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Record W4384943566 · doi:10.1097/txd.0000000000001505

Cancer Risk Following HLA-Incompatible Living Donor Kidney Transplantation

2023· article· en· W4384943566 on OpenAlexfundno aff
Jennifer D. Motter, Allan B. Massie, Jacqueline Garonzik‐Wang, Ruth M. Pfeiffer, Kelly J. Yu, Dorry L. Segev, Eric A. Engels

Bibliographic record

VenueTransplantation Direct · 2023
Typearticle
Languageen
FieldMedicine
TopicViral-associated cancers and disorders
Canadian institutionsnot available
FundersSchool of Medicine, University of North Carolina at Chapel HillU.S. National Library of MedicineNational Institute of Environmental Health SciencesNational Institute of Diabetes and Digestive and Kidney DiseasesNational Institute of Allergy and Infectious DiseasesNational Cancer InstituteNational Center for Chronic Disease Prevention and Health PromotionNational Heart, Lung, and Blood InstituteUniversity of California, San DiegoSchool of Medicine, Emory UniversityThomas Jefferson UniversityUniversity of Illinois at Urbana-ChampaignHealth Resources and Services AdministrationYork UniversityMassachusetts General HospitalHouston Methodist HospitalUniversity of California, San FranciscoVanderbilt University Medical CenterVanderbilt UniversityVirginia Commonwealth UniversityUniversity of Wisconsin-MadisonUniversity of Illinois at ChicagoCedars-Sinai Medical CenterHouston Methodist Research InstituteNYU Langone Medical CenterEmory UniversityCleveland ClinicWeill Cornell Medical CollegeUniversity of PennsylvaniaNational Institutes of HealthU.S. Department of Health and Human Services
KeywordsMedicineHazard ratioCancer registryInternal medicineCancerColorectal cancerIncidence (geometry)Proportional hazards modelOncologyImmunosuppressionKidney transplantationCohortTransplantationKidney cancerConfidence interval

Abstract

fetched live from OpenAlex

Incompatible living donor kidney transplant recipients (ILDKTr) require desensitization to facilitate transplantation, and this substantial upfront immunosuppression may result in serious complications, including cancer. Methods: To characterize cancer risk in ILDKTr, we evaluated 858 ILDKTr and 12 239 compatible living donor kidney transplant recipients (CLDKTr) from a multicenter cohort with linkage to the US transplant registry and 33 cancer registries (1997-2016). Cancer incidence was compared using weighted Cox regression. Results: Among ILDKTr, the median follow-up time was 6.7 y (maximum 16.1 y) for invasive cancers (ascertained via cancer registry linkage) and 5.0 y (maximum 16.1 y) for basal and squamous cell carcinomas (ascertained via the transplant registry and censored for transplant center loss to follow-up). Invasive cancers occurred in 53 ILDKTr (6.2%) and 811 CLDKTr (6.6%; weighted hazard ratio [wHR] 1.01; 95% confidence interval [CI], 0.76-1.35). Basal and squamous cell carcinomas occurred in 41 ILDKTr (4.8%) and 737 CLDKTr (6.0%) (wHR 0.99; 95% CI, 0.69-1.40). Cancer risk did not vary according to donor-specific antibody strength, and in an exploratory analysis, was similar between CLDKTr and ILDKTr for most cancer types and according to cancer stage, except ILDKTr had a suggestively increased risk of colorectal cancer (wHR 3.27; 95% CI, 1.23-8.71); however, this elevation was not significant after correction for multiple comparisons. Conclusions: These findings indicate that the risk of cancer is not increased for ILDKTr compared with CLDKTr. The possible elevation in colorectal cancer risk is unexplained and might suggest a need for tailored screening or prevention.

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)0.000
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 score0.036
Threshold uncertainty score0.845

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
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 head0.015
GPT teacher head0.284
Teacher spread0.269 · 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

Citations4
Published2023
Admission routes1
Has abstractyes

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