underwent their first allo-HSCT in first complete remission (CR1) from matched sibling donors (MSD; 45%), unrelated donors (UD; 43%) or haploidentical donors (12%) between 2010 and 2021. The median age at transplant was 33.4 years (18.1–75). The median follow up was 2.9 years. Most patients underwent total body irradiation (TBI)-based myeloablative conditioning (69%). The 2-year overall survival (OS) was 69.4%, and leukemia -free survival (LFS) was 62.1%. In multivariate analysis, advanced age at transplant negatively affected LFS (for each 10-year increment, HR = 1.11, p = 0.004), GVHD-free, relapse-free survival (GRFS) (HR = 1.06, p = 0.04), OS (HR = 1.12, p = 0.002), and non-relapse mortality (NRM) (HR = 1.23, p < 0.001). More recent years of allo-HSCT were associated with improved GFRS (For each 3-year increment, HR = 0.89, p < 0.001), OS (HR = 0.9, p = 0.02), and decreased NRM (HR = 0.82, p = 0.008). TBI improved LFS. (HR = 0.79, p = 0.02), GRFS (HR = 0.83, p = 0.04), and relapse incidence (RI) (HR = 0.65, p < 0.001). Female-to-male transplant negatively affected GRFS (HR = 1.21, p = 0.02) and OS (HR = 1.23, p = 0.048). In vivo T-cell depletion significantly improved GFRS (HR = 0.74, p < 0.001). This large study identified prognostic factors, such as age at transplant conditioning regimen, in influencing post-transplant in adult T-ALL patients undergoing allo-HSCT. Importantly, a significant improvement over time was noted. These findings hold great promise for new adapted treatment strategies and can serve as a benchmark for future studies in that setting.