MétaCan
Menu
← Back to cohort

Low-Level FLT3-ITD Mutations Do Not Predict for Higher Relapse Rate in AML with Standard Risk Karyotpye.

2009· article· en· W2588572219 on OpenAlexaff
Richard Ward, Suzanne Kamel‐Reid, Wei Xu, Mark D. Minden, Aaron D. Schimmer, Karen Yee, Andre C. Schuh, Vikas Gupta, Joseph Brandwein

Bibliographic record

VenueBlood · 2009
Typearticle
Languageen
FieldMedicine
TopicAcute Myeloid Leukemia Research
Canadian institutionsUniversity Health NetworkPrincess Margaret Cancer CentreOntario Institute for Cancer Research
Fundersnot available
KeywordsCytarabineMedicineInternal medicineGastroenterologyChemotherapy regimenChemotherapyDaunorubicinOncologySurgery

Abstract

fetched live from OpenAlex

Abstract Abstract 1591 Poster Board I-617 High-level FLT3-ITD mutations predict for a higher relapse rate and inferior survival among patients with standard risk karyotype AML. The influence of low-level FLT3-ITD mutations is less clear, although the MRC group (Gale et al, 2008) reported that low-level mutations are associated with an inferior prognosis as compared to an unmutated group. In the absence of FLT3-ITD, NPM1 mutations predict for a lower relapse rate. We analyzed outcomes of intensive chemotherapy in patients with standard risk karyotype AML (n=131) between 2004-2008. Patients received uniform induction chemotherapy consisting of cytarabine plus daunorubicin (7+3), followed by 2 consolidations consisting of high-dose cytarabine plus daunorubicin for pts under age 60 (n=96) or 7+3 followed by NOVE for pts age 60+ (n=35). Patients were divided into 3 groups based on the ratio of FLT3-ITD:FLT3-wt: There were 73 patients with negative FLT3-ITD (defined as FLT3-ITD:wt ratio < 0.01), 30 patients with low-level ITD (ratio > 0.01 – 0.37), and 28 patients with high-level ITD (ratio > 0.37). The mean presenting WBC was 32.2 ×109/L in the group with negative ITD, 49.4 ×109/L in the group with low-level ITD and 97.2 ×109/L in the group with high-level ITD (p < 0.0001). At a median follow-up of 19 months (range 2-95 months), the median OS of the entire group was 21.3 months. Patients with high-level ITD had a significantly inferior RFS (p = 0.0009) and OS (p = 0.003) as compared to the low-level and negative groups. Comparing the negative ITD and low-level ITD groups, there was no significant difference in RFS (p = 0.65) or OS (p = 0.18). The frequency of NPM1 mutations was not significantly different between these two groups (42% vs. 35%). These data were re-analyzed using a different cutoff according to % FLT-ITD positivity: negative < 1% (n=73), low-level 1 – 50% (n=42), high level > 50% (n=16). Using these ranges, the low-level FLT3-ITD group had a significantly lower CR rate (74% vs. 93%, p = 0.004) and OS (36% vs. 61%, p = 0.01) as compared to the group with negative FLT3-ITD, but there was no significant difference between these two groups with respect to RFS (2 year RFS 48% in low-level ITD group vs. 40% in negative ITD group). The high-level ITD group demonstrated significantly inferior RFS (p = 0.02) and OS (p = 0.01) as compared to the other two groups. These findings confirm the poor prognosis associated with high-level FLT3-ITD mutations due to high relapse rates. However, in contrast to previously reported data, we did not find that low level FLT3 –ITD mutations were associated with inferior RFS, although we did find, unexpectedly, that this low-level group had a lower CR rate. Disclosures No relevant conflicts of interest to declare.

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)0.000
metaresearch head score (Gemma)0.001
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 score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.020
GPT teacher head0.288
Teacher spread0.267 · 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".

Quick stats

Citations0
Published2009
Admission routes1
Has abstractyes

Explore more

Same venueBlood→Same topicAcute Myeloid Leukemia Research→French-language works237,207→