TBI/Cy followed by auto-HSCT is a good choice next to allo-HSCT for patients with T-LBL/ALL.
Autor: | Mao J; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Ge J; Department of Oncology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Ding S; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Sun Z; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Nan F; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Yu H; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Ding J; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Wang X; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Liu Z; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China., Zhang M; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China. mingzhi_zhang1@163.com., Fu X; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China. zymfxr_2006@126.com. |
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Jazyk: | angličtina |
Zdroj: | Scientific reports [Sci Rep] 2024 Sep 27; Vol. 14 (1), pp. 22356. Date of Electronic Publication: 2024 Sep 27. |
DOI: | 10.1038/s41598-024-72897-9 |
Abstrakt: | The aim of this retrospective study was to evaluate the efficiency and safety of total body irradiation plus cyclophosphamide (TBI/Cy) followed by autogenetic hematopoietic stem cell transplantation (auto-HSCT) in T-LBL/ALL patients that cannot receive allogeneic hematopoietic stem cell transplant (allo-HSCT). Between 2013 and 2023, 24 patients received auto-HSCT following by TBI/Cy, 26 patients underwent allo-HSCT, all patients achieved completed hematopoietic reconstitution after HSCT. The progression free survival (PFS) and overall survival (OS) had no statistically significant differences between the two groups (P = 0.791, HR 1.127, 95%CI 0.456-2.785; P = 0.456, HR 0.685, 95%CI 0.256-1.828). Although the cumulative incidence of relapse was lower for patients who received allo-HSCT than auto-HSCT (P = 0.033, HR 3.707, 95%CI 1.188-11.570, 2-year relapse 11.5% vs. 33.3%), the incidence of non-relapse mortality (NRM) was higher than that in the auto-HSCT group (P = 0.014, HR 0.000, 95%CI -1.000 - -1.000, 2-year NRM, 23.1% vs. 0%). Trough Landmark analysis, the two groups showed a statistically significant difference in 3-year PFS and 4-year OS curves (Figure S2A&B, P = 0.039, HR 0.426, 95%CI 0.163-1.117; P = 0.014, HR 0.317, 95%CI 0.113-0.887). By COX analysis, poor baseline performance status (ECOG-PS ≥ 2) and CNS involvement were risk factors for PFS and OS. In conclusion, TBI/Cy followed by auto-HSCT is a good choice next to allo-HSCT for patients with T-LBL/ALL. (© 2024. The Author(s).) |
Databáze: | MEDLINE |
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