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Record W2622897264 · doi:10.1002/hon.2437_57

DYNAMO: a PHASE 2 STUDY DEMONSTRATING THE CLINICAL ACTIVITY OF DUVELISIB IN PATIENTS WITH DOUBLE‐REFRACTORY INDOLENT NON‐HODGKIN LYMPHOMA

2017· article· en· W2622897264 on OpenAlexaff
Pier Luigi Zinzani, Nina D. Wagner‐Johnston, Carole B. Miller, Kirit M. Ardeshna, S. Tertreault, Sarit Assouline, Jiřı́ Mayer, Francesco Passamonti, Scott D. Lunin, Andrew R. Pettitt, Zsolt Nagy, Olivier Tournilhac, Karim Abou-Nassar, Michael Crump, E. Jacobsen, Sven de Vos, Hagop Youssoufian, Jane Porter, Ian W. Flinn

Bibliographic record

VenueHematological Oncology · 2017
Typearticle
Languageen
FieldMedicine
TopicChronic Lymphocytic Leukemia Research
Canadian institutionsPrincess Margaret Cancer CentreCégep de l'OutaouaisJewish General Hospital
Fundersnot available
KeywordsMedicineInternal medicineAdverse effectRefractory (planetary science)GastroenterologyClinical endpointRegimenLymphomaSurgeryOncologyClinical trial

Abstract

fetched live from OpenAlex

Introduction: Duvelisib is an oral, dual inhibitor of PI3K-δ,γ being developed to treat hematologic malignancies. Methods: DYNAMO is an open-label, single-arm, safety, and efficacy study in patients (pts) with follicular lymphoma (FL), small lymphocytic lymphoma (SLL), or marginal zone lymphoma (MZL), whose disease is double-refractory to rituximab and to chemotherapy or radioimmunotherapy. Pts received duvelisib 25 mg BID in 28-day cycles until disease progression or unacceptable toxicity. The primary endpoint is overall response rate (ORR) as assessed by an independent review committee (IRC) per revised IWG criteria, with significance tested against the null hypothesis that ORR was ≤30% per IRC. Secondary endpoints include duration of response (DoR), progression-free survival (PFS), overall survival (OS), time to response (TTR), adverse events (AEs), and changes in safety laboratory values. Pneumocystis jiroveci pneumonia (PJP) prophylaxis was mandated for all pts. Results: 129 pts received duvelisib (FL = 83; SLL = 28; MZL = 18) with a median duration of exposure of 6 mo. (range 0.4 - 24). Median age was 65 years; 68% were male. Median time from last anticancer therapy to first dose of duvelisib was 3.5 months. Pts received a median of 3 prior anticancer regimens (range 1 - 18), and 40% of pts ≥ 4 regimens. 77% had disease refractory to ≥2 anticancer regimens and 96% were refractory to their last anticancer regimen. IRC-assessed ORR was 46% (p = 0.0001) (all PRs), and Investigator-assessed ORR was 58% (2 CRs). Median TTR was 1.9 mo. (range 1.4 – 11.7). 83% of pts had reduction in nodal target lesions after treatment with duvelisib. AEs were mostly Gr 1-2. Most common ≥ Gr 3 AEs were transient cytopenias (neutropenia [23%], anemia [12%], and thrombocytopenia [10%]), and diarrhoea (15%). 17% of pts discontinued duvelisib due to an AE. Opportunistic infections occurred in <5% of pts, none fatal, and were: 1 pt with pneumocystis; 3 pts with CMV infections. Six pts had an AE with outcome of death. Conclusions: In DYNAMO, duvelisib met its primary efficacy endpoint for ORR (p-value = 0.0001 against null hypothesis that ORR ≤ 30%) in a double-refractory iNHL population, with a 46% ORR, med. DoR 9.9 mo., and 83% with reduction in target lesions. Duvelisib was generally well tolerated, with a manageable safety profile with appropriate risk mitigation. Duvelisib monotherapy has a favorable benefit-risk profile in double-refractory iNHL, and may represent an important treatment option. Mature clinical data will be available at the time of presentation. Keywords: indolent lymphoma; PI3K/AKT/mTOR; small lymphocytic lymphoma (SLL). NE = not estimable * Median follow-up 11.5 mo.

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)0.002
metaresearch head score (Gemma)0.002
Version: codex-gemma-dda1882f352aValidation 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 score0.148
Threshold uncertainty score0.830

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0010.000
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 head0.086
GPT teacher head0.452
Teacher spread0.367 · 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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Citations16
Published2017
Admission routes1
Has abstractyes

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