A Multimodal Biomarker Predicts Dissemination of Bronchial Carcinoid.

Ki-67 distant metastases immunohistochemistry prognosis pulmonary carcinoid

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 Jun 2022
Historique:
received: 01 06 2022
revised: 22 06 2022
accepted: 26 06 2022
entrez: 9 7 2022
pubmed: 10 7 2022
medline: 10 7 2022
Statut: epublish

Résumé

Background: Curatively treated bronchial carcinoid tumors have a relatively low metastatic potential. Gradation into typical (TC) and atypical carcinoid (AC) is limited in terms of prognostic value, resulting in yearly follow-up of all patients. We examined the additional prognostic value of novel immunohistochemical (IHC) markers to current gradation of carcinoids. Methods: A retrospective single-institution cohort study was performed on 171 patients with pathologically diagnosed bronchial carcinoid (median follow-up: 66 months). The risk of developing distant metastases based on histopathological characteristics (Ki-67, p16, Rb, OTP, CD44, and tumor diameter) was evaluated using multivariate regression analysis and the Kaplan−Meier method. Results: Of 171 patients, seven (4%) had disseminated disease at presentation, and 164 (96%) received curative-intent treatment with either endobronchial treatment (EBT) (n = 61, 36%) or surgery (n = 103, 60%). Among the 164 patients, 13 developed metastases at follow-up of 81 months (IQR 45−162). Univariate analysis showed that Ki-67, mitotic index, OTP, CD44, and tumor diameter were associated with development of distant metastases. Multivariate analysis showed that mitotic count, Ki-67, and OTP were independent risk factors for development of distant metastases. Using a 5% cutoff for Ki-67, Kaplan−Meier analysis showed that the risk of distant metastasis development was significantly associated with the number of risk predictors (AC, Ki-67 ≥ 5%, and loss of OTP or CD44) (p < 0.0001). Six out of seven patients (86%) with all three positive risk factors developed distant metastasis. Conclusions: Mitotic count, proliferation index, and OTP IHC were independent predictors of dissemination at follow-up. In addition to the widely used carcinoid classification, a comprehensive analysis of histopathological variables including Ki-67, OTP, and CD44 could assist in the determination of distant metastasis risks of bronchial carcinoids.

Identifiants

pubmed: 35805004
pii: cancers14133234
doi: 10.3390/cancers14133234
pmc: PMC9265109
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Ann Thorac Surg. 2013 Oct;96(4):1156-1162
pubmed: 23915584
Hum Pathol. 2003 Feb;34(2):136-42
pubmed: 12612881
Eur J Cardiothorac Surg. 2011 Apr;39(4):565-9
pubmed: 20888248
Am J Pathol. 1997 Feb;150(2):393-400
pubmed: 9033254
Lung Cancer Int. 2015;2015:545601
pubmed: 26770831
Cancer. 2008 Jul 1;113(1):5-21
pubmed: 18473355
Lung Cancer. 2019 Aug;134:85-95
pubmed: 31320001
Am J Surg Pathol. 2020 Feb;44(2):224-231
pubmed: 31490236
Endocr Pathol. 2022 Mar;33(1):115-154
pubmed: 35294740
J Thorac Oncol. 2014 Mar;9(3):273-84
pubmed: 24518085
Virchows Arch. 2006 Oct;449(4):395-401
pubmed: 16967267
Mod Pathol. 2004 Oct;17(10):1259-67
pubmed: 15154011
Virchows Arch. 2013 May;462(5):507-13
pubmed: 23559305
PLoS One. 2014 Nov 11;9(11):e112159
pubmed: 25386659
Lung. 2017 Dec;195(6):789-798
pubmed: 29022070
Endocr Pathol. 2017 Mar;28(1):60-70
pubmed: 27873160
Endocr Relat Cancer. 2013 Dec 16;21(1):1-16
pubmed: 24344249
Ann Oncol. 2021 Apr;32(4):439-451
pubmed: 33482246
Mod Pathol. 2018 Oct;31(10):1523-1531
pubmed: 29802361
Eur J Cardiothorac Surg. 2007 Feb;31(2):186-91
pubmed: 17140801
Cancers (Basel). 2022 May 25;14(11):
pubmed: 35681581
Cancer. 2000 Feb 1;88(3):550-6
pubmed: 10649246
Clin Cancer Res. 2013 Apr 15;19(8):2197-207
pubmed: 23444222
Histopathology. 2017 Feb;70(3):412-422
pubmed: 27701763
J Clin Pathol. 2016 Jul;69(7):612-8
pubmed: 26680267
Int J Cancer. 1999 Oct 22;84(5):484-88
pubmed: 10502723
Respiration. 2018;95(4):220-227
pubmed: 29433123
Virchows Arch. 2017 Dec;471(6):713-720
pubmed: 28631159
J Cell Physiol. 2000 Mar;182(3):311-22
pubmed: 10653597

Auteurs

Ellen M B P Reuling (EMBP)

Department of Surgery, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.
Department of Surgery, Albert Schweitzer Hospital, 3318 AT Dordrecht, The Netherlands.

Dwayne D Naves (DD)

Department of Pathology, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.

Pim C Kortman (PC)

Department of Pathology, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.

Mark A M Broeckaert (MAM)

Department of Pathology, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.

Peter W Plaisier (PW)

Department of Surgery, Albert Schweitzer Hospital, 3318 AT Dordrecht, The Netherlands.

Chris Dickhoff (C)

Department of Surgery, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.
Department of Cardiothoracic Surgery, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.

Johannes M A Daniels (JMA)

Department of Pulmonary Diseases, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.

Teodora Radonic (T)

Department of Pathology, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam University Medical Center, VUMC, University Amsterdam, 1081 HV Amsterdam, The Netherlands.

Classifications MeSH