Yang Xu, Zhai Yirui, Bi Nan, Zhang Tao, Deng Lei, Wang Wenqing, Wang Xin, Chen Dongfu, Zhou Zongmei, Wang Luhua, Liang Jun
Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100121, China.
Chin J Cancer Res. 2021 Feb 28;33(1):53-60. doi: 10.21147/j.issn.1000-9604.2021.01.06.
To investigate the safety and efficacy of nimotuzumab combined with radiotherapy for elderly patients with non-resectable esophageal carcinoma (EC).
Eligible patients were aged 70 years or older and had treatment-naïve, histologically proven inoperable locally advanced EC. Enrolled patients received radiotherapy with a total dose of 50-60 Gy in 25-30 fractions, concurrent with weekly infusion of nimotuzumab. The primary end point was the rate of more than grade 3 toxicities.
From June 2011 to July 2016, 46 patients with stage II-IV EC with a median age of 76.5 years were enrolled. There were 10, 28 and 8 patients with stage II, III and IV disease, respectively. The common acute toxicities included esophagitis (grade 1-2, 75.4%; grade 3, 8.7%), pneumonitis (grade 1, 4.3%; grade 2, 6.5%; grade 3, 2.2%), leukopenia (grade 1-2, 60.9%; grade 3-4, 4.4%), gastrointestinal reaction (grade 1-2, 17.3%; grade 3, 2.2%), thrombocytopenia (grade 1-2, 21.7%; grade 3, 2.2%), and radiothermitis (grade 1-2, 39.2%). The incidence of grade 3-4 adverse effects was 17.4%. No grade 5 toxicities were observed. Clinical complete response, partial response, stable disease, and progressive disease were observed in 1 (2.2%), 31 (67.4%), 12 (26.1%), and 2 (4.3%) patients, respectively. The median overall survival (OS) and progression-free survival (PFS) were 17 and 10 months, respectively. The 2-, 3-, and 5-year OS and PFS rates were 30.4%, 21.7%, 19.6%, and 26.1%, 19.6%, 19.6%, respectively.
Nimotuzumab combined with radiotherapy is a safe and effective therapy for elderly patients who are not surgical candidates. Further studies are warranted to confirm its therapeutic effects in elderly EC patients.
探讨尼妥珠单抗联合放疗治疗老年不可切除食管癌(EC)患者的安全性和有效性。
符合条件的患者年龄在70岁及以上,为未经治疗、经组织学证实无法手术的局部晚期EC患者。入组患者接受总剂量为50 - 60 Gy、分25 - 30次的放疗,同时每周输注尼妥珠单抗。主要终点是3级以上毒性反应发生率。
2011年6月至2016年7月,46例II - IV期EC患者入组,中位年龄76.5岁。其中II期、III期和IV期疾病患者分别有10例、28例和8例。常见的急性毒性反应包括食管炎(1 - 2级,75.4%;3级,8.7%)、肺炎(1级,4.3%;2级,6.5%;3级,2.2%)、白细胞减少(1 - 2级,60.9%;3 - 4级,4.4%)、胃肠道反应(1 - 2级,17.3%;3级,2.2%)、血小板减少(1 - 2级,21.7%;3级,2.2%)和放射性皮炎(1 - 2级,39.2%)。3 - 4级不良反应发生率为17.4%。未观察到5级毒性反应。临床完全缓解、部分缓解、病情稳定和疾病进展的患者分别有1例(2.2%)、31例(67.4%)、12例(26.1%)和2例(4.3%)。中位总生存期(OS)和无进展生存期(PFS)分别为17个月和10个月。2年、3年和5年的OS率分别为30.4%、21.7%、19.6%,PFS率分别为26.1%、19.6%、19.6%。
尼妥珠单抗联合放疗对于不适合手术的老年患者是一种安全有效的治疗方法。有必要进一步研究以证实其在老年EC患者中的治疗效果。