Pubblicazioni

PTEN Loss as a Predictor of Tumor Heterogeneity and Poor Prognosis in Patients With EGFR-mutant Advanced Non-small-cell Lung Cancer Receiving Tyrosine Kinase Inhibitors  (2021)

Autori:
Ferrara, Miriam Grazia; Martini, Maurizio; D'Argento, Ettore; Forcella, Chiara; Vita, Emanuele; Di Noia, Vincenzo; Sperduti, Isabella; Bilotta, Mirna; Ribelli, Marta; Damiano, Paola; Cannella, Antonella; Stefani, Alessio; Pilotto, Sara; Carbone, Carmine; Piro, Geny; Milella, Michele; Tortora, Giampaolo; Bria, Emilio
Titolo:
PTEN Loss as a Predictor of Tumor Heterogeneity and Poor Prognosis in Patients With EGFR-mutant Advanced Non-small-cell Lung Cancer Receiving Tyrosine Kinase Inhibitors
Anno:
2021
Tipologia prodotto:
Articolo in Rivista
Tipologia ANVUR:
Articolo su rivista
Lingua:
Inglese
Formato:
A Stampa
Referee:
No
Nome rivista:
CLINICAL LUNG CANCER
ISSN Rivista:
1525-7304
N° Volume:
22
Numero o Fascicolo:
4
Intervallo pagine:
351-360
Parole chiave:
Afatinib; Erlotinib; Gefitinib; IGFR; MET; Osimertinib; p53; Adult; Aged; Aged, 80 and over; Carcinoma, Non-Small-Cell Lung; Disease Progression; ErbB Receptors; Female; Humans; Immunohistochemistry; Lung Neoplasms; Male; Middle Aged; Mutation; PTEN Phosphohydrolase; Prognosis; Progression-Free Survival; Protein Kinase Inhibitors; Reproducibility of Results; Retrospective Studies; Survival Rate
Breve descrizione dei contenuti:
Background: Rapid disease progression of patients with advanced epidermal growth factor receptor (EGFR)-mutant non-small-cell lung cancer (NSCLC) has been recently associated with tumor heterogeneity, which may be mirrored by coexisting concomitant alterations. The aim of this analysis was to investigate the correlation between loss of function of PTEN and the efficacy of tyrosine kinase inhibitors in this population. Materials and Methods: Archival tumor blocks from patients with EGFR-mutant NSCLC who were administered upfront tyrosine kinase inhibitors were retrospectively collected. The status of 4 genes (PTEN, TP53, c-MET, IGFR) was evaluated by immunohistochemistry, and it was correlated with overall response rate, overall survival (OS), and progression-free survival (PFS). Results: Fifty-one patients were included. In multivariate analysis, PTEN loss (hazard ratio [HR], 3.46; 95% confidence interval [CI], 1.56-7.66; P = .002), IGFR overexpression (HR, 2.22; 95% CI, 1.03-4.77; P = .04), liver metastases (HR, 3.55; 95% CI, 1.46-8.65; P = .005), and Eastern Cooperative Oncology Group performance status (ECOG PS) > 1 (HR, 2.57; 95% CI, 1.04-6.34; P = .04) were significantly associated with shorter PFS. Patients with PTEN loss had a median PFS of 6 months (2-year PFS, 11.6%), whereas patients without PTEN loss had a median PFS of 18 months (2-year PFS, 43.6%) (log-rank P < .005). In the multivariate analysis, PTEN loss (HR, 5.92; 95% CI, 2.37-14.81; P < .005), liver metastases (HR, 2.63; 95% CI, 1.06-6.51; P = .037), and ECOG PS > 1 (HR, 2.80; 95% CI, 1.15-6.81; P = .024) were significantly associated with shorter OS. Patients with PTEN loss had a median OS of 6 months (2-year OS, 12.2%), whereas in patients without PTEN loss, OS was not reached (2-year OS, 63.9%) (log-rank P < .0005).Conclusions: A low-cost and reproducible immunohistochemistry assay for PTEN loss analysis represents a potential tool for identifying tumor heterogeneity in patients with advanced EGFR-mutant NSCLC.
Id prodotto:
126255
Handle IRIS:
11562/1063754
ultima modifica:
17 novembre 2022
Citazione bibliografica:
Ferrara, Miriam Grazia; Martini, Maurizio; D'Argento, Ettore; Forcella, Chiara; Vita, Emanuele; Di Noia, Vincenzo; Sperduti, Isabella; Bilotta, Mirna; Ribelli, Marta; Damiano, Paola; Cannella, Antonella; Stefani, Alessio; Pilotto, Sara; Carbone, Carmine; Piro, Geny; Milella, Michele; Tortora, Giampaolo; Bria, Emilio, PTEN Loss as a Predictor of Tumor Heterogeneity and Poor Prognosis in Patients With EGFR-mutant Advanced Non-small-cell Lung Cancer Receiving Tyrosine Kinase Inhibitors «CLINICAL LUNG CANCER» , vol. 22 , n. 42021pp. 351-360

Consulta la scheda completa presente nel repository istituzionale della Ricerca di Ateneo IRIS

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