Evidence map›Paper›PMID 42275912›Full record

ArticleBreast (Edinburgh, Scotland)2026

Case-mix-adjusted benchmarking of long-term breast cancer-specific mortality: Insights from a nationwide Swedish registry.

Jacob Thurell, Iurii Petrov, Peter Lindgren, Jonas Bergh, Irma Fredriksson, Narsis A Kiani, Elham Hedayati

Abstract read
In one paragraph

Article in Breast (Edinburgh, Scotland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jacob ThurellDepartment of Oncology-Pathology, Karolinska Institutet, Anna Steckséns Gata 30A, D2:04, Solna, 171 64, Sweden; Breast Cancer Center, Department of Breast, Endocrine Tumours and Sarcoma, Karolinska Comprehensive Cancer Center, Karolinska University Hospital, Eugeniavägen 3, Stockholm, 171 76, Sweden. Electronic address: jacob.thurell@ki.se.
Iurii PetrovDepartment of Microbiology, Tumor- and Cell Biology, Karolinska Institutet, Solnavägen 9, Solna, 171 65, Sweden; Cancer Centrum Karolinska, Visionsgatan 56b, Stockholm, 171 76, Sweden; Division of Medical Diagnostics, Radiology, Karolinska University Hospital, C1:46, Stockholm, 141 86, Sweden.
Peter LindgrenDepartment of Learning, Informatics, Management and Ethics, Karolinska, Institutet, Tomtebodavägen 18 A, Floor 4, Stockholm, 171 77, Sweden; The Swedish Institute for Health Economics, Råbygatan 2, Lund, 223 61, Sweden.
Jonas BerghDepartment of Oncology-Pathology, Karolinska Institutet, Anna Steckséns Gata 30A, D2:04, Solna, 171 64, Sweden; Breast Cancer Center, Department of Breast, Endocrine Tumours and Sarcoma, Karolinska Comprehensive Cancer Center, Karolinska University Hospital, Eugeniavägen 3, Stockholm, 171 76, Sweden.
Irma FredrikssonBreast Cancer Center, Department of Breast, Endocrine Tumours and Sarcoma, Karolinska Comprehensive Cancer Center, Karolinska University Hospital, Eugeniavägen 3, Stockholm, 171 76, Sweden; Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, (L1:00), Stockholm, 171 76, Sweden.
Narsis A KianiDepartment of Oncology-Pathology, Karolinska Institutet, Anna Steckséns Gata 30A, D2:04, Solna, 171 64, Sweden; Algorithmic Dynamics Lab, Center for Molecular Medicine, Karolinska Instiutet, Visionsgatan 18, Solna, 171 64, Sweden.
Elham HedayatiDepartment of Oncology-Pathology, Karolinska Institutet, Anna Steckséns Gata 30A, D2:04, Solna, 171 64, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMeaningful comparisons of breast cancer (BC) survival across hospitals require appropriate case-mix adjustment. While such adjustment is routine for short-term outcomes, it remains less established for long-term BC-specific mortality (BCSM). We developed case-mix models to evaluate whether robust hospital-level benchmarking of 10-year BCSM can be achieved using routinely collected registry data.

methodsUsing the nationwide Swedish BC registry linked to population registers, we developed full and reduced logistic regression models for 10-year BCSM. The full model included age, tumour, socioeconomic, and comorbidity variables while the reduced model used routinely collected age and tumour variables. Model performance was assessed via discrimination and calibration. The model impact on hospital benchmarking was evaluated through observed-to-expected mortality ratios at the hospital level, comparing expected mortality estimates and shifts in outlier status.

resultsThe study included 10,888 patients. Age, stage, and grade were the strongest predictors, while comorbidity and socioeconomic variables added limited incremental predictive value. Both the full and reduced 10-year BCSM models demonstrated similar discrimination and near-perfect calibration. Furthermore, the full and reduced models yielded highly comparable expected mortality rates across 12 hospitals (mean absolute difference 0.6 percentage points), with consistent identification of hospital outliers in all but one hospital.

conclusionsRoutinely collected data on age and tumour characteristics appear to offer a feasible foundation for fair benchmarking of long-term BCSM in a publicly-funded healthcare system. While external validation in contemporary and international cohorts is an important next step, these findings might be relevant to other countries with strong cancer registry infrastructure.

Indexed as

BenchmarkingBreast NeoplasmsAdultAgedAged, 80 and overAge FactorsComorbidityDiagnosis-Related GroupsFemaleHumansLogistic ModelsMiddle AgedRegistriesRisk AdjustmentSwedenBreast cancerCancer survivalCase-mix adjustmentHospital benchmarkingLong-term outcomesNational cancer registryPopulation-based studyQuality improvementReal-world dataRisk prediction model

Identifiers

PMID42275912
PMCPMC13272560

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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.