Use ultra-sensitive residual-disease tests after induction to decide who really needs a transplant, sparing the rest its risks.
The idea is to use ultra-sensitive residual disease tests, NPM1 qPCR or error-corrected NGS, after two cycles of induction to decide which intermediate-risk acute myeloid leukaemia patients really need an allogeneic transplant. MRD status is the strongest predictor of relapse, transplant carries substantial risk, and its benefit concentrates in MRD-positive patients; ELN 2022 already recommends transplant for them, but randomised confirmation is lacking. The hypothesis is that MRD-negative patients can receive chemotherapy consolidation instead with equal overall survival and less toxicity. The test randomises MRD-negative patients to transplant or consolidation with MRD surveillance; myeloMATCH, HOVON and AMLSG trials already stratify by MRD, so it is being tested at scale.
Shares ELN 2022 risk classification, Acute myeloid leukaemia.
Shares Allogeneic stem cell transplantation, Acute myeloid leukaemia.
Shares MRD-negative complete remission, NGS-based MRD (clonoSEQ and molecular MRD), Allogeneic stem cell transplantation.
Shares Allogeneic stem cell transplantation, Acute myeloid leukaemia.
Shares Allogeneic stem cell transplantation, Acute myeloid leukaemia.
Shares Allogeneic stem cell transplantation, Acute myeloid leukaemia.
Shares Allogeneic stem cell transplantation, Acute myeloid leukaemia.
Shares Allogeneic stem cell transplantation, Acute myeloid leukaemia.