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Synaptophysin expression in V600EBRAF-mutated advanced colorectal cancers identifies a new subgroup of tumours with worse prognosis.

Authors :
Fassan, Matteo
Milione, Massimo
Maddalena, Giulia
Cremolini, Chiara
Schirripa, Marta
Pietrantonio, Filippo
Pella, Nicoletta
Dell'Aquila, Emanuela
Sperti, Elisa
Zichi, Clizia
Bergamo, Francesca
Volante, Marco
Boccaccino, Alessandra
Morano, Federica
Cortiula, Francesco
De Maglio, Giovanna
Rimassa, Lorenza
Smiroldo, Valeria
Calvetti, Lorenzo
Aprile, Giuseppe
Source :
European Journal of Cancer. Mar2021, Vol. 146, p145-154. 10p.
Publication Year :
2021

Abstract

Neuroendocrine differentiation has been extensively associated with worse prognosis and to mechanisms of therapy resistance in several epithelial cancers. A high prevalence of neuroendocrine differentiation was recently described in V600E BRAF- mutated (BRAF mt) metastatic colorectal cancers (mCRCs) but no data are available about its prognostic impact in this setting. We assessed synaptophysin immunohistochemical expression in a multi-institutional series of 159 BRAF mt mCRCs with matched clinical and pathological information. Tumours were dichotomized as synaptophysin high and low. Overall survival (OS) and progression-free survival (PFS) were evaluated by Kaplan–Meier and log-rank tests. Thirty-five tumours (22.0%) showed any level of positivity for synaptophysin, and 18 (11.3%) were characterized by positivity in at least 20% of tumour cells. Four cases resulted 100% synaptophysin positive. The histotype of synaptophysin-positive tumours (i.e. ≥20%) was not otherwise specified in 11 cases (61.1%) and mucinous adenocarcinoma in 4 cases (22.2%). Four cases were DNA mismatch repair deficient (22.2%) and 7 (38.9%) were characterized by a high number of tumour-infiltrating lymphocytes. At multivariate analysis, high synaptophysin expression was a negative independent prognostic factor for both PFS (HR = 2.00, 95% confidence interval [CI] 1.21–3.33, p = 0.006) and OS (HR = 2.27, 95% CI 1.35–3.85, p = 0.001). Among BRAF mt mCRCs, synaptophysin-positive tumours are characterized by worse PFS and OS. Further studies should investigate the molecular mechanisms involved in the acquisition of the neuroendocrine phenotype to identify novel-targeted treatment strategies. • Neuroendocrine differentiation is associated with worse prognosis in several cancers. • Neuroendocrine differentiation is associated with secondary therapy resistance. • V600E BRAF colorectal cancers show high prevalence of neuroendocrine differentiation. • Synaptophysin-positive tumours are characterized by worse PFS and OS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09598049
Volume :
146
Database :
Academic Search Index
Journal :
European Journal of Cancer
Publication Type :
Academic Journal
Accession number :
149053164
Full Text :
https://doi.org/10.1016/j.ejca.2021.01.016