Evidence map›Paper›PMID 36872873›Full record

ArticleCancer2023

The influence of anatomic stage and receptor status on first recurrence for breast cancer within 5 years (AFT-01).

Heather B Neuman, Jessica R Schumacher, Stephen B Edge, Kathryn J Ruddy, Ann H Partridge, Menggang Yu, David J Vanness, Bret M Hanlon, Jennifer G Le-Rademacher, Dou-Yan Yang and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in Cancer, 2023. 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

13 authors.

Heather B NeumanDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.ORCID 0000-0001-7462-8333
Jessica R SchumacherDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.ORCID 0000-0002-6740-9498
Stephen B EdgeDepartments of Surgical Oncology and Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Kathryn J RuddyDepartment of Oncology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-6298-332X
Ann H PartridgeDepartment of Medical Oncology, Dana-Farber/Partners Cancer Care, Boston, Massachusetts, USA.ORCID 0000-0002-4722-4824
Menggang YuDepartment of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin, USA.
David J VannessDepartment of Health Policy and Administration, Penn State College of Health and Human Development, Hershey, Pennsylvania, USA.
Bret M HanlonDepartment of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin, USA.ORCID 0000-0002-4517-1204
Jennifer G Le-RademacherAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-2234-7430
Dou-Yan YangDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Jeffrey HavlenaDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Carrie A StrandAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota, USA.
Caprice C GreenbergDepartment of Surgery, Medical College of Georgia at Augusta University, Augusta, Georgia, USA.

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
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
BUILDING INTERDISCIPLINARY RESEARCH CAREER IN WOMEN'S HEALTH (BIRCWH) SCHOLARSK12HD055894 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI BURNSIDE, ELIZABETH S · 2007 to 2016
$4.1M
NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180882NCI NIH HHS UG1 CA233180NICHD NIH HHS K12 HD055894
6 · The paper itself

Abstract

backgroundRisk-stratified follow-up guidelines that account for the absolute risk and timing of recurrence may improve the quality and efficiency of breast cancer follow-up. The objective of this study was to assess the relationship of anatomic stage and receptor status with timing of the first recurrence for patients with local-regional breast cancer and generate risk-stratified follow-up recommendations.

methodsThe authors conducted a secondary analysis of 8007 patients with stage I-III breast cancer who enrolled in nine Alliance legacy clinical trials from 1997 to 2013 (ClinicalTrials.gov identifier NCT02171078). Patients who received standard-of-care therapy were included. Patients who were missing stage or receptor status were excluded. The primary outcome was days from the earliest treatment start date to the date of first recurrence. The primary explanatory variable was anatomic stage. The analysis was stratified by receptor type. Cox proportional-hazards regression models produced cumulative probabilities of recurrence. A dynamic programming algorithm approach was used to optimize the timing of follow-up intervals based on the timing of recurrence events.

resultsThe time to first recurrence varied significantly between receptor types (p < .0001). Within each receptor type, stage influenced the time to recurrence (p < .0001). The risk of recurrence was highest and occurred earliest for estrogen receptor (ER)-negative/progesterone receptor (PR)-negative/Her2neu-negative tumors (stage III; 5-year probability of recurrence, 45.5%). The risk of recurrence was lower for ER-positive/PR-positive/Her2neu-positive tumors (stage III; 5-year probability of recurrence, 15.3%), with recurrences distributed over time. Model-generated follow-up recommendations by stage and receptor type were created.

conclusionsThis study supports considering both anatomic stage and receptor status in follow-up recommendations. The implementation of risk-stratified guidelines based on these data has the potential to improve the quality and efficiency of follow-up.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleHumansNeoplasm Recurrence, LocalReceptors, EstrogenReceptors, ProgesteroneErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, Progesteronebreast cancerfollow-upreceptorrecurrencestage

Identifiers

PMID36872873
PMCPMC10424512

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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.