Abstract OBJECTIVES: To assess the independent prognostic role of histological subtypes, tumour size and lymph nodal involvement upon survival in lung neuroendocrine tumours (NETs). METHODS: A retrospective search of the database of the Department of Thoracic Surgery (Turin, Italy) identified 157 patients operated on for a newly diagnosed NET between January 1995 and December 2011. Multivariable Cox models were used to analyse predictors of overall survival and progression-free survival. RESULTS: According to histology, 71 (45.2%) were typical carcinoids (TCs), 35 (22.3%) atypical carcinoids (ACs), 37 (23.6%) large-cell neuroendocrine carcinomas (LCNCs) and 14 (8.9%) small-cell lung carcinomas (SCLCs). After a median follow-up time of 6.5 years, 60 patients died and 73 had a recurrence or died. The overall 5-, 10- and 15-year survival rates were 64%, 53% and 46%, respectively. Older age, histology (ACs, LCNCs and SCLCs vs TCs) and lymph nodal involvement were confirmed to be independent negative prognostic factors in the multivariable models for overall survival and progression-free survival. CONCLUSIONS: Tumour histology and lymph nodal involvement are definitively the predominant and relevant factors influencing survival. ACs showed an intermediate prognosis between TCs and poorly differentiated NETs.

Prognostic factors in neuroendocrine tumours of the lung: a single-centre experience / Filosso, Pier Luigi; Ruffini, Enrico; Di Gangi, S; Guerrera, Francesco; Bora, G; Ciccone, G; Galassi, C; Solidoro, P; Lyberis, P; Oliaro, Alberto; Sandri, A.. - In: EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY. - ISSN 1010-7940. - 45:3(2014), pp. 521-526. [10.1093/ejcts/ezt442]

Prognostic factors in neuroendocrine tumours of the lung: a single-centre experience

FILOSSO, Pier Luigi;
2014

Abstract

Abstract OBJECTIVES: To assess the independent prognostic role of histological subtypes, tumour size and lymph nodal involvement upon survival in lung neuroendocrine tumours (NETs). METHODS: A retrospective search of the database of the Department of Thoracic Surgery (Turin, Italy) identified 157 patients operated on for a newly diagnosed NET between January 1995 and December 2011. Multivariable Cox models were used to analyse predictors of overall survival and progression-free survival. RESULTS: According to histology, 71 (45.2%) were typical carcinoids (TCs), 35 (22.3%) atypical carcinoids (ACs), 37 (23.6%) large-cell neuroendocrine carcinomas (LCNCs) and 14 (8.9%) small-cell lung carcinomas (SCLCs). After a median follow-up time of 6.5 years, 60 patients died and 73 had a recurrence or died. The overall 5-, 10- and 15-year survival rates were 64%, 53% and 46%, respectively. Older age, histology (ACs, LCNCs and SCLCs vs TCs) and lymph nodal involvement were confirmed to be independent negative prognostic factors in the multivariable models for overall survival and progression-free survival. CONCLUSIONS: Tumour histology and lymph nodal involvement are definitively the predominant and relevant factors influencing survival. ACs showed an intermediate prognosis between TCs and poorly differentiated NETs.
2014
45
3
521
526
Prognostic factors in neuroendocrine tumours of the lung: a single-centre experience / Filosso, Pier Luigi; Ruffini, Enrico; Di Gangi, S; Guerrera, Francesco; Bora, G; Ciccone, G; Galassi, C; Solidoro, P; Lyberis, P; Oliaro, Alberto; Sandri, A.. - In: EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY. - ISSN 1010-7940. - 45:3(2014), pp. 521-526. [10.1093/ejcts/ezt442]
Filosso, Pier Luigi; Ruffini, Enrico; Di Gangi, S; Guerrera, Francesco; Bora, G; Ciccone, G; Galassi, C; Solidoro, P; Lyberis, P; Oliaro, Alberto; Sandri, A.
File in questo prodotto:
File Dimensione Formato  
accesso riservato.pdf

Accesso riservato

Dimensione 205.71 kB
Formato Adobe PDF
205.71 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1317856
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 25
  • ???jsp.display-item.citation.isi??? 27
social impact