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Record W4379979778 · doi:10.1002/hon.3166_ot15

PHASE 1 STUDY OF PRT1419 (MCL1 INHIBITOR) AS MONOTHERAPY OR IN COMBINATION WITH AZACITIDINE OR VENETOCLAX IN PATIENTS WITH RELAPSED/REFRACTORY MYELOID OR B‐CELL MALIGNANCIES

2023· article· en· W4379979778 on OpenAlexaffabout
R. R. Zuniga, S. Nair, Gina Keiffer, Farhad Ravandi‐Kashani, Aaron D. Goldberg, Elie Traer, Lukas P. Frenzel, Christoph Röllig, Gina Savickas, Wei‐Zen Sun, Sukhreet Atwal, Wan‐Jen Hong, Sarit Assouline

Bibliographic record

VenueHematological Oncology · 2023
Typearticle
Languageen
FieldMedicine
TopicAcute Myeloid Leukemia Research
Canadian institutionsMcGill UniversityJewish General Hospital
FundersUniversitat Autònoma de Barcelona
KeywordsVenetoclaxMedicineAzacitidineTolerabilityInternal medicineMyeloid leukemiaOncologyMyeloidVenRituximabLymphomaCancer researchLeukemiaChronic lymphocytic leukemiaAdverse effectBiology

Abstract

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Introduction: PRT1419 is a potent and selective inhibitor of myeloid cell leukemia-1 (MCL-1). MCL-1 is frequently amplified or overexpressed in hematologic malignancies and is associated with higher grade malignancy and poor prognosis (Xiang et al., Onco Targets Ther 2018). Azacitidine (AZA) treatment was shown to induce several proapoptotic changes in primary acute myeloid leukemia (AML) isolates, including a decrease in MCL-1 protein levels (Tsao et al, Ann Hematol 2012; Jin et al, Clin Cancer Res 2020). Several mechanisms of primary and acquired resistance have been described in patients (pts) with AML treated with venetoclax (VEN)-based regimens, including the loss of dependence on BCL-2 and upregulation of MCL-1 (Saliba et al., Cancer Drug Resist 2021; Pei et al., Cancer Discov 2020). Considering that MCL-1 upregulation is a mediator of VEN resistance and AZA downregulates MCL-1, PRT1419 may confer additive or synergistic benefits to AZA or VEN in treatment-resistant myeloid or B-cell malignancies. Methods: PRT1419-03 is a phase 1, open-label, multicenter, dose-finding study to evaluate the safety, tolerability, recommended phase 2 dose (R2PD), and preliminary efficacy of PRT1419 as monotherapy or in combination with AZA or VEN in pts with selected relapsed/refractory myeloid or B-cell malignancies. Pts must have progressed on prior treatment without access to, or eligibility for, further approved therapies. Adult pts with confirmed diagnosis of AML, CMML, MDS, MDS/MPN Overlap Syndrome, CLL/SLL, or B-cell NHLs (mantle cell lymphoma, follicular lymphoma, marginal zone lymphoma) are eligible for this study. Other key eligibility criteria include Eastern Cooperative Oncology Group performance status of 0 to 2 and adequate organ and cardiac function as assessed by echocardiogram or biochemical markers of cardiac damage. As monotherapy, pts will receive escalating doses of intravenous PRT1419 once weekly in a 28-day cycle using a 3 + 3 dose escalation design until a maximum tolerated dose (MTD) or RP2D dose has been reached. Once the RP2D for monotherapy has been defined, pts will receive escalating doses of PRT1419 in combination with AZA (myeloid malignancies) or VEN (myeloid malignancies; B-cell malignancies) until MTD/RP2D is reached. Pts will then be enrolled into indication-specific dose confirmation cohorts. PRT1419 treatment will continue until relapse/disease progression, intolerance, or pt withdrawal. The primary endpoints include safety, tolerability, dose-limiting toxicities (DLTs), and RP2D of PRT1419 as monotherapy. Secondary endpoints include safety, tolerability, DLTs, RP2D for PRT1419 in combination The research was funded by: Prelude Therapeutics Keywords: combination therapies, molecular targeted therapies, ongoing trials Conflicts of interests pertinent to the abstract. R. R. Zuniga Employment or leadership position: New York Cancer & Blood Specialist - Port Jefferson Station, NY Consultant or advisory role Mirati G. Keiffer Consultant or advisory role Astellas Honoraria: Astellas Research funding: AbbVie, Prelude Therapeutics, Cyteir Therapeutics F. Ravandi-Kashani Consultant or advisory role BMS/celgene, Novartis, Astellas, Abbvie, Jazz, Taiho, Syros Honoraria: BMS/celgene, Novartis, Astellas, Abbvie, Jazz, Taiho, Syros Research funding: Amgen, Abbvie, Astex, Prelude, Biomea A. D. Goldberg Consultant or advisory role AbbVie, Daiichi Sankyo, Astellas, and Genentech Honoraria: Dava Oncology Research funding: AbbVie, Aptose, Daiichi Sankyo, Celularity, ADC Therapeutics, Aprea, AROG, Pfizer, Prelude, and Trillium E. Traer Consultant or advisory role Abbvie, Astellas, Daiichi-Sankyo, Servier Research funding: Prelude Therapeutics, Schrodinger, Incyte, Astra-Zeneca Other remuneration: Patents, Royalties: Humarrow, Inc L. P. Frenzel Consultant or advisory role Abbvie Educational grants: Abbvie C. Röllig Consultant or advisory role AbbVie, Astellas, BMS, Jazz, Novartis, Pfizer, Servier Honoraria: AbbVie, Astellas, BMS, Jazz, Novartis, Pfizer, Servier Research funding: AbbVie, Novartis, Pfizer W. Sun Honoraria: Prelude S. K. Atwal Employment or leadership position: Prelude Therapeutics Stock ownership: Prelude Therapeutics W. Hong Employment or leadership position: Prelude Therapeutics, Imago BioSciences, Genentech Consultant or advisory role Imago BioSciences Stock ownership: Imago BioSciences Other remuneration: Patents, Royalties: Stanford University S. E. Assouline Consultant or advisory role AbbVie, BMS, AstraZeneca, Janssen, BeiGene, Pfizer, Roche Research funding: Novartis Canada

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.352
Threshold uncertainty score0.693

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.002
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0000.000

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 head0.040
GPT teacher head0.348
Teacher spread0.308 · 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 teacher head, 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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Citations2
Published2023
Admission routes2
Has abstractyes

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