Evidence map›Paper›PMID 37991939›Full record

Trial reportJNCI cancer spectrum2023

The prognostic and predictive effect of body mass index in hormone receptor-positive breast cancer.

Senna W M Lammers, Sandra M E Geurts, Irene E G van Hellemond, Astrid C P Swinkels, Carolien H Smorenburg, Maurice J C van der Sangen, Judith R Kroep, Hiltje de Graaf, Aafke H Honkoop, Frans L G Erdkamp and 6 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JNCI cancer spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00301457 (A Prospective Randomised, Open, Multicentre, Phase III Study to Assess Different Durations of Anastrozole Therapy After 2 to 3 Years Tamoxifen as Adjuvant Therapy in Postmenopausal Women With Breast Cancer.), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 12% of its field
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.

NCT00301457 phase3completednot on this map

A Prospective Randomised, Open, Multicentre, Phase III Study to Assess Different Durations of Anastrozole Therapy After 2 to 3 Years Tamoxifen as Adjuvant Therapy in Postmenopausal Women With Breast Cancer.

TypeinterventionalSponsorMaastricht University Medical CenterRan2006 to 2022Enrolled1,914ConditionsBreast CancerArmsAnastrozole
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

16 authors at 10 institutions in 1 country.

Senna W M LammersDepartment of Medical Oncology, Maastricht University Medical Centre, GROW, Maastricht University, Maastricht, the Netherlands.ORCID 0000-0002-8279-585X
Sandra M E GeurtsDepartment of Medical Oncology, Maastricht University Medical Centre, GROW, Maastricht University, Maastricht, the Netherlands.
Irene E G van HellemondDepartment of Medical Oncology, Catharina Hospital, Eindhoven, the Netherlands.
Astrid C P SwinkelsClinical research department, Netherlands Comprehensive Cancer Organisation (IKNL), Nijmegen, the Netherlands.
Carolien H SmorenburgDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Maurice J C van der SangenDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, the Netherlands.
Judith R KroepDepartment of Medical Oncology, Leiden University Medical Centre, Leiden, the Netherlands.
Hiltje de GraafDepartment of Medical Oncology, Medical Centre Leeuwarden, Leeuwarden, the Netherlands.
Aafke H HonkoopDepartment of Medical Oncology, Isala Clinics, Zwolle, the Netherlands.
Frans L G ErdkampDepartment of Medical Oncology, Zuyderland Medical Centre Heerlen-Sittard-Geleen, location Sittard-Geleen, the Netherlands.
Wilfred K de RoosDepartment of Surgery, Gelderse Vallei Hospital, Ede, the Netherlands.
Sabine C LinnDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0001-5541-0347
Alexander L T ImholzDepartment of Medical Oncology, Deventer Hospital, Deventer, the Netherlands.
Marjolein L SmidtDepartment of Surgery, Maastricht University Medical Centre, GROW, Maastricht University, Maastricht, the Netherlands.
Ingeborg J H VriensDepartment of Medical Oncology, Maastricht University Medical Centre, GROW, Maastricht University, Maastricht, the Netherlands.
Vivianne C G Tjan-HeijnenDepartment of Medical Oncology, Maastricht University Medical Centre, GROW, Maastricht University, Maastricht, the Netherlands.ORCID 0000-0002-3935-7440
Maastricht University Medical Centre · NLRadboud University Nijmegen · NLThe Netherlands Cancer Institute · NLDeventer Ziekenhuis · NLIsala · NLLeiden University Medical Center · NLMedisch Centrum Leeuwarden · NLNetherlands Comprehensive Cancer Organisation · NLZiekenhuis Gelderse Vallei · NLZuyderland Medisch Centrum · NL

Funding

AstraZeneca
6 · The paper itself

Abstract

backgroundObesity has been associated with an adverse prognosis and reduced efficacy of endocrine therapy in patients with hormone receptor-positive (HR+) breast cancer (BC). This study determines the prognostic and predictive effect of body mass index (BMI) on the disease-free survival (DFS) of postmenopausal HR+ BC patients.

methodsPatients were identified from the DATA study (NCT00301457), a randomized controlled trial evaluating the efficacy of 6 vs 3 years of anastrozole after 2 to 3 years of adjuvant tamoxifen in postmenopausal women with HR+ BC. Patients were classified as normal weight (BMI: 18.5-24.9 kg/m2), overweight (25.0-29.9 kg/m2), or obese (≥30.0 kg/m2). The primary endpoint was DFS, evaluated from randomization (prognostic analyses) or 3 years after randomization onwards (predictive analyses; aDFS) using multivariable Cox regression analyses. P-values were 2-sided.

resultsThis study included 678 normal weight, 712 overweight, and 391 obese patients. After a median follow-up of 13.1 years, overweight and obesity were identified as negative prognostic factors for DFS (hazard ratio (HR) = 1.16; 95% confidence interval (CI) = 0.97 to 1.38 and HR = 1.26; 95% CI = 1.03 to 1.54, respectively). The adverse prognostic effect of BMI was observed in women aged younger than 60 years, but not in women aged 60 years or older (P-interaction = .009). The effect of extended anastrozole on aDFS was similar in normal weight (HR = 1.00; 95% CI = 0.74 to 1.35), overweight (HR = 0.74; 95% CI = 0.56 to 0.98), and obese patients (HR = 0.97; 95% CI = 0.69 to 1.36) (P-interaction = .24).

conclusionIn this study among 1781 HR+ BC patients, overweight and obesity were adverse prognostic factors for DFS. BMI did not impact the efficacy of extended anastrozole.

Indexed as

Breast NeoplasmsAnastrozoleBody Mass IndexFemaleHumansObesityOverweightPrognosisAnastrozole

Identifiers

PMID37991939
PMCPMC10697786
OpenAlexW4388893308

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.