Neoadjuvant chemotherapy plus concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in elderly patients with stage III-IVa nasopharyngeal carcinoma: A real-world study based on medical comorbidities

被引:0
|
作者
Jin, Ya-Nan [1 ,2 ]
Xiao, Zhi-Wen [3 ]
Yao, Wei [2 ]
Yu, Jing [2 ]
Zhang, Wang-Jian [4 ]
Marks, Tia [5 ]
Zhang, Hong-Yu [2 ]
Yao, Ji-Jin [2 ]
Xia, Liang-Ping [1 ]
机构
[1] Sun Yat Sen Univ, State Key Lab Oncol South China, Guangdong Key Lab Nasopharyngeal Carcinoma Diag &, VIP Reg,Canc Ctr, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 5, Canc Ctr, Zhuhai, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Otolaryngol Head & Neck Surg, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Sch Publ Hlth, Dept Med Stat, Guangzhou, Guangdong, Peoples R China
[5] SUNY Albany, Sch Publ Hlth, Dept Environm Hlth Sci, Rensselaer, NY USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
concurrent chemoradiotherapy; elderly; nasopharyngeal carcinoma; neoadjuvant chemotherapy; risk stratification; SURVIVAL OUTCOMES; PROGNOSTIC MODEL; RADIOTHERAPY; IMPACT;
D O I
10.1002/hed.27689
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Purpose: To evaluate the outcomes and toxicities of adding neoadjuvant chemotherapy (NAC) to concurrent chemoradiotherapy (CCRT) in elderly (>= 65 years) patients with locoregionally advanced nasopharyngeal carcinoma (LANPC, stage III-IVa). Methods and Materials: Using an NPC-specific database, 245 elderly patients with stage III-IVa NPC, receiving CCRT +/- NAC, and an Adult Co-morbidity Evaluation 27 (ACE-27) score <2 were included. Recursive partitioning analysis (RPA) based on TNM stage and Epstein-Barr virus (EBV) DNA were applied for risk stratification. The primary end point was disease-free survival (DFS). Results: Two risk groups were generated by the RPA model. In the high-risk group (EBV DNA < 4000 copy/ml with stage IVa & EBV DNA >= 4000 copy/ml with stage III-IVa), patients treated with NAC plus CCRT achieved improved 5-year DFS rates compared to those who received CCRT alone (56.9% vs. 29.4%; p = 0.003). But we failed to observe the survival benefit of additional NAC in the low-risk group (EBV DNA <4000 copy/ml with stage III). The most common severe acute toxic effects were leucopenia (46.8% vs. 24.4%) and neutropenia (43.7% vs. 20.2%) in the NAC plus CCRT group versus CCRT group with statistically significant differences. Conclusions: The addition of NAC to CCRT was associated with better DFS for the high-risk group of elderly LANPC patients with ACE-27 score <2. However, the survival benefit of additional NAC was not observed in low-risk patients.
引用
收藏
页码:2020 / 2030
页数:11
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