Evidence map›Paper›PMID 31292269›Full record

ArticleThe oncologist2019

Fracture Risk in Women with Breast Cancer Initiating Aromatase Inhibitor Therapy: A Registry-Based Cohort Study.

William D Leslie, Suzanne N Morin, Lisa M Lix, Saroj Niraula, Eugene V McCloskey, Helena Johansson, Nicholas C Harvey, John A Kanis

Abstract read
In one paragraph

Article in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Differential fracture risk in breast cancer patients based on endocrine therapy and age: a nationwide cohort study.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
    Article
  4. Review
  5. The impact of bone mineral density screening on incident fractures and healthcare resource utilization among postmenopausal breast cancer survivors treated with aromatase inhibitors.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2022
    Article
  6. Article
  7. Review
  8. Review
  9. 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

8 authors at 5 institutions in 3 countries.

William D LeslieUniversity of Manitoba, Winnipeg, Canada bleslie@sbgh.mb.ca.ORCID 0000-0002-1056-1691
Suzanne N MorinMcGill University, Montreal, Canada.
Lisa M LixUniversity of Manitoba, Winnipeg, Canada.
Saroj NiraulaUniversity of Manitoba, Winnipeg, Canada.
Eugene V McCloskeyCentre for Metabolic Bone Diseases, University of Sheffield Medical School, Sheffield, United Kingdom.
Helena JohanssonCentre for Metabolic Bone Diseases, University of Sheffield Medical School, Sheffield, United Kingdom.
Nicholas C HarveyMedical Research Council (MRC) Lifecourse Epidemiology Unit, University of Southampton, Southampton, United Kingdom.
John A KanisCentre for Metabolic Bone Diseases, University of Sheffield Medical School, Sheffield, United Kingdom.
University of Manitoba · CAUniversity of Sheffield · GBAustralian Catholic University · AUMcGill University · CANational Health Service · GB

Funding

Medical Research Council MC_U147585819Medical Research Council MC_U147585824Medical Research Council MC_U147585827Versus Arthritis 17702
6 · The paper itself

Abstract

backgroundAromatase inhibitors (AIs) used in breast cancer induce loss in bone mineral density (BMD) and are reported to increase fracture risk. MATERIALS AND

methodsUsing a population-based BMD registry, we identified women aged at least 40 years initiating AIs for breast cancer with at least 12 months of AI exposure (

resultsAt baseline, AI users had higher body mass index (BMI), higher BMD, lower osteoporosis prevalence, and fewer prior fractures than women from the general population or women with breast cancer without AI use (all

conclusionHigher baseline BMI, BMD, and lower prevalence of prior fracture at baseline may offset the adverse effects of AI exposure. Although confirmatory data from large cohort studies are required, our findings challenge the view that all women with breast cancer initiating AI therapy should be considered at high risk for fractures. IMPLICATIONS FOR PRACTICE: In a population-based observational registry that included 1,775 patients initiating long-term aromatase inhibitor therapy, risk for major osteoporotic fracture, hip fracture, or any fracture was similar to the general population. Higher baseline body mass index, bone mineral density, and lower prevalence of prior fracture at baseline may offset the adverse effects of aromatase inhibitor exposure.

Indexed as

AgedAromatase InhibitorsBone DensityBreast NeoplasmsCanadaCase-Control StudiesChemotherapy, AdjuvantFemaleFollow-Up StudiesFractures, BoneHumansLongitudinal StudiesOsteoporosisPrevalencePrognosisRegistriesAromatase InhibitorsAromatase inhibitorsBone densityBreast cancerFractureOsteoporosis

Identifiers

PMID31292269
PMCPMC6853130
OpenAlexW2961237381

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.