Evidence map›Paper›PMID 38825628›Full record

ArticleAnnals of surgical oncology2024

Validation of the AJCC 8th Edition Breast Cancer Prognostic Staging System in Legacy Alliance Trials (AFT-01).

Laura K Krecko, Heather B Neuman, Caprice C Greenberg, Lee G Wilke, Bret M Hanlon, Stephen B Edge, Kathryn J Ruddy, Ann H Partridge, Jennifer Le-Rademacher, Dou-Yan Yang and 2 more

Registry-linked trialAbstract readValidation Study
In one paragraph

Article in Annals of surgical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02171078 (Post-Treatment Surveillance in Breast Cancer), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02171078 completednot on this map

Post-Treatment Surveillance in Breast Cancer: Bringing Cost Effectiveness Research (CER) to the Alliance

TypeobservationalSponsorUniversity of Wisconsin, MadisonRan2014 to 2017Enrolled34,359ConditionsBreast Neoplasms
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Laura K KreckoDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Heather B NeumanDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Caprice C GreenbergDepartment of Surgery, University of North Carolina-Chapel Hill, Chapel Hill, NC, USA.
Lee G WilkeDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Bret M HanlonDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Stephen B EdgeDepartment of Surgical Oncology, Roswell Park Comprehensive Cancer Center and University at Buffalo, Buffalo, NY, USA.
Kathryn J RuddyDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Ann H PartridgeDepartment of Medical Oncology, Dana Farber/Partners CancerCare, Boston, MA, USA.
Jennifer Le-RademacherDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Dou-Yan YangDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Jeffrey HavlenaDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Jessica R SchumacherDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA. jessica_schumacher@med.unc.edu.

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
UW Surgical Oncology Research Training Program (UW-SORT)T32CA090217 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Muhammed Murtaza, Heather B Neuman · 2001 to 2026
$8.3M
BUILDING INTERDISCIPLINARY RESEARCH CAREER IN WOMEN'S HEALTH (BIRCWH) SCHOLARSK12HD055894 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI BURNSIDE, ELIZABETH S · 2007 to 2016
$4.1M
Eunice Kennedy Shriver National Institute of Child Health and Human Development K12HD055894NCI NIH HHS T32 CA090217NCI NIH HHS T32CA090217NCI NIH HHS U10 CA180821NCI NIH HHS U10CA180821NCI NIH HHS UG1 CA233180NICHD NIH HHS K12 HD055894Patient-Centered Outcomes Research Institute CE-1304-6543
6 · The paper itself

Abstract

backgroundThe 8th edition American Joint Committee on Cancer staging system combined anatomic stage (AS) with receptor status and grade to create prognostic stage (PS). PS has been validated in single-institution and cancer registry studies; however, missing human epidermal growth factor receptor 2 (HER2) status and variable treatment and follow-up create limitations.

objectiveOur objective was to compare the relative prognostic ability of PS versus AS to predict survival using breast cancer clinical trial data.

methodsWomen with non-metastatic breast cancer enrolled in six Alliance for Clinical Trials in Oncology trials were included (enrollment years 1997-2010). AS and PS were constructed using pathological tumor size, nodal status, estrogen receptor (ER), progesterone receptor (PR), HER2 status, and grade. Unadjusted Cox proportional hazard models were estimated to predict overall survival within 5 years, with AS and PS as predictor variables. The relative predictive power of staging models was assessed by comparing Harrell concordance indices (C-indices). Kaplan-Meier-based mortality estimates were compared by stage.

resultsOverall, 6924 women were included (median age 53 years); 45.2% were diagnosed with ER+/PR+/HER2- tumors, 26.2% with HER2+ tumors, and 17.1% with ER-/PR-/HER2- tumors. Median follow-up time was 5 years (interquartile range 2.95-5.00). PS significantly improved predictive performance (C-index 0.721) for overall survival compared with AS (0.700) (p = 0.020). Kaplan-Meier hazard estimates suggested PS did not distinguish mortality risk between patients with IIB and IIIA or IB and IIA disease.

conclusionsPS has significantly improved predictive performance for OS compared with AS. As systemic therapies evolve, it will be important to re-evaluate the prognostic staging system, particularly for patients with intermediate-stage cancers. CLINICALTRIALS: gov Identifier: NCT02171078.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesNeoplasm StagingReceptors, EstrogenReceptors, ProgesteroneAdultAgedClinical Trials as TopicFemaleFollow-Up StudiesHumansMiddle AgedNeoplasm GradingPrognosisSurvival RateERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneAmerican Joint Committee on CancerAnatomic stageBreast cancerClinical trialPrognostic stage

Identifiers

PMID38825628
PMCPMC11460990

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.