Yao Bin, Tan Bingxu, Wang Cong, Song Qingxu, Wang Jianbo, Guan Shanghai, Jia Yibin, Ma Yanan, Huang Xiaochen, Sun Yi, Cheng Yufeng
Department of Radiation Oncology, Qilu Hospital, Shandong University, Jinan, People's Republic of China.
Ann Surg Oncol. 2016 Jul;23(7):2367-72. doi: 10.1245/s10434-016-5154-y. Epub 2016 Mar 1.
This retrospective study was designed to estimate the efficacy and toxicity of definitive radiotherapy with concurrent or sequential docetaxel/S-1 for patients with locally advanced esophageal squamous cell carcinoma (ESCC).
Of the 62 eligible patients enrolled in this study during January 1, 2010 to December 31, 2014 from Qilu Hospital, Shandong University, Shandong Province, 39 patients received 3 cycles of docetaxel/S-1 during and after radiotherapy (concurrent chemoradiotherapy, CCRT), and 23 patients had radiotherapy followed by 3 cycles of docetaxel and S-1 (sequential chemoradiotherapy, SCRT).
The CR of CCRT and SCRT groups were 48.72 and 21.74 %, respectively (p = 0.035). The median progress-free survival (PFS) of CCRT group (23.5 months) was significantly higher than SCRT group (11.7 months; p = 0.004). The median overall survival (OS) of CCRT group (33.5 months) also was significantly higher than SCRT group (24.0 months; p = 0.004). At 2 years, in this patient population, the rate of PFS of CCRT group was (44.2 ± 8.2 %), significantly higher than SCRT group (11.9 ± 9.6 %; p = 0.002). The 2-year OS rate of CCRT (68.6 ± 7.5 %) was significantly higher than SCRT group as well (42.0 ± 14.0 %; p = 0.002). The incidence of adverse events was higher in CCRT than SCRT group. No grade 4 or grade 5 adverse events occurred in our study.
Definitive radiotherapy with concurrent or sequential docetaxel and S-1 for inoperable locally advanced ESCC was very well tolerated and remarkably active. In both CCRT and SCRT groups, acute toxicities were manageable. This regimen holds promises for treatment of esophageal carcinoma and warrants further investigation.
本回顾性研究旨在评估多西他赛/S-1同步或序贯应用于局部晚期食管鳞状细胞癌(ESCC)患者根治性放疗中的疗效和毒性。
2010年1月1日至2014年12月31日期间,山东大学齐鲁医院纳入本研究的62例符合条件的患者中,39例患者在放疗期间及放疗后接受3个周期的多西他赛/S-1(同步放化疗,CCRT),23例患者先接受放疗,随后接受3个周期的多西他赛和S-1(序贯放化疗,SCRT)。
CCRT组和SCRT组的完全缓解(CR)率分别为48.72%和21.74%(p = 0.035)。CCRT组的中位无进展生存期(PFS)(23.5个月)显著高于SCRT组(11.7个月;p = 0.004)。CCRT组的中位总生存期(OS)(33.5个月)也显著高于SCRT组(24.0个月;p = 0.004)。在2年时,在该患者群体中,CCRT组的PFS率为(44.2±8.2%),显著高于SCRT组(11.9±9.6%;p = 0.002)。CCRT组的2年总生存率(68.6±7.5%)也显著高于SCRT组(42.0±14.0%;p = 0.002)。CCRT组不良事件的发生率高于SCRT组。本研究中未发生4级或5级不良事件。
多西他赛和S-1同步或序贯应用于无法手术的局部晚期ESCC的根治性放疗耐受性良好且活性显著。在CCRT组和SCRT组中,急性毒性均可控制。该方案有望用于食管癌的治疗,值得进一步研究。