Nomogram-aided individual induction chemotherapy regimen selection in advanced nasopharyngeal carcinoma

被引:6
作者
Peng, Hao [1 ,2 ]
Chen, Lei [2 ]
Mao, Yan-Ping [2 ]
Tian, Li [3 ]
Liu, Li-Zhi [3 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Precis Med Inst, Ctr Translat Med, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Guangdong Key Lab Nasopharyngeal Carcinoma Diag &, State Key Lab Oncol Southern China,Canc Ctr, Collaborat Innovat Ctr Canc Med,Dept Radiat Oncol, Guangzhou 510060, Peoples R China
[3] Sun Yat Sen Univ, Imaging Diag & Intervent Ctr, State Key Lab Oncol Southern China, Collaborat Innovat Ctr Canc Med,Canc Ctr, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Nasopharyngeal carcinoma; Induction chemotherapy; Nomogram; Prognosis; COMPARING NEOADJUVANT CHEMOTHERAPY; PLUS CONCURRENT CHEMORADIOTHERAPY; INTENSITY-MODULATED RADIOTHERAPY; RANDOMIZED PHASE-II; ADJUVANT CHEMOTHERAPY; TRIAL; CISPLATIN; SURVIVAL; MULTICENTER; DOCETAXEL;
D O I
10.1016/j.oraloncology.2021.105555
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: We undertook this study to clarify how TPF, TP and PF induction chemotherapy (IC) regimens benefit for nasopharyngeal carcinoma (NPC) patients with different risk of disease progression. Materials and Methods: Patients with newly diagnosed, stage III-IVA NPC were included. A quantitative nomogram was built using the independent prognostic factors identified for disease-free survival (DFS). Patients were stratified into low-risk and high-risk groups by the nomogram. Survival outcomes and toxicities between different IC regimens were compared. Results: In total, 1647 (41.0%), 1123 (28.0%) and 1242 (31.0%) patients received TPF, PF and TP regimen, respectively. Consequently, 2253 (56.2%) patients were clarified as low-risk group and the other 1759 (43.8%) as high-risk group. Survival outcomes did not significantly differ between TPF, PF and TP regimens within the low-risk group. However, TPF was associated with significantly improved 3-year DFS (76.2% vs. 67.5% vs. 68.3%), overall survival (88.3% vs. 84.1% vs. 83.9%), distant metastasis-free survival (81.9% vs. 75.0% vs. 77.4%) and locoregional relapse-free survival (92.0% vs. 87.5% vs. 86.9%; all P < 0.05) compared with PF and TP within high-risk group. Multivariate analysis also confirmed these findings. Toxicity analysis showed that TP regimen has the highest percentage of grade 3-5 hematologic toxicities while PF regimen achieved the lowest percentages of overall grade 3-5 adverse events. Conclusions: Patients with high risk should receive TPF for better efficacy and PF may be a better choice for low risk patients with regard to less grade 3-5 toxicities.
引用
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页数:8
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