Evidence map›Paper›PMID 42390022›Full record

ArticleHistopathology2026

TROP2 immunoreactivity in pulmonary large cell neuroendocrine carcinoma.

Michael Minkley, Kashif Ravasia, Thi Nghiem, Dongxia Gao, Jamie Feng, Andrew Churg, Julia R Naso

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Article in Histopathology, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Michael MinkleyDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0003-1602-5096
Kashif RavasiaUndergraduate Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Thi NghiemDepartment of Clinical Research, BC Cancer, Vancouver, British Columbia, Canada.
Dongxia GaoDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Jamie FengDepartment of Medical Oncology, BC Cancer, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0009-0002-3017-1567
Andrew ChurgDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0002-4851-8517
Julia R NasoDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0002-7799-7860

Funding

This project received funding from the University of British Columbia Diagnostic and Molecular Pathology Residency Program.
6 · The paper itself

Abstract

introductionTROP2 antibody-drug conjugates have shown promising anti-tumour activity, but neither the activity of these agents nor TROP2 expression has been well studied in pulmonary large cell neuroendocrine carcinoma (LCNEC), a rare and aggressive cancer type. We aimed to (i) determine the prevalence of TROP2 immunoreactivity in LCNEC; (ii) assess whether TROP2 immunoreactivity in LCNEC is related to RB1 loss on IHC or to the presence of NSCLC or SCLC components and (iii) determine whether TROP2 immunoreactivity in LCNEC has prognostic significance.

methodsTROP2 immunohistochemistry was performed on 58 pure LCNECs and 25 areas of LCNEC that were combined with other carcinomas, in tissue microarray format. TROP2 was scored for the percent of tumour cells staining, and with evaluation of cytoplasmic versus membranous staining, approximating a previously published predictive scoring method.

resultsTROP2 staining in ≥1% and ≥50% of LCNEC cells was present in 60% and 26% of pure LCNEC tumours, respectively. Cytoplasmic-type staining, previously implicated in greater antibody-drug conjugate response, was present in 48% of pure LCNEC cases. Positive TROP2 staining was less frequent in pure LCNEC than in the LCNEC component of tumours that also contained a NSCLC component (≥1%: P = 0.0087; ≥50%: P = 0.011), and ≥50% TROP2 staining in pure LCNEC was associated with retained RB1 staining on immunohistochemistry (P = 0.032). TROP2 staining was not associated with recurrence-free survival or disease-specific survival outcomes.

conclusionFrequently positive TROP2 IHC suggests that TROP2 antibody-drug conjugates may be potential treatments for LCNEC.

Indexed as

Antigens, NeoplasmBiomarkers, TumorCarcinoma, Large CellCarcinoma, NeuroendocrineCell Adhesion MoleculesLung NeoplasmsAdultAgedAged, 80 and overFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesTACSTD2 protein, humanbiomarkerslarge cell neuroendocrine carcinomapathologyRB1TROP2

Identifiers

PMID42390022
PMCPMC13643618

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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.