Evidence map›Paper›PMID 41543881›Full record

ArticleThe journal of pathology. Clinical research2026

Alcian blue-positive stromal phenotype in basal cell carcinoma is associated with progression on first-line hedgehog inhibitors.

Viola K DeTemple, Rudolf Stadler, Sabine Bredemeier, Sungyoung Chung, Katrin Schaper-Gerhardt, Mareike Alter, Yenny Angela, Henner Stege, Ulrike Leiter, Jan Ohletz and 8 more

Abstract readMulticenter Study
In one paragraph

Article in The journal of pathology. Clinical research, 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

18 authors.

Viola K DeTempleDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.ORCID https://orcid.org/0000-0001-6246-8862
Rudolf StadlerDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Sabine BredemeierDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Sungyoung ChungDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Katrin Schaper-GerhardtDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Mareike AlterDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Yenny AngelaDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Henner StegeDepartment of Dermatology, University Hospital Mainz, Mainz, Germany.
Ulrike LeiterDivision of Dermatooncology, Department of Dermatology, University Medical Center, Tuebingen, Germany.
Jan OhletzDepartment of Dermatology, Vivantes MVZ GmbH, Berlin-Spandau, Germany.
Elisabeth LivingstoneDepartment of Dermatology, University Hospital Essen, Essen, Germany.
Imke von WasielewskiSkin Cancer Center Hannover, Department of Dermatology and Allergy, Hannover Medical School, Hannover, Germany.
Jessica C HasselMedical Faculty Heidelberg, Department of Dermatology and National Center for Tumour Diseases (NCT), NCT Heidelberg, Heidelberg University, Heidelberg, Germany.
Julia HuynhDepartment of Dermatology, Charité - University Hospital Berlin, Berlin, Germany.
Christoffer GebhardtSkin Cancer Center, Department of Dermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Claudia PföhlerDepartment of Dermatology, Saarland University Hospital and Saarland University Faculty of Medicine, Homburg, Germany.
Ralf GutzmerDepartment of Dermatology, Johannes Wesling Medical Center Minden, Ruhr-University Bochum, Bochum, Germany.
Christina H ScheelDepartment of Dermatology, St. Josef-Hospital Bochum, Ruhr-University Bochum, Bochum, Germany.ORCID https://orcid.org/0000-0003-0566-4650

Funding

Ruhr-Universität Bochum K181-23Ruhr-Universität Bochum K181-24
6 · The paper itself

Abstract

Basal cell carcinoma (BCC) is the most frequent malignancy in fair-skinned populations. Although curable in most cases, approximately 4% of patients develop locally advanced or metastatic disease (advBCC) requiring systemic therapy. Hedgehog pathway inhibitors (HHIs; vismodegib/sonidegib) constitute standard first-line treatment, yet individual responses vary and no histopathological biomarker predicting therapeutic outcome exists. We conducted a retrospective, multicenter analysis of 70 BCCs encompassing clinically common and advanced stages. Routine hematoxylin and eosin and Alcian blue (AB; pH 2.5) staining was evaluated using a 17-parameter, numerically encoded histopathology matrix spanning tumor morphology, stromal composition, and immune contexture. Data were mapped by unsupervised hierarchical clustering. Distinct AB staining patterns were observed: superficial and nodular BCCs typically exhibited an AB-positive peritumoral border, whereas infiltrative and sclerosing subtypes displayed a diffuse AB-positive desmoplastic stroma. The latter also correlated with advanced EADO clinical stages (correlation coefficients 0.46-0.48; p < 0.001). In a subset of 30 advBCCs obtained before or during HHI therapy, AB-positive stroma was the only parameter independently associated with shorter progression-free survival (multivariable hazard ratio = 23.8; 95% CI 4.02-141.3; p < 0.001). Established clinical or histological features failed to associate with outcome. Our findings identify diffuse AB-positive stroma as a readily detectable feature of histologically aggressive BCC and as a candidate biomarker associated with progression under HHI treatment. Because AB staining is routine, inexpensive, and easily standardized, this phenotype represents an immediately implementable readout for prospective validation and a potential link between extracellular-matrix remodeling and therapy resistance in BCC.

Indexed as

AnilidesAntineoplastic AgentsBasal Cell CarcinomaHedgehog ProteinsPyridinesSkin NeoplasmsStromal CellsAgedAged, 80 and overAlcian BlueBiomarkers, TumorBiphenyl CompoundsDisease ProgressionFemaleHumansMaleAlcian BlueAnilidesAntineoplastic AgentsBiomarkers, TumorBiphenyl CompoundsHedgehog ProteinsHhAntag691PyridinessonidegibAlcian blue stainingbasal cell carcinomabiomarkersdesmoplasiaglycosaminoglycanshedgehog inhibitorssonidegibtherapy resistancetumor stromavismodegib

Identifiers

PMID41543881
PMCPMC12810521

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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.