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Record W2898319351 · doi:10.1093/annonc/mdy297.008

Magnitude of clinical benefit of trials supporting US Food and Drug Administration (FDA) approval of breakthrough and non-breakthrough drugs

2018· article· en· W2898319351 on OpenAlexaff
C. Moltó Valiente, María Borrell, Thomas J. Hwang, Ignasi Gich Saladich, Agustí Barnadas, Eitan Amir, Aaron S. Kesselheim, Ariadna Tibau

Bibliographic record

VenueAnnals of Oncology · 2018
Typearticle
Languageen
FieldEconomics, Econometrics and Finance
TopicHealth Systems, Economic Evaluations, Quality of Life
Canadian institutionsPrincess Margaret Cancer CentreUniversity of Toronto
Fundersnot available
KeywordsMedicineClinical trialFood and drug administrationDrugClinical researchRandomized controlled trialSample size determinationIntensive care medicineInternal medicinePharmacologyOncology

Abstract

fetched live from OpenAlex

Background: The Breakthrough Therapy program was established in July 2012 to expedite drug development and approval in the US, although it is unclear if cancer drugs qualifying for this program are more effective or safer than non-breakthrough-designated drugs. The European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS) is a validated tool to assess the clinical benefit of cancer drugs. Here, we compare the magnitude of clinical benefit of clinical trials leading to FDA approval of breakthrough-designated and non-breakthrough-designated cancer drugs. Methods: We searched the [email protected] website to identify anticancer drugs for solid tumors approved by the FDA between July 2012 and December 2017. For each drug, we collected data on breakthrough therapy designation, pivotal trial design, efficacy, safety, and quality of life outcomes, and applied ESMO-MCBS v1.1 grades. Substantial benefit was defined as a grade of A or B for trials of curative intent and 4 or 5 for those of palliative intent. Trial characteristics and ESMO-MCBS grades were compared using Chi squared or Mann Whitney U tests. Results: We identified 110 trials supporting the approval of 52 individual drugs for 96 indications. Of these indications, 49% received breakthrough designation. Compared to non-breakthrough drugs, trials supporting breakthrough drugs had a smaller sample size (median 401 vs 604, P=.047), were less likely to evaluate experimental cytotoxic chemotherapy or endocrine therapy than targeted therapy (0% vs 10%, P=.004), and were less often randomized (60% vs 84%; P=.009) or double-blind (15% vs 46%, P=.001). A similar proportion of trials supporting breakthrough and non-breakthrough drugs approved for palliative intent showed substantial clinical benefit using ESMO-MCBS v1.1 (36% vs 29%; P=.45). There were too few trials performed with curative intent (n = 10) to perform statistical testing. Conclusions: Compared to non-breakthrough drugs, trials of breakthrough drugs are smaller and more likely to be single-arm and not double-blinded. A similarly low proportion of breakthrough and non-breakthrough cancer drugs met the standard of substantial clinical benefit as applied in ESMO-MCBS v1.1. Legal entity responsible for the study: Hospital de la Santa Creu i Sant Pau. Funding: Has not received any funding. Disclosure: All authors have declared no conflicts of interest.

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)0.154
metaresearch head score (Gemma)0.308
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesMetaresearch, Meta-epidemiology (broad)
Consensus categoriesnone
DomainCandidate signal: Evaluation · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.998
Threshold uncertainty score0.814

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.1540.308
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.004
Bibliometrics0.0050.006
Science and technology studies0.0010.002
Scholarly communication0.0040.003
Open science0.0010.003
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0050.000

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 head0.603
GPT teacher head0.575
Teacher spread0.028 · 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.

Study designMeta-analysis
DomainEvaluation
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 routes1
Has abstractyes

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