0 226

Cited 10 times in

A Phase II Study of Nivolumab plus Gemcitabine in Patients with Recurrent or Metastatic Nasopharyngeal Carcinoma (KCSG HN17-11)

Authors
 Hyun Ae Jung  ;  Keon-Uk Park  ;  Sanghee Cho  ;  Jinyeong Lim  ;  Keun-Wook Lee  ;  Min Hee Hong  ;  Tak Yun  ;  Ho Jung An  ;  Woong-Yang Park  ;  Sergio Pereira  ;  Chan-Young Ock  ;  Bhumsuk Keam 
Citation
 CLINICAL CANCER RESEARCH, Vol.28(19) : 4240-4247, 2022-10 
Journal Title
CLINICAL CANCER RESEARCH
ISSN
 1078-0432 
Issue Date
2022-10
MeSH
Antineoplastic Combined Chemotherapy Protocols / adverse effects ; Artificial Intelligence ; B7-H1 Antigen / analysis ; B7-H1 Antigen / genetics ; Chromatin ; Deoxycytidine / analogs & derivatives ; Gemcitabine ; Humans ; Immune Checkpoint Inhibitors ; Nasopharyngeal Carcinoma / drug therapy ; Nasopharyngeal Carcinoma / etiology ; Nasopharyngeal Neoplasms* / drug therapy ; Nasopharyngeal Neoplasms* / genetics ; Nivolumab* / therapeutic use ; Programmed Cell Death 1 Receptor / therapeutic use
Abstract
Purpose: Although programmed death 1/programmed death ligand 1 (PD-1/PD-L1) inhibitors are promising agents for recurrent or metastatic nasopharyngeal carcinoma (NPC), PD-1/PD-L1 inhibitor monotherapy has shown modest efficacy. This study evaluated the efficacy and safety of nivolumab plus gemcitabine in patients with NPC who failed prior platinum-based chemotherapy.

Patients and methods: This is a phase II, multicenter, open-label, single-arm study. Patients with recurrent or metastatic NPC received nivolumab 3 mg/kg and gemcitabine 1,250 mg/m2 every 2 weeks until disease progression or intolerable toxicity. The primary endpoint was progression-free survival (PFS). The secondary endpoints included objective response rate (ORR), overall survival (OS), and safety. To identify potential biomarkers, whole-exome sequencing, whole-transcriptome sequencing, and immune phenotype analysis based on Lunit SCOPE IO, an artificial intelligence-powered spatial tumor-infiltrating lymphocyte analyzer, were performed.

Results: Thirty-six patients were enrolled between June 2018 and June 2019. The ORR was 36.1% and disease control rate was 97.2%. With median follow-up of 22.0 months, median PFS was 13.8 months [95% confidence interval (CI), 8.6-16.8 months]. Median OS was not reached, and OS rate at 6 months was 97.0% (95% CI, 80.4%-99.6%). The grade ≥3 treatment-related adverse events were hypertension (2.8%) and anemia (2.8%). In multivariate analysis of mutation of chromatin modifier gene, tumor mutational burden (≥ 2.1 mut/Mb), and somatic copy-number alteration (SCNA) level, the group with high SCNA (> 3 points; HR, 7.0; 95% CI, 1.3-37.9; P = 0.02) had independently associated with poor PFS. Immune phenotype analysis showed that tumors with high proportion of immune-excluded immune phenotype was significantly correlated with poor PFS (HR, 4.4; 95% CI, 1.2-16.2; P = 0.018).

Conclusions: Nivolumab plus gemcitabine showed promising efficacy with favorable toxicity profiles in patients with advanced NPC in whom platinum-based combination chemotherapy failed.
Full Text
https://aacrjournals.org/clincancerres/article/28/19/4240/709307/A-Phase-II-Study-of-Nivolumab-plus-Gemcitabine-in
DOI
10.1158/1078-0432.CCR-22-1238
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Hong, Min Hee(홍민희) ORCID logo https://orcid.org/0000-0003-3490-2195
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/193358
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links