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A phase 2 study of olutasidenib in relapsed/refractory acute myeloid leukemia: Outcomes by number of prior treatment regimens.

2025· article· en· W4410809345 on OpenAlexaff
Eunice S. Wang, Jörge E. Cortes, Andrew H. Wei, Stéphane de Botton, Antonio Curti, Pau Montesinos, Karen Yee, Joseph G. Jurcic, William B. Donnellan, Jay Yang, Brian A. Jonas, Aaron Sheppard, Hua Tian, Justin M. Watts

Bibliographic record

VenueJournal of Clinical Oncology · 2025
Typearticle
Languageen
FieldMedicine
TopicChronic Myeloid Leukemia Treatments
Canadian institutionsPrincess Margaret Cancer CentreUniversity Health Network
Fundersnot available
KeywordsMedicineRefractory (planetary science)Myeloid leukemiaOncologyInternal medicine

Abstract

fetched live from OpenAlex

6545 Background: A subset of patients (7-14%) with acute myeloid leukemia (AML) have mutations in the isocitrate dehydrogenase 1 gene (m IDH1 ). Olutasidenib (OLU), a selective, potent, oral inhibitor of mIDH1, is approved for treatment of relapsed/refractory (R/R) m IDH1 AML. Results from the phase 2 pivotal cohort (NCT02719574) demonstrated clinical efficacy and tolerability of OLU, with a complete remission/complete remission with partial hematological recovery (CR/CRh) rate of 35% for a median duration of 25.9 months. Here we evaluated the efficacy and safety of OLU in patients with R/R AML grouped by the number of prior regimens. Methods: The pivotal cohort of the phase 2 study assessed OLU 150 mg BID in adult patients and included efficacy endpoints of CR/CRh, overall response rate (ORR), duration of response (DOR), and overall survival (OS). This post hoc analysis evaluated outcomes based on when patients received OLU: after 1-2 or ≥3 prior lines of therapy. Results: There were 147 patients in the efficacy evaluable analysis set (1-2 prior regimens, n=93; ≥3 prior regimens, n=54). Median age was 72 years in patients with 1-2 prior regimens and 66.5 years in those with ≥3 prior regimens. Forty-three percent and 33% of patients had prior treatment with a hypomethylating agent, and 11% and 4% received prior venetoclax therapy (1-2 and ≥3 prior regimens groups, respectively). In patients with ≥3 prior regimens, 31% had prior hematopoietic stem cell transplantation vs none in those with 1-2 prior regimens. Those in the 1-2 prior regimens group had a higher ORR and CR/CRh rate and longer median OS, with a larger percentage of patients achieving CR, than those in the ≥3 prior regimens group (Table 1). All patients experienced ≥1 treatment-emergent adverse event (TEAE). Serious TEAEs were reported in 73% (68/93) and 77.8% (42/54) of patients in the 1-2 and ≥3 prior regimens groups, respectively, and TEAEs ≥grade 3 occurred in 89.2% (83/93) and 90.7% (49/54). The most common TEAEs included nausea, decreased red blood cell count, and fatigue. No new safety signals were identified. Conclusions: Higher response rates (including CR and CRh) and greater survival were observed in patients receiving OLU following 1-2 versus ≥3 prior treatment regimens, providing rationale for initiating OLU earlier in the R/R treatment paradigm. Clinical trial information: NCT02719574 . Efficacy of OLU stratified by number of prior regimens. 1-2 Prior Regimensn=93 ≥3 Prior Regimensn=54 ORR, n (%); 95% CI 50 (54); 43.1, 64.2 21 (39); 25.9, 53.1 DOR, median months (95% CI) 14.8 (7.4, 25.9) 16.6 (5.8, NR) CR rate, n (%); 95% CI 35 (38); (27.8, 48.3) 12 (22); (12.0, 35.6) DOR, median months (95% CI) 21.3 (12.0, NR) NR (8.7, NR) CR/CRh rate, n (%); 95% CI 38 (41); 30.8, 51.5 13 (24); 13.5, 37.6 DOR, median months (95% CI) 25.3 (12.0, NR) NR (8.7, NR) OS, median months (95% CI) 13.0 (9.3, 18.9) 8.9 (5.8, 14.9) NR, not reached.

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)0.003
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: Non-randomized trial · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.014

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0030.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.002
Bibliometrics0.0010.000
Science and technology studies0.0000.001
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0030.001

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 head0.065
GPT teacher head0.478
Teacher spread0.413 · 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 designNon-randomized trial
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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