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Record W4405051335 · doi:10.1182/blood-2024-203473

Canadian Real-World Data for Acute Myeloid Leukemia Chemotherapy-Ineligible Patients on Venetoclax: An Interim Analysis from the Prospective Liven Study

2024· article· en· W4405051335 on OpenAlexaffabout
Kristjan Paulson, Thomas Dunne, Lalit Saini, Nicole Laferriere, Michelle Geddes, Stephanie Desilets, David Sanford, Leanne Genge, Paola Lembo, Pierre‐André Fournier, Brian Leber

Bibliographic record

VenueBlood · 2024
Typearticle
Languageen
FieldMedicine
TopicAcute Myeloid Leukemia Research
Canadian institutionsMcMaster UniversityJuravinski Cancer CentreBC Cancer AgencyUniversity of British ColumbiaBaker Hughes (Canada)Vancouver General HospitalUniversity of CalgaryMemorial University of NewfoundlandThunder Bay Regional Research InstituteUniversité de SherbrookeLondon Health Sciences CentreCancerCare Manitoba
Fundersnot available
KeywordsVenetoclaxMedicineInternal medicineInterim analysisCytarabineChemotherapy regimenRegimenMyeloid leukemiaInduction chemotherapyOncologyPediatricsLeukemiaClinical trialChemotherapyChronic lymphocytic leukemia

Abstract

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Introduction: Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults and has the lowest survival rate. Recent advances in AML therapies have led to improvements in patient outcomes. The objective of the prospective observational LIVEN study is to assess real-world clinical outcomes in Canadian patients with AML who are ineligible for intensive induction chemotherapy and treated first-line with venetoclax combination therapy with azacitidine [AZA] or low-dose cytarabine [LDAC] in inpatient and outpatient settings. Methods: Adults ≥ 18 years diagnosed with AML were enrolled following the decision to treat with venetoclax combination therapy. Patients provided written informed consent; collected data includes demographics, medical history, cytogenetic and molecular testing, tumor lysis syndrome (TLS) risk, concomitant treatments, adverse events, transfusion history, and International Working Group (IWG) response. This ongoing study will enroll approximately 200 patients from 20 sites across Canada. Primary endpoint for the study is overall survival. Interim analysis data were analyzed descriptively for quantitative variables. Complete remission (CR) plus complete remission with incomplete hematologic recovery (CRi) as per modified IWG criteria and incidence of treatment-emergent adverse events (TEAEs) were evaluated. Results: Sixty patients were included in this interim analysis, 59 dosed with venetoclax + AZA and 1 dosed with venetoclax + LDAC. The interim analysis included patients who had completed Cycle 3 through March 2024; expanded data is forthcoming as the study progresses. Patient ages ranged from 59 to 87 years, with a mean (SD) age of 74.6 (6.2). Over half (55.0%) of patients were over 75 years, and 23.3% were over 80 years. The majority of patients (68.3%) were male. 35.0% of patients had an ECOG-PS score of 0 or 1 and 20.0% had a score of ≥2 at baseline; for 45.0% of patients, baseline ECOG-PS score was not available. Distribution of patients by region was 40.0% in the West, 26.7% in Ontario, 13.3% in Québec, and 20.0% in the Atlantic. In the venetoclax + AZA cohort, 13 (22.0%) of patients received fluconazole, 5 (8.5%) received posaconazole, and 2 (3.4%) received voriconazole as prophylactic therapy. Overall, 36/51 (70.6%) patients had response assessments during Cycles 1, 2, and/or 3; of these evaluable patients, CR/CRi was achieved by 19/36 (52.8%) receiving venetoclax + AZA. In Cycle 1 CR/CRi was achieved by 12/28 patients (42.9%), in Cycle 2 by 10/19 patients (52.6%) and in Cycle 3 by 10/16 (62.5%) patients. The 1 patient who received venetoclax + LDAC did not have an assessment for CR/CRi. Bone marrow assessments were available for 47/59 (79.7%) of patients across Cycles 1 to 3; 34/59 (57.6%) in Cycle 1, 15/49 (30.6%) in Cycle 2, and 10/47 (21.3%) of patients in Cycle 3. Overall, 9 patients (15.3%) received granulocyte colony stimulating factors during Cycles 1, 2, and 3. Transfusion independence was reported for 52.0% of patients. Incidence of any TEAE occurred in 71.2% of patients receiving venetoclax + AZA. Serious TEAEs occurred in 42.4% of patients, febrile neutropenia was the most common serious TEAE (10.2%). Hematological TEAEs were more common than non-hematological events, 61.0% versus 40.7%; the most common hematological events were neutrophil count and platelet count decreased (27.1% each) and the most common non-hematological event was hypokalemia (6.8%). In Cycle 1, 3 patients receiving venetoclax + AZA met criteria for laboratory TLS per Howard criteria and 0 patients met criteria for clinical TLS. These patients did not discontinue venetoclax +AZA . Within the venetoclax + AZA cohort, in Cycles 1, 2, and 3, most patients (86.4%) had a venetoclax dosing duration of >21 days per 28-day cycle (overall range of 7 to 125 days). In Cycle 1, the mean duration of venetoclax treatment was 23.5 days with a mean daily dose of 254.2 mg. In Cycle 2, the mean duration of venetoclax treatment was 19.8 days with a mean daily dose of 302.4 mg. In Cycle 3, mean duration of venetoclax treatment was 18.6 days with a mean daily dose of 293.6 mg. Conclusion: This interim analysis reports data on the first 60 patients treated in Canadian practices with venetoclax from the prospective real-world LIVEN study. The safety profile is consistent with prior studies of venetoclax combination therapies, and cytopenia/neutropenia was managed by dose modifications.

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)0.008
metaresearch head score (Gemma)0.012
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 score0.210
Threshold uncertainty score0.423

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0080.012
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.002
Bibliometrics0.0010.003
Science and technology studies0.0020.001
Scholarly communication0.0010.000
Open science0.0020.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0030.000

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 head0.036
GPT teacher head0.359
Teacher spread0.322 · 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
Published2024
Admission routes2
Has abstractyes

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