Anti-programmed death-1 inhibitors and nimotuzumab in combination with induction chemotherapy for locoregionally advanced nasopharyngeal carcinoma: A propensity score-matched analysis.

C Chunyan Chen Y Ya-Ni Zhang (State Key Laboratory of Membrane Biology, IDG/McGovern Institute for Brain Research, School of Life Sciences, Tsinghua University) Y Yu-Pei Chen P Pu-Yun OuYang (Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China) T Tai-xiang Lu (Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China) F Fangyun Xie (Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, Guangdong, China) F Fei Han

Abstract

6060 Background: The poor prognosis of locoregionally advanced nasopharyngeal carcinoma (LANPC) due to the high incidence of metastasis necessitates effective treatment strategies. Synergistic effects have been observed when anti-programmed death-1 (anti-PD-1) inhibitors are combined with chemotherapy or targeted therapy. Methods: In total, 319 patients with LANPC were retrospectively enrolled between December 2017 and November 2022. The primary endpoint was progression-free survival. Propensity score matching was performed to adjust for potential confounders. Results: Overall, 150 patients were included after propensity score matching. The immunotherapy + nimotuzumab + chemotherapy (INC) group (n=50) had a higher 3-year progression-free survival rate (96.6% [95% confidence interval (CI): 93.2–100.0]) than the nimotuzumab + chemotherapy (NC) group (n=100) (79.8% [95% CI: 75.6–84.0]). The INC group had a hazard ratio of 0.16 (95% CI: 0.02–1.22; P=0.04). The objective response rates were 100% and 99% for the INC and NC groups, respectively. Grade ≥3 treatment-related adverse events were reported in eight (5.3%) patients, and hyponatremia (2.0%) was the most common. Grade ≥3 immune-related adverse events (rash and reactive capillary proliferation) were reported in two (4.0%) patients. Conclusions: Neoadjuvant therapy with anti-PD-1 inhibitors and nimotuzumab combined with chemotherapy demonstrates promising anti-tumor activity with acceptable safety for LANPC. More well-designed randomized trials with larger patient cohorts are needed to confirm long-term efficacy. Short-term efficacy of three months after the end of treatment. Response evaluation INC group [n = 50 (%)] NC group [n = 100 (%)] CR 38(76.0) 19(19.0) PR 12(24.0) 80(80.0) SD 0 1(1.0) PD 0 0 ORR (95% CI) 100% (92.9%, 100%) 99% (94.6%, 100%) DCR (95% CI) 100% (92.9%, 100%) 100% (96.4%, 100%) CI, confidence interval; CR, complete response; DCR, disease control rate; IC, induction chemotherapy; ORR, objective response rate; PD, progressive disease; PR, partial response; SD, stable disease.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 6060-6060
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (7)

C

Chunyan Chen

Y

Ya-Ni Zhang

State Key Laboratory of Membrane Biology, IDG/McGovern Institute for Brain Research, School of Life Sciences, Tsinghua University

Y

Yu-Pei Chen

P

Pu-Yun OuYang

Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China

T

Tai-xiang Lu

Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China

F

Fangyun Xie

Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, Guangdong, China

F

Fei Han