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抗表皮生长因子受体(EGFR)单克隆抗体联合放化疗用于诱导化疗耐药的局部晚期鼻咽癌:一项前瞻性II期研究。

Anti-epidermal growth factor receptor (EGFR) monoclonal antibody combined with chemoradiotherapy for induction chemotherapy resistant locally advanced nasopharyngeal carcinoma: A prospective phase II study.

作者信息

Niu Xiaoshuang, Liu Peiyao, Zhou Xin, Ou Dan, Wang Xiaoshen, Hu Chaosu

机构信息

Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China; Department of Radiation Oncology, Shanghai Clinical Research Center for Radiation Oncology, Shanghai, China; Shanghai Key Laboratory of Radiation Oncology, Shanghai, China.

Department of Radiation Oncology, Eye & ENT Hospital, Fudan University, Shanghai, China.

出版信息

Transl Oncol. 2024 Jan;39:101797. doi: 10.1016/j.tranon.2023.101797. Epub 2023 Oct 20.

Abstract

OBJECTIVES

To investigate the efficacy and safety of nimotuzumab (NTZ) combined with concurrent chemo-radiotherapy (CCRT) in induction chemotherapy (IC) resistant locally advanced nasopharyngeal carcinoma (LANPC).

MATERIALS AND METHODS

A single-arm, open-label phase II clinical trial was conducted (NCT04508816). Eligible patients were 18-70 years old, pathologically confirmed NPC at stage III-IVA, stable disease or progressive disease after IC by imaging evaluation, and ECOG performance status with 0-1. All patients received intensity-modulated radiotherapy (IMRT) concurrent with chemotherapy and NTZ (200 mg/w). The primary endpoint was progression-free survival (PFS). The secondary endpoints were overall survival (OS), objective response rate (ORR) and safety.

RESULTS

From May 2015 to July 2020, 56 NPC patients were enrolled. With the median follow-up of 34 months (range from 8 to 77 months), the 3-year and 5-year PFS and OS rates were 79.3 % and 72.1 %, 94.0 % and 87.2 %, respectively. ORR of the nasopharynx and cervical lymph nodes involvement were 98.2 % and 98.1 % three months after IMRT. Univariate analysis revealed that pretreatment PET/CT was the factor that influenced PFS (P = 0.038). Patients treated with ≥6 weeks of NTZ showed improved 3-year PFS rate (83.0% vs. 73.9 %, P > 0.05) and 5-year PFS rate (83.0% vs. 61.6 %, P>0.05) compared with <6 weeks NTZ. The acute toxicities were mainly grade 1/2 hematologic. Severe toxicities were uncommon. The major grade 3/4 AE was neutropenia (26.8 %).

CONCLUSIONS

The results demonstrated that NTZ combined with CCRT in IC resistant LANPC was effective with mild toxicity.

摘要

目的

探讨尼妥珠单抗(NTZ)联合同步放化疗(CCRT)用于诱导化疗(IC)耐药的局部晚期鼻咽癌(LANPC)的疗效和安全性。

材料与方法

开展一项单臂、开放标签的II期临床试验(NCT04508816)。符合条件的患者年龄在18至70岁之间,经病理确诊为III-IVA期鼻咽癌,经影像学评估在IC后疾病稳定或进展,且东部肿瘤协作组(ECOG)体能状态为0-1。所有患者均接受调强放疗(IMRT),同时进行化疗和NTZ(200mg/周)。主要终点为无进展生存期(PFS)。次要终点为总生存期(OS)、客观缓解率(ORR)和安全性。

结果

2015年5月至2020年7月,共纳入56例鼻咽癌患者。中位随访34个月(范围8至77个月),3年和5年PFS率分别为79.3%和72.1%,OS率分别为94.0%和87.2%。IMRT三个月后,鼻咽部和颈部淋巴结受累的ORR分别为98.2%和98.1%。单因素分析显示,治疗前PET/CT是影响PFS的因素(P = 0.038)。与接受NTZ治疗时间<6周的患者相比,接受NTZ治疗≥6周的患者3年PFS率(83.0%对73.9%,P>0.05)和5年PFS率(83.0%对61.6%,P>0.05)有所提高。急性毒性主要为1/2级血液学毒性。严重毒性不常见。主要的3/4级不良事件为中性粒细胞减少(26.8%)。

结论

结果表明,NTZ联合CCRT用于IC耐药的LANPC有效且毒性轻微。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c1/10597793/80e3fb7859e1/gr1.jpg

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