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Record W7093123291

B03 | PELABRESIB IN COMBINATION WITH RUXOLITINIB FOR JANUS KINASE INHIBITOR-NAIVE PATIENTS WITH MYELOFIBROSIS: 72-WEEK FOLLOW-UP WITH LONG-TERM EFFICACY OUTCOMES OF THE PHASE III MANIFEST-2

2025· article· en· W7093123291 on OpenAlexaff

Bibliographic record

VenueDOAJ (DOAJ: Directory of Open Access Journals) · 2025
Typearticle
Languageen
FieldMedicine
TopicMyeloproliferative Neoplasms: Diagnosis and Treatment
Canadian institutionsPrincess Margaret Cancer Centre
Fundersnot available
KeywordsRuxolitinibMyelofibrosisAnemiaAdverse effectPlaceboBone marrowRandomizationHemoglobinPhases of clinical research
DOInot available

Abstract

fetched live from OpenAlex

Background. Pelabresib (PELA) is an investigational, oral, small molecule inhibiting BET proteins and BET-mediated expression of genes involved in Myelofibrosis (MF) pathogenesis. The Phase III MANIFEST-2 study (NCT04603495) evaluates the efficacy and safety of PELA plus ruxolitinib (RUX) in MF patients (pts). We report Week 72 results, including PFS, OS and Leukemia Free Survival (LFS). Methods. Pts with a DIPSS ≥ Intermediate-1 risk, platelet ≥100 ×109/L, spleen volume ≥450 cm3, ≥2 symptoms with average score ≥3 or total symptom score (TSS) ≥10 (MF SAF v4.0), peripheral blasts <5%, and ECOG performance status ≤2 were randomized 1:1 to PELA+RUX or placebo (PBO)+RUX. Week 72 assessments included spleen volume reduction (SVR35) ≥35% from baseline (bsl), absolute TSS change, TSS50 (≥50% TSS reduction from bsl), hemoglobin (Hb) response (≥1.5 g/dL mean Hb increase from bsl without transfusion in prior 12 weeks), bone marrow fibrosis (BMF) grade improvement, and safety. PFS (time from randomization to progression, or death from any cause), OS, and LFS were analysed (study not powered for survival outcomes). Results. As of August 30, 2024, 67.8% (145/214) of pts in PELA+RUX arm and 72.7% (157/216) in PBO+RUX remained on study (median follow-up 92 weeks). SVR35, absolute TSS change, and ≥1 grade BMF improvement favored PELA+RUX (Table I). In pts with bsl Hb <10 g/dL, Hb response was observed in 20.9% (14/67; 95% CI: 11.16–30.63) vs 16.9% (12/71; 95% CI: 8.18–25.62) for PELA+RUX vs PBO+RUX. Of 426 pts, Grade ≥3 treatment-emergent adverse events (TEAEs) occurred in 65.1% vs 65.4%, Grade ≥3 anemia in 27.4% vs 41.1%, thrombocytopenia in 17.0% vs 7.0% for PELA+RUX vs PBO+RUX. Accelerated and blast-phase progression, adjudicated independently by external experts, was reported in 6.1% (13/214) vs 4.2% (9/214), respectively. Comparing PELA+RUX vs PBO+RUX, the PFS hazard ratio (HR) was 0.874 (95% CI: 0.49–1.56), OS HR 0.932 (95% CI: 0.53–1.66), and LFS HR 0.994 (95% CI: 0.57–1.72). Conclusion. At 72 weeks, PELA+RUX showed sustained improvements in splenic response, symptoms, SVR35/TSS50 dual response, BMF, and anemia vs PBO+RUX. Grade ≥3 TEAEs were similar and consistent between arms, with decreased imbalance in leukemic transformation over time and favorable trend in survival for PELA+RUX. Overall results suggest that PELA+RUX provides meaningful clinical benefits over RUX alone and support evidence of ongoing disease modification.

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)0.001
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: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.013

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0040.001

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 head0.094
GPT teacher head0.472
Teacher spread0.379 · 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 designRandomized 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".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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