Chen Chuangzhen, Chen Jianzhou, Luo Ting, Wang Siyan, Guo Hong, Zeng Chengbing, Wu Yanxuan, Liu Weitong, Huang Ruihong, Zhai Tiantian, Chen Zhijian, Li Derui
Department of Radiation Oncology, Cancer Hospital of Shantou University Medical College, Shantou, China.
Oncological Research Lab, Cancer Hospital of Shantou University Medical College, Shantou, China.
Front Oncol. 2021 Nov 18;11:738936. doi: 10.3389/fonc.2021.738936. eCollection 2021.
We aimed to evaluate the long-term outcomes of concurrent chemoradiotherapy (CCRT) with a simultaneous integrated boost (SIB) of radiotherapy for esophageal squamous cell carcinoma (ESCC).
Eighty-seven patients with primary ESCC enrolled in this phase II trial. The majority (92.0%) had locoregionally advanced disease. They underwent definitive chemoradiotherapy. The radiotherapy doses were 66 Gy for the gross tumor and 54 Gy for the subclinical disease. Doses were simultaneously administered in 30 fractions over 6 weeks. The patients also underwent concurrent and adjuvant chemotherapy, which comprised cisplatin and fluorouracil. The study end points were acute and late toxicities, first site of failure, locoregional tumor control, and overall survival rates.
The median follow-up time was 65.7 (range, 2.2-97.5) months for all patients and 81.5 (range, 19.4-97.5) months for those alive. There were 17 cases (19.5%) of severe late toxicities, including four cases (4.6%) of grade 5 and seven (8.0%) of grade 3 esophageal ulceration, four (4.6%) of grade 3 esophageal stricture, and two (2.3%) of grade 3 radiation-induced pneumonia. Twenty-three (26.4%) patients had locoregional disease progression. Most (86.7%) locally progressive lesions were within the dose-escalation region in the initial radiation plan, while majority of the recurrent lymph nodes were found out-of-field (83.3%) and in the supraclavicular region (75.0%). The 1-, 2-, 3-, and 5-year locoregional tumor control and overall survival rates were 79.2%, 72.4%, 72.4%, 70.8%, and 82.8%, 66.6%, 61.9%, 58.4%, respectively. Incomplete tumor response, which was assessed immediately after CCRT was an independent risk predictor of disease progression and death in ESCC patients.
CCRT with SIB was well tolerated in ESCC patients during treatment and long-term follow-up. Moreover, patients who underwent CCRT with SIB exhibited improved local tumor control and had better survival outcomes compared to historical data of those who had standard-dose radiotherapy.
我们旨在评估同步放化疗(CCRT)联合放疗同步整合加量(SIB)治疗食管鳞状细胞癌(ESCC)的长期疗效。
87例原发性ESCC患者纳入了这项II期试验。大多数患者(92.0%)患有局部区域晚期疾病。他们接受了根治性放化疗。放疗剂量为大体肿瘤66 Gy,亚临床病灶54 Gy。剂量在6周内分30次同步给予。患者还接受了同步和辅助化疗,包括顺铂和氟尿嘧啶。研究终点为急性和晚期毒性、首次失败部位、局部区域肿瘤控制和总生存率。
所有患者的中位随访时间为65.7(范围2.2 - 97.5)个月,存活患者为81.5(范围19.4 - 97.5)个月。有17例(19.5%)出现严重晚期毒性,包括4例(4.6%)5级和7例(8.0%)3级食管溃疡、4例(4.6%)3级食管狭窄和2例(2.3%)3级放射性肺炎。23例(26.4%)患者出现局部区域疾病进展。大多数(86.7%)局部进展性病变位于初始放疗计划的剂量递增区域内,而大多数复发淋巴结位于野外(83.3%)且在锁骨上区域(75.0%)。1年、2年、3年和5年的局部区域肿瘤控制率和总生存率分别为79.2%、72.4%、72.4%、70.8%和82.8%、66.6%、61.9%、58.4%。CCRT后立即评估的肿瘤反应不完全是ESCC患者疾病进展和死亡的独立风险预测因素。
ESCC患者在治疗和长期随访期间对CCRT联合SIB耐受性良好。此外,与接受标准剂量放疗患者的历史数据相比,接受CCRT联合SIB的患者局部肿瘤控制得到改善,生存结果更好。