Wang Run-Jie, Ke Rui-Quan, Yu Yi-Feng, Lu Guan-Zhong, Wu San-Gang
Department of Radiation Oncology, Xiamen Cancer Quality Control Center, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Front Pharmacol. 2024 Mar 21;15:1366853. doi: 10.3389/fphar.2024.1366853. eCollection 2024.
To investigate the survival outcomes and toxicities associated with the addition of nimotuzumab to concurrent chemoradiotherapy (CCRT) in locally advanced nasopharyngeal carcinoma (LANPC) patients who received induction chemotherapy (IC).
Patients with stage III-IVA nasopharyngeal carcinoma who received IC and CCRT between January 2017 and October 2021 were retrospectively included. We aimed to compare the locoregional recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) between patients treated with CCRT+nimotuzumab and CCRT alone.
We included 411 patients in the analysis. Of these patients, 267 (65.0%) and 144 (35.0%) had CCRT+nimotuzumab and CCRT alone, respectively. Similar LRFS was found between those with and without nimotuzumab (92.9% vs. 92.6%, = 0.855). The 3-year DMFS was 88.2% and 76.2% in those with and without nimotuzumab ( = 0.002). The 3-year DFS was 83.4% and 70.6% in those with and without nimotuzumab treatment ( = 0.003). The 3-year OS was 92.1% and 81.1% in those with and without nimotuzumab ( = 0.003). The multivariate Cox regression analysis indicated that the addition of nimotuzumab was independently associated with better DMFS (hazard ratio [HR] 0.606, = 0.049), DFS (HR 0.613, = 0.028), and OS (HR 0.497, = 0.019). No significant differences in major toxicities were found between the two treatment arms, including hematologic toxicities, hepatoxicity, nephrotoxicity, gastrointestinal reactions, and mucositis (all > 0.05).
The addition of nimotuzumab to CCRT after IC in LANPC has shown promising results in improving treatment outcomes and acceptable toxicities.
探讨在接受诱导化疗(IC)的局部晚期鼻咽癌(LANPC)患者中,同步放化疗(CCRT)联合尼妥珠单抗的生存结局和毒性反应。
回顾性纳入2017年1月至2021年10月期间接受IC和CCRT的III-IVA期鼻咽癌患者。我们旨在比较CCRT联合尼妥珠单抗治疗的患者与单纯CCRT治疗的患者之间的局部区域无复发生存期(LRFS)、远处转移无复发生存期(DMFS)、无病生存期(DFS)和总生存期(OS)。
我们纳入了411例患者进行分析。其中,267例(65.0%)接受CCRT联合尼妥珠单抗治疗,144例(35.0%)接受单纯CCRT治疗。使用和未使用尼妥珠单抗的患者之间LRFS相似(92.9%对92.6%,P = 0.855)。使用和未使用尼妥珠单抗的患者3年DMFS分别为88.2%和76.2%(P = 0.002)。使用和未使用尼妥珠单抗治疗的患者3年DFS分别为83.4%和70.6%(P = 0.003)。使用和未使用尼妥珠单抗的患者3年OS分别为92.1%和81.1%(P = 0.003)。多因素Cox回归分析表明,添加尼妥珠单抗与更好的DMFS(风险比[HR]0.606,P = 0.049)、DFS(HR 0.613,P = 0.028)和OS(HR 0.497,P = 0.019)独立相关。在两个治疗组之间未发现主要毒性反应的显著差异,包括血液学毒性、肝毒性、肾毒性、胃肠道反应和粘膜炎(均P>0.05)。
在LANPC患者IC后CCRT中添加尼妥珠单抗在改善治疗结局和可接受的毒性方面显示出有前景的结果。