Evidence map›Paper›PMID 42081023›Full record

ArticleAnnals of surgical oncology2026

Predictive Value of Routine Imaging for the Diagnosis of Pathologic Complete Response After Neoadjuvant Chemotherapy in Breast Cancer.

Maria Müller, Jörg Heil, André Pfob, Lie Cai, Eva Reisig, Riku Togawa, André Hennigs, Fabian Riedel, Anne Stieber, Manuel Feisst and 6 more

Abstract read
In one paragraph

Article in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

16 authors.

Maria MüllerBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Jörg HeilBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany. joerg.heil@kse-hd.de.
André PfobBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Lie CaiBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Eva ReisigBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Riku TogawaBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
André HennigsBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Fabian RiedelBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Anne StieberDepartment of Diagnostic and Interventional Radiology, Heidelberg University Hospital, Heidelberg, Germany.
Manuel FeisstInstitute of Medical Biometry (IMBI), Heidelberg University, Heidelberg, Germany.
Juliane NeesBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Andreas SchneeweissNational Center for Tumor Diseases, University Hospital and German Cancer Research Center Heidelberg, Heidelberg, Germany.
Peter SinnInstitute of Pathology, University of Heidelberg, Heidelberg, Germany.
Oliver ZivanovicBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Michael GolattaBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Benedikt SchäfgenBreast Unit, Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfter neoadjuvant chemotherapy (NACT) of breast cancer, an accurate response assessment is essential for the de-escalation of surgical therapy. This study evaluated whether breast imaging procedures can reliably predict a pathologic complete response (pCR).

methodsThis retrospective, monocenter study included 388 cases of invasive breast cancer treated by NACT. Most of the patients received mammography (MG) and ultrasound (US). In some cases, magnetic resonance imaging (MRI) was performed for special indications. The absence of residual tumor on imaging was defined as clinical complete response (cCR). Minimal signs of residual tumor were categorized as near-cCR. The primary endpoints were negative predictive values (NPVs) and false-negative rates (FNRs) of all imaging methods, combined and separately, for the whole cohort and subgroups of triple-negative (TN), human epidermal growth factor 2-positive (HER2+), and hormone receptor-positive (HR+)/HER2- breast cancer.

resultsThe overall pCR rate was 40.7 %, with most pCR cases having triple-negative breast cancer (TNBC) (n = 85, 57.8 %). The highest NPV (71.6 %) and the lowest FNR (11.0 %) in the overall cohort were achieved by the combination of ultrasound and mammography. In the TNBC subgroup, NPVs ranged from 78.1 % to 83.7 %, compared with lower NPVs in the HR+ subgroup (34.2-50.0 %). If near-cCR cases were defined together with cCR as a "negative" test result, the predictive accuracy of imaging decreased in the whole cohort (FNR, 34.8 %; NPV, 56.1 %).

conclusionStandard imaging is insufficient to predict pCR reliably in an unselected cohort. Strict patient selection and additional diagnostics are necessary for safe confirmation of pCR.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCarcinoma, Ductal, BreastMagnetic Resonance ImagingMammographyNeoadjuvant TherapyUltrasonography, MammaryAdultAgedCarcinoma, LobularChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansMiddle AgedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneBreast cancerMammographyNeoadjuvant chemotherapyPathological responsePredictionRoutine imagingUltrasound

Identifiers

PMID42081023
PMCPMC13337868

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.