Induction chemotherapy plus chemoradiotherapy in esophageal cancer: long-term results and exploratory analyses of a randomized controlled trial

被引:0
|
作者
Liu, Shiliang [1 ,2 ]
Chen, Baoqing [1 ,2 ]
Zhu, Yujia [1 ,2 ]
Wang, Sifen [1 ,2 ]
Cheng, Xingyuan [1 ,2 ]
Wang, Ruixi [1 ,2 ]
Hu, Yonghong [1 ,2 ]
Liu, Hui [1 ,2 ]
Li, Qiaoqiao [1 ,2 ]
Zhang, Li [1 ,2 ]
Zhao, Lei [1 ,2 ]
Liu, Mengzhong [1 ,2 ]
Xi, Mian [1 ,2 ]
机构
[1] Guangdong Esophageal Canc Inst, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Canc Ctr, Dept Radiat Oncol, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
基金
中国国家自然科学基金;
关键词
Esophageal squamous cell carcinoma; induction chemotherapy; definitive chemoradiotherapy; response rate; survival; SQUAMOUS-CELL CARCINOMA; DEFINITIVE CHEMORADIOTHERAPY; CISPLATIN; CHEMORADIATION; ADENOCARCINOMA; FLUOROURACIL; SURGERY; THERAPY;
D O I
10.1093/oncolo/oyae295
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Previous results of our trial demonstrated that the addition of induction chemotherapy (IC) prior to defnitive chemoradiotherapy (CRT) failed to signifcantly improve the response rate or 3-year survival in patients with locally advanced esophageal squamous cell carcinoma (ESCC). Here, we report long-term results and exploratory analyses to further evaluate the therapeutic value of IC.<br /> Methods: Patients with previously untreated, unresectable, stage II-IVA ESCC were randomly assigned to receive IC followed by CRT or CRT alone. The relationship between tumor response to IC and long-term survival was analyzed. Baseline tumor biopsies were collected for RNA-Seq to identify patients who may beneft from IC.<br /> Results: Eligible patients were randomized to either the IC + CRT group (n = 55) or the CRT group (n = 55). With a median follow-up of 74.9 months, the 5-year overall survival rate was 31.8% in the IC + CRT group and 29.1% in the CRT group (P =.675; HR, 0.91; 95% CI, 0.58-1.43). Similarly, no signifcant differences were identifed in 5-year progression-free survival between groups (30.5% vs 25.5%, P =.508; HR, 0.86; 95% CI, 0.56-1.34). Patients who responded to IC had signifcantly better survival than nonresponders. A risk-score model incorporating 6 key genes to predict IC effcacy was also constructed.<br /> Conclusions: Compared with defnitive CRT alone, the addition of IC before CRT still failed to demonstrate superior survival in patients with unselected ESCC, based on long-term follow-up. However, because IC responders were associated with more favorable survival, potential molecular biomarkers were identifed for selection of beneft population from IC
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页数:9
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