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Record W4417009100 · doi:10.1182/blood-2025-5183

Establishing contemporary benchmarks for Acute Myeloid Leukemia outcomes and measurable residual disease: Real-world data utilization from the ELN-david MRD international working group

2025· article· en· W4417009100 on OpenAlexaff
Gail J. Roboz, Tom Reuvekamp, Jacqueline Cloos, Malte von Bonin, Francesco Buccisano, Lukas H. Haaksma, Maura Rosane Valério Ikoma, Joana Brioso Infante, Dennis Kim, Chrysavgi Lalayanni, David de Leeuw, Josephine Anne Lucero, Francesco Mannelli, Luca Maurillo, Federico Moretti, Josep F Nomdedeu Guinot, Apostolia Papalexandri, Guillermo Ramil López, Maximilian Alexander Röhnert, Christoph Röllig, Anderson João Simione, Daniela Späth, Felicitas Thol, Anne Tierens, Adriano Venditti, François Vergez, Michael Heuser, Konstanze Döhner

Bibliographic record

VenueBlood · 2025
Typearticle
Languageen
FieldMedicine
TopicAcute Myeloid Leukemia Research
Canadian institutionsPrincess Margaret Cancer Centre
Fundersnot available
KeywordsMyeloid leukemiaClinical trialReal world dataMinimal residual diseaseLeukemiaDiseaseMyeloid

Abstract

fetched live from OpenAlex

Abstract Background The treatment landscape of acute myeloid leukemia (AML) is rapidly evolving due to advances in novel targeted agents, lower-intensity treatments, and allogeneic stem cell transplantation. Simultaneously, technologic advances are allowing increasingly sensitive detection of measurable residual disease (MRD) to guide treatment decision-making. However, our knowledge of AML patient characteristics, treatments, clinical outcomes and utility of multiparameter flow cytometry and molecular MRD techniques is primarily based on data from clinical trials. There is a need for real-world data to establish AML outcomes and MRD testing in routine practice. Thus, ELN-DAVID, an international European LeukemiaNet (ELN) working group focused on the assessment and validation of MRD in AML, launched the BENCHMARK initiative to establish a regularly updated platform for real-world clinical data and MRD assessment practices in ELN participating centers. Methods Centers provided de-identified, aggregated data from 100 or more unselected, consecutively seen patients with AML starting backwards from December 2022. Centers could include patients in clinical trials, if allowed by the clinical trial protocol. Descriptive data on patient characteristics, treatment strategies, response (morphologic and MRD) and survival were combined for collective analysis. As pooled survival analysis was not possible, the range of the median survival between centers is reported. European LeukemiaNet risk classification is defined as either the 2017 or 2022 version, depending on what the center used and entered. Results To date, data were provided for 1457 patients from 14 international centers treated between 2016 and 2022. Of these patients, 801 (55%) were male and a total of 974 (68%) patients received intensive chemotherapy, 323 (23%) non-intensive treatment, and 136 (9%) supportive care only. Across all treatment groups, most patients were not treated on clinical trials (86%), targeted (gemtuzumab-ozogamicin, FLT3 or IDH inhibitors) treatment was given to 36%, and the majority underwent allogeneic stem cell transplantation (64%). In patients treated with intensive chemotherapy the ELN risk group was 33% favorable, 29% intermediate, and 38% adverse. Of the non-intensively treated patients, most received venetoclax-based therapy (62%). Response evaluations showed complete remission (CR), or CR with incomplete count recovery (CRi) or CR with incomplete platelet recovery (CRp) in 80% of patients that were treated with intensive chemotherapy and in 54% of patients that received non-intensive treatment. Median follow-up time ranges from 4 months to 51 months and the median overall survival in each of the intensively treated ELN risk categories ranges from 16 months to not reached (NR), 8 months to NR, and 5.5 months to NR for favorable, intermediate and adverse risk patients, respectively. MRD data were available for 598 (61%) intensively treated patients after 2 cycles of treatment, 360 (37%) at the end of treatment and 295 (30%) during follow-up. Flow cytometry was the most frequently used MRD technology across all time points (cycle 2: 76%; end of treatment: 64%; follow-up: 62%), followed by quantitative PCR (cycle 2: 40%; end of treatment: 48%; follow-up: 43%). Next-generation sequencing was performed in 8% of patients after two cycles, 12% at end of treatment and 16% during follow-up. Among non-intensively treated patients, 107 (33%) had MRD data available, the majority (73%) was analyzed by flow cytometry. Conclusions The survival data from BENCHMARK-2025, reflecting international practices, are comparable to those expected from recent AML clinical trials. Most centers performed MRD assessment using flow cytometry for patients treated with intensive chemotherapy. MRD was infrequently performed in non-intensively treated patients. A standardized database has been developed to allow future analyses of individual patient data. It is anticipated that data will be updated regularly, giving the opportunity to construct synthetic control cohorts, allowing longitudinal correlation between evolving MRD practices and AML outcomes, and serving as benchmark for contemporary experience.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.066
metaresearch head score (Gemma)0.072
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.066
Threshold uncertainty score0.348

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0660.072
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0060.009
Science and technology studies0.0010.001
Scholarly communication0.0050.002
Open science0.0030.005
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.093
GPT teacher head0.362
Teacher spread0.269 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
Has abstractyes

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