MicroabstractAML and MDS relapse is the most frequent cause of allo-SCT failure. This subanalysis of the GITMO AML/MDS relapse study focuses on 647 AML/MDS relapses that were treated with either HMAs-based therapy (n = 308) or other treatments (n = 339), including intensive chemotherapy, FLT3-inhibitors, and second allo-SCT. The ORR with or without HMA-based salvage treatment was 33% versus 40%, respectively (P = .006). The long-term OS and TRM of the two groups were superimposable. Independently from the type of salvage, an advantage in OS was observed when DLI was included (P < .001). Relapse within 12 months after SCT, low disease burden at relapse, and the CR status at transplant confirmed their independent strong prognostic impact on both HMA and non-HMA-based group (HR 0.05, 0.44, 0.49 and HR 0.19, 0.32, 0.53, respectively).Despite the lower ORR observed with HMA-based therapy, the long-term OS was comparable to that observed with other therapies. The immune control of the disease relapse with DLI is of benefit, independently from the salvage therapy

Treatment of Acute Myeloid Leukemias and Myelodisplastic Syndromes Relapsing After Allogeneic Stem Cell Transplantation: An In-Depth Analysis of the GITMO AML/MDS-Relapse Registry Study

Patriarca F.;
2026-01-01

Abstract

MicroabstractAML and MDS relapse is the most frequent cause of allo-SCT failure. This subanalysis of the GITMO AML/MDS relapse study focuses on 647 AML/MDS relapses that were treated with either HMAs-based therapy (n = 308) or other treatments (n = 339), including intensive chemotherapy, FLT3-inhibitors, and second allo-SCT. The ORR with or without HMA-based salvage treatment was 33% versus 40%, respectively (P = .006). The long-term OS and TRM of the two groups were superimposable. Independently from the type of salvage, an advantage in OS was observed when DLI was included (P < .001). Relapse within 12 months after SCT, low disease burden at relapse, and the CR status at transplant confirmed their independent strong prognostic impact on both HMA and non-HMA-based group (HR 0.05, 0.44, 0.49 and HR 0.19, 0.32, 0.53, respectively).Despite the lower ORR observed with HMA-based therapy, the long-term OS was comparable to that observed with other therapies. The immune control of the disease relapse with DLI is of benefit, independently from the salvage therapy
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11390/1329247
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