ArticleFuture science OA2026
Side-level versus patient-level evaluation in four-view mammography classification: a comprehensive benchmark on the CMMD dataset.
Article in Future science OA, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDeep learning for mammographic image classification yields impressive performance metrics, but inconsistent evaluation methodologies-specifically whether results are reported at the independent side level or the bilateral patient level-make cross-study comparisons unreliable. The aim of this study was to quantify, on a single dataset and with a uniform training recipe, how much of the reported performance is determined by evaluation granularity rather than by model architecture. MATERIALS &
methodsWe benchmarked six backbone architectures (ResNet-18, ResNet-50, EfficientNet-B0, DenseNet-121, ConvNeXt-Tiny, ViT-B/16) crossed with three multi-view fusion strategies (concatenation, bilateral asymmetry, cross-view spatial attention) on the biopsy-confirmed Chinese Mammography Database (CMMD; 706 four-view patients), using five-fold patient-level stratified cross-validation. Sixteen configurations completed training for both binary malignancy diagnosis and five-class BI-RADS assessment. We report side-level and patient-level metrics; statistical analyses include 5-fold Wilcoxon signed-rank tests, DeLong's paired AUC test on pooled per-case scores, and bootstrap 95% confidence intervals.
resultsSide-level AUC exceeded patient-level AUC by an average of 17.5 percentage points (range 12.7-22.4), an effect that dwarfs the absolute differences observed between CNN backbones (<3 AUC points). DeLong tests resolved approximately half of all CNN-vs-CNN pairwise comparisons at p<0.05 despite small effect sizes, whereas ViT-B/16 underperformed every CNN variant by 8-10% AUC despite having 6-10× more parameters. Patient-level multi-class BI-RADS evaluation under the standard probability-averaging aggregation rule returned a degenerate macro-AUC of exactly 0.000-a property of the metric/aggregation pair, not of the models-and three concrete alternative aggregators are proposed. The extreme patient-level malignancy prevalence intrinsic to this biopsy-confirmed cohort (96.2%) rendered all models unable to identify non-malignant patients at the patient level.
conclusionReporting methodology, evaluation granularity, and dataset composition are compounding confounds in mammography classification research. Absolute performance numbers reported on CMMD should not be extrapolated to population screening settings, where prevalence is several orders of magnitude lower; studies should report both side-level and patient-level metrics with mutually consistent label/aggregation rules, and characterise performance using confidence intervals or paired statistical tests rather than fold-level Wilcoxon alone.
Indexed as
Identifiers
What OpenQuestion holds
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.