Related Experiment Video
Updated: Dec 11, 2025

Flow Cytometry to Estimate Leukemia Stem Cells in Primary Acute Myeloid Leukemia and in Patient-derived-xenografts, at Diagnosis and Follow Up
Published on: March 26, 2018
Prognostic impact of the ELN2017 risk classification in patients with AML receiving allogeneic transplantation
Juliane Grimm1, Madlen Jentzsch1, Marius Bill1
1Medical Clinic and Policlinic 1, Hematology and Cellular Therapy, Leipzig University Hospital, Leipzig, Germany.
Insights
The European LeukemiaNet 2017 (ELN) risk classification effectively predicts outcomes for acute myeloid leukemia (AML) patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT), identifying high-risk groups. This classification retains prognostic value post-transplant.
Area of Science:
- Hematology
- Oncology
- Stem Cell Transplantation
Background:
- The 2017 European LeukemiaNet (ELN) classification stratifies acute myeloid leukemia (AML) patients into risk groups based on cytogenetic and molecular markers.
- Prognostic significance of the ELN 2017 classification specifically after allogeneic hematopoietic stem cell transplantation (HSCT) remains understudied.
Purpose of the Study:
- To evaluate the prognostic impact of the ELN 2017 risk classification in AML patients undergoing allogeneic HSCT.
- To assess the role of specific genetic aberrations (TP53 mutations, monosomal karyotype) and measurable residual disease (MRD) in this context.
Main Methods:
- Risk stratification of 234 AML patients undergoing allogeneic HSCT using the ELN 2017 criteria.
- Analysis of prognostic significance, relapse rates, and overall survival based on ELN 2017 risk groups.
- Subgroup analyses for TP53 mutations, monosomal karyotype, and pre-HSCT MRD status (assessed by digital droplet PCR).
Main Results:
- The ELN 2017 classification significantly stratified patients into favorable, intermediate, and adverse risk groups with distinct prognoses post-HSCT.
- Patients with monosomal karyotype or TP53 mutations showed increased relapse rates, even within the adverse-risk group.
- Measurable residual disease (MRD) positivity before HSCT was associated with impaired prognosis, similar to the ELN 2017 adverse risk group.
Conclusions:
- The ELN 2017 classification retains prognostic value in AML patients undergoing allogeneic HSCT.
- TP53 mutations, monosomal karyotype, and pre-HSCT MRD positivity indicate a particularly dismal prognosis, underscoring the need for intensified monitoring and treatment strategies.
Abstract:
In 2017, an updated European LeukemiaNet (ELN) risk classification was published allocating patients with acute myeloid leukemia (AML) to 3 risk groups on the basis of certain cytogenetic and molecular aberrations. To date, studies of the prognostic significance of the ELN2017 risk classification in the context of an allogeneic hematopoietic stem cell transplantation (HSCT) are lacking. We performed risk stratification according to the ELN2017 classification in 234 patients with AML who underwent allogeneic HSCT as a consolidation therapy. In our cohort, the risk of 39.7% of the patients was classified as favorable, that of 12.8% as intermediate, and that of 47.4% as adverse. In the context of allogeneic HSCT, the assignment to the 3 ELN2017 risk groups retained its prognostic significance, with patients with favorable risk having the best prognosis and those with adverse risk having the worst one. Subgroup analyses showed that patients with a monosomal karyotype or TP53 mutation had considerably increased relapse rates, even in the adverse-risk group. When we analyzed the impact of digital droplet PCR-based measurable residual disease (MRD) before allogeneic HSCT, MRD+ patients had impaired prognoses, with cumulative incidence of relapse and overall survival comparable to those of patients classified as having an ELN2017 adverse genetic risk. This study is the first to demonstrate that the ELN2017 classification distinguishes the 3 risk groups with significantly distinct prognoses, even after allogeneic HSCT, and emphasizes the dismal prognosis of patients with AML with TP53 mutations, monosomal karyotype, or MRD positivity after allogeneic HSCT.
More Related Videos
07:38Intracellular Phosphoflow Cytometry of Acute Myeloid Leukemia Patient-Derived Xenotransplants
Published on: June 6, 2025
09:57Comprehensive Protocol to Sample and Process Bone Marrow for Measuring Measurable Residual Disease and Leukemic Stem Cells in Acute Myeloid Leukemia
Published on: March 5, 2018