MétaCan
Menu
Back to cohort
Record W2912512558 · doi:10.1111/ijd.14391

Influence of the phenotype on mycosis fungoides prognosis, a retrospective cohort study of 160 patients

2019· article· en· W2912512558 on OpenAlexafffundabout
Alejandra Jaque, Alexandra Mereniuk, Scott R. Walsh, Neil H. Shear, Brandon Zagorski, Raed Alhusayen

Bibliographic record

VenueInternational Journal of Dermatology · 2019
Typearticle
Languageen
FieldMedicine
TopicCutaneous lymphoproliferative disorders research
Canadian institutionsUniversity of TorontoHealth Sciences CentreInstitute for Work & HealthSunnybrook Health Science Centre
FundersCanadian Dermatology Foundation
KeywordsMycosis fungoidesMedicineCD8Retrospective cohort studyCD4-CD8 RatioCohortDemographicsImmunophenotypingInternal medicineStage (stratigraphy)ConfoundingGastroenterologyImmunologyDemographyLymphomaLymphocyte subsetsFlow cytometryImmune systemBiology

Abstract

fetched live from OpenAlex

Abstract Background Mycosis fungoides ( MF ) typically has a CD 4 + CD 8 − T‐cell phenotype. Rare cases of CD 4 − CD 8 + , CD 4 − CD 8 − , or CD 4 + CD 8 + immunophenotypes have been described. Little is known about the impact of MF immunophenotypes on disease behavior. Methods We conducted a retrospective cohort study to review all cases of MF from 2007 to 2017 from Sunnybrook Health Sciences Centre, Toronto, Canada. CD 4 + CD 8 − (Group 1) was compared to the three less common subtypes (Group 2) with respect to stage at diagnosis, progression, and transformation. Potential confounding factors (demographic, clinical, and laboratory parameters) were assessed. Results A total of 160 patients with confirmed MF were analyzed, including 126 CD 4 + CD 8 − MF (79%), 26 CD 4 − CD 8 + MF (16%), six CD 4 + CD 8 + MF (4%), and two CD 4 − CD 8 − MF (1%). Both groups were similar with respect to demographics and laboratory parameters at the time of diagnosis. There was no difference between patients with late stage disease (10% vs. 9%) for groups 1 and 2, respectively ( P = 0.901). There was no statistically significant difference either in 5‐year progression (27.7% vs. 23.5%, P = 0.283) or transformation (16.2% vs. 17.3%, P = 0.350) estimates. We did find that atypical immunophenotypes presented with different clinical morphologies and were less likely to require systemic therapy. Conclusion Our large cohort study indicates that atypical MF immunophenotypes do not seem to influence prognosis. Hypopigmented MF was more frequent in the CD 4 − CD 8 + group while folliculotropic MF was exclusively seen in the CD 4 + CD 8 − group. We believe that cases of CD 8 + MF with aggressive behavior described in the literature represent misclassified primary cutaneous aggressive epidermotropic CD 8 + T‐cell lymphoma. The small number of patients included in the study is a limiting factor.

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)0.000
metaresearch head score (Gemma)0.001
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 score0.006
Threshold uncertainty score0.258

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
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 head0.008
GPT teacher head0.296
Teacher spread0.288 · 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".

Quick stats

Citations11
Published2019
Admission routes3
Has abstractyes

Explore more

Same venueInternational Journal of DermatologySame topicCutaneous lymphoproliferative disorders researchFrench-language works237,207