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  1. Pubblicazioni

Histologic subtyping affecting outcome of triple negative breast cancer: a large Sardinian population-based analysis

Articolo
Data di Pubblicazione:
2020
Citazione:
Histologic subtyping affecting outcome of triple negative breast cancer: a large Sardinian population-based analysis / Sanges, Francesca; Floris, Matteo; Cossu-Rocca, Paolo; Muroni, Maria R.; Pira, Giovanna; Urru, Silvana Anna Maria; Barrocu, Renata; Gallus, Silvano; Bosetti, Cristina; D’Incalci, Maurizio; Manca, Alessandra; Uras, Maria Gabriela; Medda, Ricardo; Sollai, Elisabetta; Murgia, Alma; Palmas, Dolores; Atzori, Francesco; Zinellu, Angelo; Cambosu, Francesca; Moi, Tiziana; Ghiani, Massimo; Marras, Vincenzo; Santona, Maria Cristina; Canu, Luisa; Valle, Enrichetta; Sarobba, Maria Giuseppina; Onnis, Daniela; Asunis, Anna; Cossu, Sergio; Orrù, Sandra; De Miglio, Maria Rosaria. - In: BMC CANCER. - ISSN 1471-2407. - 20:1(2020), pp. 1-14. [10.1186/s12885-020-06998-9]
Abstract:
Background
Triple Negative breast cancer (TNBC) includes a heterogeneous group of tumors with different clinico-pathological features, molecular alterations and treatment responsivity. Our aim was to evaluate the clinico-pathological heterogeneity and prognostic significance of TNBC histologic variants, comparing “special types” to high-grade invasive breast carcinomas of no special type (IBC-NST).

Methods
This study was performed on data obtained from TNBC Database, including pathological features and clinical records of 1009 TNBCs patients diagnosed between 1994 and 2015 in the four most important Oncology Units located in different hospitals in Sardinia, Italy. Kaplan-Meier analysis, log-rank test and multivariate Cox proportional-hazards regression were applied for overall survival (OS) and disease free survival (DFS) according to TNBC histologic types.

Results
TNBC “special types” showed significant differences for several clinico-pathological features when compared to IBC-NST. We observed that in apocrine carcinomas as tumor size increased, the number of metastatic lymph nodes manifestly increased. Adenoid cystic carcinoma showed the smallest tumor size relative to IBC-NST. At five-year follow-up, OS was 92.1, 100.0, and 94.5% for patients with apocrine, adenoid cystic and medullary carcinoma, respectively; patients with lobular and metaplastic carcinoma showed the worst OS, with 79.7 and 84.3%, respectively. At ten-years, patients with adenoid cystic (100.0%) and medullary (94.5%) carcinoma showed a favourable prognosis, whereas patients with lobular carcinoma showed the worst prognosis (73.8%). TNBC medullary type was an independent prognostic factor for DFS compared to IBC-NST.

Conclusions
Our study confirms that an accurate and reliable histopathologic definition of TNBC subtypes has a significant clinical utility and is effective in the therapeutic decision-making process, with the aim to develop innovative and personalized treatments.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Triple negative breast cancer, Clinico-pathological features, Prognosis, Histologic special type, Tumor size, Metastatic lymph node
Elenco autori:
Sanges, Francesca; Floris, Matteo; Cossu-Rocca, Paolo; Muroni, Maria R.; Pira, Giovanna; Urru, Silvana Anna Maria; Barrocu, Renata; Gallus, Silvano; Bosetti, Cristina; D’Incalci, Maurizio; Manca, Alessandra; Uras, Maria Gabriela; Medda, Ricardo; Sollai, Elisabetta; Murgia, Alma; Palmas, Dolores; Atzori, Francesco; Zinellu, Angelo; Cambosu, Francesca; Moi, Tiziana; Ghiani, Massimo; Marras, Vincenzo; Santona, Maria Cristina; Canu, Luisa; Valle, Enrichetta; Sarobba, Maria Giuseppina; Onnis, Daniela; Asunis, Anna; Cossu, Sergio; Orrù, Sandra; De Miglio, Maria Rosaria
Autori di Ateneo:
COSSU ROCCA Paolo Alessandro
DE MIGLIO Maria Rosaria
MURONI Maria Rosaria
URAS Maria Gabriela
ZINELLU Angelo
Link alla scheda completa:
https://iris.uniss.it/handle/11388/234412
Link al Full Text:
https://iris.uniss.it//retrieve/handle/11388/234412/164976/Histologic%20subtyping%20affecting%20outcome%20of.pdf
Pubblicato in:
BMC CANCER
Journal
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URL

https://bmccancer.biomedcentral.com/articles/10.1186/s12885-020-06998-9#citeas
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