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Record W4250479092 · doi:10.1093/jcag/gwy008.184

A183 SOFOSBUVIR-BASED ALL-ORAL REGIMENS FOR PATIENTS WITH CHRONIC HEPATITIS C GENOTYPE 3 INFECTION: INTEGRATED ANALYSIS OF FIVE CLINICAL STUDIES

2018· article· en· W4250479092 on OpenAlexaffabout
Graham R. Foster, Stefan Zeuzem, Edward Gane, Catherine Stedman, Jordan J. Feld, Alessandra Mangia, Kosh Agarwal, Mark G. Swain, H.M. Mir, Phil Troke, Joe Llewellyn, M. Natha, Bruce Kreter, J Zhang, J. McNally, Diana M. Brainard, Simone I. Strasser, Stephen Pianko

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2018
Typearticle
Languageen
FieldMedicine
TopicHepatitis C virus research
Canadian institutionsUniversity of CalgaryUniversity of TorontoUniversity Health Network
Fundersnot available
KeywordsSofosbuvirMedicineGenotypeChronic hepatitisInternal medicineHepatitis CVirologyGastroenterologyRibavirinBiologyVirusGenetics

Abstract

fetched live from OpenAlex

Hepatitis C virus (HCV) genotype 3 (GT3) infection represents the second most common genotype worldwide and is currently considered the most difficult genotype to treat. AASLD and EASL guidelines recommend sofosbuvir (SOF) based regimens for the treatment of patients with HCV GT3. This analysis evaluated the efficacy and safety of various 12-week SOF-based all-oral regimens for HCV GT3 from Phase 2 and 3 clinical studies In the phase 2 ELECTRON-2 study, 26 treatment-naïve (TN) and 50 treatment-experienced (TE) HCV GT3 patients received 12 weeks of ledipasvir 90 mg (LDV)/SOF 400 mg daily + weight-based ribavirin (RBV) 1000 or 1200 mg divided twice daily. In the phase 2 CANADA study, 111 TN HCV GT3 patients received 12 weeks of LDV/SOF+RBV. In the phase 3 ALLY-3 study, 101 TN and 51 TE HCV GT3 patients received 12 weeks of SOF 400mg + daclatasvir 60 mg (DCV) daily. In the phase 3 ALLY-3+ study, 6 TN and 18 TE HCV GT3 patients received 12 weeks of SOF+DCV+RBV. In the phase 3 ASTRAL-3 study, 206 TN and 71 TE HCV GT3 patients received 12 weeks of SOF 400 mg/velpatasvir 100 mg (VEL) daily, compared to 275 patients who received 24 weeks of SOF+RBV. Patients with compensated cirrhosis were allowed to enroll in all studies. 640 patients with HCV GT3 were enrolled in 5 clinical studies in North America, Europe, Australia, and New Zealand. Overall in all studies, the patients were male (62%), white (86%), and had IL28B non-CC genotype (61%). 190 patients (30%) were TE and 197 patients (31%) had compensated cirrhosis. Treatment responses will be reported. Therapy was well-tolerated with no patients discontinuing all treatment due to an adverse event. SOF/VEL for 12 weeks achieved the highest SVR12 and lowest relapse rates seen among the 5 studies, including in compensated cirrhotic patients, and was superior to 24 weeks of SOF+RBV. It offers a fixed-duration, IFN- and RBV-free, well-tolerated, and highly effective therapy, even for difficult-to-treat GT3 patients. Gilead Sciences Inc.

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)0.009
metaresearch head score (Gemma)0.004
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.009
Threshold uncertainty score0.047

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0090.004
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.003
Bibliometrics0.0020.002
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.035
GPT teacher head0.351
Teacher spread0.316 · 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 designMeta-analysis
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
Published2018
Admission routes2
Has abstractyes

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