Ascl1 and OTP tumour expressions are associated with disease-free survival in lung atypical carcinoids.


Journal

Histopathology
ISSN: 1365-2559
Titre abrégé: Histopathology
Pays: England
ID NLM: 7704136

Informations de publication

Date de publication:
May 2023
Historique:
revised: 11 01 2023
received: 21 10 2022
accepted: 28 01 2023
medline: 4 4 2023
pubmed: 1 2 2023
entrez: 31 1 2023
Statut: ppublish

Résumé

According to World Health Organization guidelines, atypical carcinoids (ACs) are well-differentiated lung neuroendocrine tumours with 2-10 mitoses/2 mm

Identifiants

pubmed: 36720841
doi: 10.1111/his.14873
doi:

Substances chimiques

Ki-67 Antigen 0
ASCL1 protein, human 0
Basic Helix-Loop-Helix Transcription Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

870-884

Subventions

Organisme : Italian Ministry of Health
ID : ERP-2017-23671129
Organisme : Integrative Molecular Analysis of Pure and Combined Lung Large Cell Neuroendocrine Carcinoma (LCNEC)
Organisme : Italian Ministry of Health with Ricerca Corrente
Organisme : FIRC-AIRC

Informations de copyright

© 2023 The Authors. Histopathology published by John Wiley & Sons Ltd.

Références

World HO. Thoracic tumors. Lyon, France. Geneva, Switzerland: International Agency for Research on Cancer. Print copies are distributed by WHO Press, World Health Organization, 2021 xiii, 565 pages: illustrations (color, black and white).
Baudin E, Hayes AR, Scoazec JY et al. Unmet medical needs in pulmonary neuroendocrine (carcinoid) neoplasms. Neuroendocrinology 2019; 108; 7-17.
Huang Y, Yang X, Lu T et al. Assessment of the prognostic factors in patients with pulmonary carcinoid tumor: a population-based study. Cancer Med. 2018; 7; 2434-2441.
Caplin ME, Baudin E, Ferolla P et al. Pulmonary neuroendocrine (carcinoid) tumors: European neuroendocrine tumor society expert consensus and recommendations for best practice for typical and atypical pulmonary carcinoids. Ann. Oncol. 2015; 26; 1604-1620.
Jiang SX, Kameya T, Asamura H et al. Hash1 expression is closely correlated with endocrine phenotype and differentiation extent in pulmonary neuroendocrine tumors. Mod. Pathol. 2004; 17; 222-229.
Moonen L, Derks J, Dingemans AM, Speel EJ. Orthopedia homeobox (otp) in pulmonary neuroendocrine tumors: the diagnostic value and possible molecular interactions. Cancers (Basel) 2019; 1508; 11.
Marchio C, Gatti G, Massa F et al. Distinctive pathological and clinical features of lung carcinoids with high proliferation index. Virchows Arch. 2017; 471; 713-720.
Nagtegaal ID, Odze RD, Klimstra D et al. The 2019 who classification of tumours of the digestive system. Histopathology 2020; 76; 182-188.
Volante M, Brizzi MP, Faggiano A et al. Somatostatin receptor type 2a immunohistochemistry in neuroendocrine tumors: a proposal of scoring system correlated with somatostatin receptor scintigraphy. Mod. Pathol. 2007; 20; 1172-1182.
Rindi G, Klersy C, Inzani F et al. Grading the neuroendocrine tumors of the lung: an evidence-based proposal. Endocr. Relat. Cancer 2014; 21; 1-16.
Prinzi N, Rossi RE, Proto C et al. Recent advances in the management of typical and atypical lung carcinoids. Clin. Lung Cancer 2021; 22; 161-169.
Castro DS, Martynoga B, Parras C et al. A novel function of the proneural factor ascl1 in progenitor proliferation identified by genome-wide characterization of its targets. Genes Dev. 2011; 25; 930-945.
Altree-Tacha D, Tyrrell J, Li F. Mash1 is highly specific for neuroendocrine carcinomas: an immunohistochemical evaluation on normal and various neoplastic tissues. Arch. Pathol. Lab. Med. 2017; 141; 288-292.
Ye B, Cappel J, Findeis-Hosey J et al. Hash1 is a specific immunohistochemical marker for lung neuroendocrine tumors. Hum. Pathol. 2016; 48; 142-147.
Laddha SV, da Silva EM, Robzyk K et al. Integrative genomic characterization identifies molecular subtypes of lung carcinoids. Cancer Res. 2019; 79; 4339-4347.
Borromeo MD, Savage TK, Kollipara RK et al. Ascl1 and neurod1 reveal heterogeneity in pulmonary neuroendocrine tumors and regulate distinct genetic programs. Cell Rep. 2016; 16; 1259-1272.
Baine MK, Hsieh MS, Lai WV et al. Sclc subtypes defined by ascl1, neurod1, pou2f3, and yap1: a comprehensive immunohistochemical and histopathologic characterization. J. Thorac. Oncol. 2020; 15; 1823-1835.
Nonaka D, Papaxoinis G, Mansoor W. Diagnostic utility of orthopedia homeobox (otp) in pulmonary carcinoid tumors. Am. J. Surg. Pathol. 2016; 40; 738-744.
Alcala N, Leblay N, Gabriel AAG et al. Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids. Nat. Commun. 2019; 10; 3407.
Swarts DR, Henfling ME, Van Neste L et al. Cd44 and otp are strong prognostic markers for pulmonary carcinoids. Clin. Cancer Res. 2013; 19; 2197-2207.
Papaxoinis G, Nonaka D, O'Brien C, Sanderson B, Krysiak P, Mansoor W. Prognostic significance of cd44 and orthopedia homeobox protein (otp) expression in pulmonary carcinoid tumours. Endocr. Pathol. 2017; 28; 60-70.
Derks JL, Rijnsburger N, Hermans BCM et al. Clinical-pathologic challenges in the classification of pulmonary neuroendocrine neoplasms and targets on the horizon for future clinical practice. J. Thorac. Oncol. 2021; 16; 1632-1646.
Clay V, Papaxoinis G, Sanderson B et al. Evaluation of diagnostic and prognostic significance of ki-67 index in pulmonary carcinoid tumours. Clin. Transl. Oncol. 2017; 19; 579-586.
Oka N, Kasajima A, Konukiewitz B et al. Classification and prognostic stratification of bronchopulmonary neuroendocrine neoplasms. Neuroendocrinology 2020; 110; 393-403.
Dermawan JKT, Farver CF. The role of histologic grading and ki-67 index in predicting outcomes in pulmonary carcinoid tumors. Am. J. Surg. Pathol. 2020; 44; 224-231.
Centonze G, Maisonneuve P, Simbolo M et al. Lung carcinoid tumors: Histology and ki-67, the eternal rivalry. Histopathology 2022; 82; 324-339.
Hermans BCM, Derks JL, Moonen L et al. Pulmonary neuroendocrine neoplasms with well differentiated morphology and high proliferative activity: Illustrated by a case series and review of the literature. Lung Cancer 2020; 150; 152-158.
IARC. World Health Organization classification of tumours 1. Digestive system tumours. 1.1 ed. Lyon: IARC, 2019; 635.

Auteurs

Giovanni Centonze (G)

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Tumor Genomics Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Patrick Maisonneuve (P)

Division of Epidemiology and Biostatistics, IEO, European Institute of Oncology IRCCS, Milan, Italy.

Michele Simbolo (M)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Vincenzo Lagano (V)

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Federica Grillo (F)

Unit of Pathology, Department of Surgical Sciences and Integrated Diagnostics, University of Genoa and Ospedale Policlinico San Martino, Genoa, Italy.

Natalie Prinzi (N)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Sara Pusceddu (S)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Loretta Missiato (L)

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Marilena Colantuono (M)

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Giovanna Sabella (G)

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Luisa Bercich (L)

Department of Pathology, ASST Spedali Civili of Brescia, Brescia, Italy.

Alessandro Mangogna (A)

Institute for Maternal and Child Health, IRCCS Burlo Garofalo, Trieste, Italy.

Luigi Rolli (L)

Thoracic Surgery Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.

Salvatore Grisanti (S)

Medical Oncology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, ASST Spedali Civili, Brescia, Italy.

Mauro Roberto Benvenuti (MR)

Thoracic Surgery Unit, Department of Medical and Surgical Specialties Radiological Sciences and Public Health, Medical Oncology, University of Brescia, ASST Spedali Civili of Brescia, Brescia, Italy.

Ugo Pastorino (U)

Thoracic Surgery Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.

Luca Roz (L)

Tumor Genomics Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Aldo Scarpa (A)

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
ARC-NET Research Center for Applied Research on Cancer, and Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Alfredo Berruti (A)

Medical Oncology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, ASST Spedali Civili, Brescia, Italy.

Carlo Capella (C)

Unit of Pathology, Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Massimo Milione (M)

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

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