Back to Search Start Over

Data from Rb Loss and KRAS Mutation Are Predictors of the Response to Platinum-Based Chemotherapy in Pancreatic Neuroendocrine Neoplasm with Grade 3: A Japanese Multicenter Pancreatic NEN-G3 Study

Authors :
Nobumasa Mizuno
Yasushi Yatabe
Junji Furuse
Masayuki Imamura
Kazuo Hara
Tsukasa Yoshida
Nobutaka Matayoshi
Tadayuki Takagi
Katsuyuki Miyabe
Go Murohisa
Atsushi Kanno
Tetsuya Mine
Yoshiaki Kawaguchi
Syunpei Hashigo
Akihito Tsuji
Hiroki Tanaka
Izumi Komoto
Yoshiaki Tsuchiya
Hiroyuki Maguchi
Kei Yane
Masayuki Kitano
Hiroki Taguchi
Kenji Notohara
Hiroaki Yanagimoto
Takuji Okusaka
Chigusa Morizane
Yuzo Kodama
Hiroshi Ishii
Shoji Nakamori
Tetsuhide Ito
Masafumi Ikeda
Noritoshi Kobayashi
Hideyuki Yoshitomi
Masayuki Furukawa
Makoto Ueno
Keitaro Matsuo
Waki Hosoda
Susumu Hijioka
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

Abstract

Purpose: Patients with pancreatic neuroendocrine neoplasm grade-3 (PanNEN-G3) show variable responses to platinum-based chemotherapy. Recent studies indicated that PanNEN-G3 includes well-differentiated neuroendocrine tumor with G3 (NET-G3). Here, we examined the clinicopathologic and molecular features of PanNEN-G3 and assessed the responsiveness to chemotherapy and survival.Experimental Design: A total of 100 patients with PanNEN-G3 were collected from 31 institutions, and after central review characteristics of each histologic subtype [NET-G3 vs. pancreatic neuroendocrine carcinoma (NEC-G3)] were analyzed, including clinical, radiological, and molecular features. Factors that correlate with response to chemotherapy and survival were assessed.Results: Seventy patients analyzed included 21 NETs-G3 (30%) and 49 NECs-G3 (70%). NET-G3 showed lower Ki67-labeling index (LI; median 28.5%), no abnormal Rb expression (0%), and no mutated KRAS (0%), whereas NEC-G3 showed higher Ki67-LI (median 80.0%), Rb loss (54.5%), and KRAS mutations (48.7%). Chemotherapy response rate (RR), platinum-based chemotherapy RR, and prognosis differed significantly between NET-G3 and NEC-G3. Chemotherapeutic outcomes were worse in NET-G3 (P < 0.001). When we stratified PanNEN-G3 with Rb and KRAS, PanNENs-G3 with Rb loss and those with mutated KRAS showed significantly higher RRs to platinum-based chemotherapy than those without (Rb loss, 80% vs. normal Rb, 24%, P = 0.006; mutated KRAS, 77% versus wild type, 23%, P = 0.023). Rb was a predictive marker of response to platinum-based chemotherapy even in NEC-G3 (P = 0.035).Conclusions: NET-G3 and NEC-G3 showed distinct clinicopathologic characteristics. Notably, NET-G3 does not respond to platinum-based chemotherapy. Rb and KRAS are promising predictors of response to platinum-based chemotherapy for PanNEN-G3, and Rb for NEC-G3. Clin Cancer Res; 23(16); 4625–32. ©2017 AACR.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....1afbb5562d112f73eab764348ea0d12c