Tislelizumab plus neoadjuvant chemotherapy and concurrent chemoradiotherapy versus neoadjuvant chemotherapy and concurrent chemoradiotherapy for locally advanced nasopharyngeal carcinoma: A retrospective study

被引:1
|
作者
He, Jiaqi [1 ]
Luo, Guoqing [2 ]
Liu, Shen [1 ]
Chen, Lingli [3 ]
Chen, Zihong [1 ]
Zhang, Bing [4 ]
Lin, Jiong [1 ]
Qin, Wenyi [5 ]
Li, Haiwen [1 ]
Zhou, Haideng [1 ]
Yu, Ying [1 ]
Zhan, Dechao [1 ]
Yang, Donghong [1 ]
Luo, Haiqing [1 ]
机构
[1] Guangdong Med Univ, Affiliated Hosp, Specialty Head & Neck Oncol, Zhanjiang 524001, Peoples R China
[2] Guangdong Med Univ, Affiliated Hosp, Otorhinolaryngol Dept, Zhanjiang 524001, Peoples R China
[3] Guangdong Med Univ, Clin Med Coll 1, Zhanjiang 524023, Peoples R China
[4] Guangdong Med Univ, Affiliated Hosp, Plast Surg Dept, Zhanjiang 524001, Peoples R China
[5] Guangdong Med Univ, Affiliated Hosp, Thyroid & Breast Surg Dept, Zhanjiang 524001, Peoples R China
来源
TRANSLATIONAL ONCOLOGY | 2024年 / 48卷
关键词
Locally advanced nasopharyngeal carcinoma; Tislelizumab; Immunotherapy; Nano albumin-paclitaxel; ANTITUMOR-ACTIVITY; NAB-PACLITAXEL; MULTICENTER; CISPLATIN; PHASE-3; TRIAL;
D O I
10.1016/j.tranon.2024.102058
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The efficacy of immunotherapy plus neoadjuvant chemotherapy and concurrent chemoradiotherapy (CCRT) for locally advanced nasopharyngeal carcinoma (LA-NPC) has not been reported. This study retrospectively compared the efficacy of tislelizumab plus neoadjuvant chemotherapy and CCRT with neoadjuvant chemotherapy followed by CCRT. Methods: Ninety patients with stages III-IVa NPC were identified between January 2020 and March 2021 at the Affiliate Hospital of Guangdong Medical University. Forty-three patients in the observation group (OG) received tislelizumab plus nano albumin-paclitaxel and cisplatin (nab-TP) regimen, followed by CCRT, while forty-seven patients in the control group (CG) received nab-TP regimen followed by CCRT. Results: The complete response rate after neoadjuvant therapy was significantly higher in the OG compared to the CG (37.2% vs. 12.8 %). The objective response rates were 88.4 % in the OG and 70.2 % in the CG. The 3-year progression-free survival (PFS) rates for OG and CG patients were 93.0 % and 78.7%, respectively (P = 0.04, HR = 0.31). The overall survival (OS) rates for the OG and the CG were 95.3 % and 87.2 %, respectively (P = 0.15, HR = 0.36). Locoregional relapse-free survival (LRFS) rates were 90.7 % for the OG and 72.3 % for the CG (P = 0.04, HR = 0.38), and distant metastasis-free survival (DMFS) rates were 95.3 % for the OG, and 80.9 % for the CG (P = 0.04, HR = 0.30). For PD-L1 high-expression and low-expression rates, the 3-year PFS rates were 89.2 % and 85.7% (P = 0.77, HR = 1.21), and the OS rates were 90.2% and 89.2% (P = 0.65, HR = 1.36), respectively. Conclusion: Tislelizumab combined with neoadjuvant chemotherapy and CCRT showed encouraging therapeutic effects and good tolerability in patients with LA-NPC compared to the standard treatment.
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