MétaCan
Menu
Back to cohort
Record W2725102643 · doi:10.1093/jnci/92.9.757

Re: Weighing the Risks and Benefits of Tamoxifen Treatment for Preventing Breast Cancer

2000· letter· en· W2725102643 on OpenAlexaff
Judy Norsigian

Bibliographic record

VenueJNCI Journal of the National Cancer Institute · 2000
Typeletter
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsCancerCare Manitoba
Fundersnot available
KeywordsTamoxifenBreast cancerMedicineCancerFamily medicineClinical trialGynecologyOncologyInternal medicine

Abstract

fetched live from OpenAlex

In April 1998, the Breast Cancer Prevention Trial (P-1) was halted 14 months early because of a 45% reduction in breast cancer among those patients receiving tamoxifen. At that time, all of the major networks and newspapers made a lead story out of the National Cancer Institute's announcement of this finding. Many of the media reports repeated the investigators' contention that the trial's entry criteria identified women who are potentially eligible for tamoxifen therapy, e.g., all women over the age of 60 years (1). Now, 1½ years later, the Journal has published a special article entitled “Weighing the Risks and Benefits of Tamoxifen Treatment for Preventing Breast Cancer” (2). Its authors assessed the data from the Breast Cancer Prevention Trial P-1 (3) and estimate that the benefits of taking tamoxifen substantially outweigh the risks only for younger high-risk women; conversely, the risks might outweigh the benefits for most black women older than 60 years of age and most white women older than 60 years with a uterus. In other words, tamoxifen therapy is an appropriate consideration for a much smaller subset of high-risk women than was originally thought. The Journal special article (2) states that the risk/benefit assessment grew out of a National Cancer Institute-sponsored workshop held in July 1998. Why did it take so long to get this assessment into print? By contrast, results of the P-1 trial were published by the Journal less than 6 months after the trial ended. Until this assessment was published, it was not known which women are at enough of a high risk to make tamoxifen's potentially fatal side effects worth its potential benefits. Yet as early as October 1998, tamoxifen received U.S. Food and Drug Administration (FDA) approval for risk reduction which, in turn, allowed its producer, AstraZeneca (Wilmington, DE), to mount an immediate and extensive direct-to-consumer advertising campaign. At the time, we believed that the FDA approval was premature; this assessment only confirms our conviction. For the first time, an anticancer drug is being marketed to healthy people; more care should have been taken beforehand to estimate who can safely benefit from tamoxifen.

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)0.014
metaresearch head score (Gemma)0.112
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Commentary · Consensus signal: Commentary
Teacher disagreement score0.051
Threshold uncertainty score0.170

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0140.112
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0030.001
Science and technology studies0.0010.002
Scholarly communication0.0060.006
Open science0.0020.002
Research integrity0.0060.009
Insufficient payload (model declined to judge)0.0510.029

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 head0.073
GPT teacher head0.350
Teacher spread0.277 · 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 designNot applicable
Domainnot available
GenreCommentary

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

Citations4
Published2000
Admission routes1
Has abstractyes

Explore more

Same venueJNCI Journal of the National Cancer InstituteSame topicBRCA gene mutations in cancerFrench-language works237,207