Objective: The aim of this study was to investigate everolimus efficacy in well-moderately differentiated pancreatic NEC (pNEC) G3. Methods: This was a retrospective analysis of patients with pNEC G3 and Ki67 20% to 55% treated with everolimus. Results: Fifteen patients with median Ki67 30%and Eastern Cooperative Oncology Group performance status 0 to 1 were evaluated. Of these, 4 patients received everolimus as first-line treatment, whereas 11 had been pretreated with chemotherapy or peptide receptor radionuclide therapy. Median progression-free survival was 6 months, and median overall survival was 28 months. Eleven patients achieved disease stabilization (DS) at 3 month follow-up. Six patients (40%) maintained DS for at least 12 months. Three of 4 patients who received everolimus as first-line therapy had sustained DS (progression-free survival, 12, 17, and 22 months). The safety profile was consistent with that previously reported, with adverse events occurring in 9 patients (66.7%). Conclusions: This study suggests that everolimus is active in pNECG3with well-moderately differentiated morphology andKi67 less than 55%, inwhich more toxic systemic chemotherapy is, to date, the only available treatment.

Everolimus in pancreatic neuroendocrine carcinomas G3 / Panzuto, Francesco; Rinzivillo, Maria; Spada, Francesca; Antonuzzo, Lorenzo; Ibrahim, Toni; Campana, Davide; Fazio, Nicola; Delle Fave, Gianfranco. - In: PANCREAS. - ISSN 0885-3177. - STAMPA. - 46:3(2017), pp. 302-305. [10.1097/MPA.0000000000000762]

Everolimus in pancreatic neuroendocrine carcinomas G3

CAMPANA, DAVIDE;
2017

Abstract

Objective: The aim of this study was to investigate everolimus efficacy in well-moderately differentiated pancreatic NEC (pNEC) G3. Methods: This was a retrospective analysis of patients with pNEC G3 and Ki67 20% to 55% treated with everolimus. Results: Fifteen patients with median Ki67 30%and Eastern Cooperative Oncology Group performance status 0 to 1 were evaluated. Of these, 4 patients received everolimus as first-line treatment, whereas 11 had been pretreated with chemotherapy or peptide receptor radionuclide therapy. Median progression-free survival was 6 months, and median overall survival was 28 months. Eleven patients achieved disease stabilization (DS) at 3 month follow-up. Six patients (40%) maintained DS for at least 12 months. Three of 4 patients who received everolimus as first-line therapy had sustained DS (progression-free survival, 12, 17, and 22 months). The safety profile was consistent with that previously reported, with adverse events occurring in 9 patients (66.7%). Conclusions: This study suggests that everolimus is active in pNECG3with well-moderately differentiated morphology andKi67 less than 55%, inwhich more toxic systemic chemotherapy is, to date, the only available treatment.
2017
Everolimus in pancreatic neuroendocrine carcinomas G3 / Panzuto, Francesco; Rinzivillo, Maria; Spada, Francesca; Antonuzzo, Lorenzo; Ibrahim, Toni; Campana, Davide; Fazio, Nicola; Delle Fave, Gianfranco. - In: PANCREAS. - ISSN 0885-3177. - STAMPA. - 46:3(2017), pp. 302-305. [10.1097/MPA.0000000000000762]
Panzuto, Francesco; Rinzivillo, Maria; Spada, Francesca; Antonuzzo, Lorenzo; Ibrahim, Toni; Campana, Davide; Fazio, Nicola; Delle Fave, Gianfranco
File in questo prodotto:
Eventuali allegati, non sono esposti

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/580553
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 13
  • Scopus 56
  • ???jsp.display-item.citation.isi??? 48
social impact