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同步放化疗联合尼妥珠单抗治疗局部晚期鼻咽癌患者的近期疗效和毒副反应分析

徐洪波 张亚军 黄志飞 赵红雨 刘子璇 高波 蔡丰 宋世龙 何泽来 江浩

徐洪波, 张亚军, 黄志飞, 赵红雨, 刘子璇, 高波, 蔡丰, 宋世龙, 何泽来, 江浩. 同步放化疗联合尼妥珠单抗治疗局部晚期鼻咽癌患者的近期疗效和毒副反应分析[J]. 中华全科医学, 2024, 22(2): 206-208. doi: 10.16766/j.cnki.issn.1674-4152.003366
引用本文: 徐洪波, 张亚军, 黄志飞, 赵红雨, 刘子璇, 高波, 蔡丰, 宋世龙, 何泽来, 江浩. 同步放化疗联合尼妥珠单抗治疗局部晚期鼻咽癌患者的近期疗效和毒副反应分析[J]. 中华全科医学, 2024, 22(2): 206-208. doi: 10.16766/j.cnki.issn.1674-4152.003366
XU Hongbo, ZHANG Yajun, HUANG Zhifei, ZHAO Hongyu, LIU Zixuan, GAO Bo, CAI Feng, SONG Shilong, HE Zelai, JIANG Hao. Analysis of the short-term efficacy and side effects of concurrent chemoradiotherapy combined with nimotuzumab in patients with locally advanced nasopharyngeal carcinoma[J]. Chinese Journal of General Practice, 2024, 22(2): 206-208. doi: 10.16766/j.cnki.issn.1674-4152.003366
Citation: XU Hongbo, ZHANG Yajun, HUANG Zhifei, ZHAO Hongyu, LIU Zixuan, GAO Bo, CAI Feng, SONG Shilong, HE Zelai, JIANG Hao. Analysis of the short-term efficacy and side effects of concurrent chemoradiotherapy combined with nimotuzumab in patients with locally advanced nasopharyngeal carcinoma[J]. Chinese Journal of General Practice, 2024, 22(2): 206-208. doi: 10.16766/j.cnki.issn.1674-4152.003366

同步放化疗联合尼妥珠单抗治疗局部晚期鼻咽癌患者的近期疗效和毒副反应分析

doi: 10.16766/j.cnki.issn.1674-4152.003366
基金项目: 

安徽省中央引导地方科技发展资金项目 2020b07030008

安徽省高校自然科学研究项目 KJ2021A0781

详细信息
    通讯作者:

    江浩,E-mail: jianghao1223@163.com

  • 中图分类号: R739.6 R730.58

Analysis of the short-term efficacy and side effects of concurrent chemoradiotherapy combined with nimotuzumab in patients with locally advanced nasopharyngeal carcinoma

  • 摘要:   目的  鼻咽癌具有独特的解剖学和生物学特性,放疗或同步放化疗是一种有效的治疗模式,然而,仍有许多局部晚期鼻咽癌患者出现局部复发或远处转移,因此,靶向治疗为鼻咽癌患者提供了更多的选择。本研究旨在评估同步放化疗联合尼妥珠单抗在治疗局部晚期鼻咽癌患者中的近期疗效和毒副反应,并进一步分析调强放射治疗(IMRT)和螺旋断层放射治疗(TOMO)对患者副反应的影响。  方法  回顾性分析2020年12月—2023年6月蚌埠医科大学第一附属医院放疗科收治的88例局部晚期鼻咽癌患者的临床资料,治疗组44例患者接受同步放化疗联合尼妥珠单抗靶向治疗,对照组44例患者仅接受同步放化疗,对比分析2组的近期疗效和毒副反应发生情况以及不同放疗方法对副反应的影响。  结果  治疗组患者鼻咽部和颈部淋巴结的总有效率(ORR)分别为97.8%(43/44)和93.2%(41/44),对照组的ORR分别为81.8%(36/44)和81.8%(36/44)。治疗组的黏膜炎发生率高于对照组[84.1%(37/44)vs. 63.6%(28/44), P<0.05]。进一步分析显示治疗组和对照组中接受TOMO放疗的患者黏膜炎发生率均低于IMRT,但差异无统计学意义(P>0.05)。  结论  对于局部晚期的鼻咽癌患者,同步放疗化疗联合尼妥珠单抗近期疗效更好,采用TOMO放疗的患者黏膜反应有降低趋势。

     

  • 表  1  2组局部晚期鼻咽癌患者一般临床资料比较(例)

    Table  1.   Comparison of general clinical data between the two groups of patients with locally advanced nasopharyngeal carcinoma (cases)

    组别 例数 性别 年龄(岁) KPS(分) T N 放疗技术
    男性 女性 ≥60 <60 ≥90 <90 1~2 3~4 0~1 2~3 IMRT TOMO
    治疗组 44 36 8 10 34 31 13 13 31 21 23 29 15
    对照组 44 30 14 8 36 27 17 17 27 19 25 14 30
    χ2 2.182 2.279 0.809 0.809 0.183 10.233
    P 0.140 0.597 0.368 0.368 0.669 0.001
    下载: 导出CSV

    表  2  2组局部晚期鼻咽癌患者近期疗效比较[例(%)]

    Table  2.   Comparison of short-term efficacy between the two groups of patients with locally advanced nasopharyngeal carcinoma [cases (%)]

    组别 例数 完全缓解 部分缓解 稳定 进展 ORR
    鼻咽部治疗组 44 20(45.5) 23(52.3) 1(2.2) 0 43(97.8)
    鼻咽部对照组 44 12 (27.3) 24(54.5) 8(18.2) 0 36(81.8)
    χ2 4.456
    P 0.035
    组别 例数 完全缓解 部分缓解 稳定 进展 ORR
    颈部治疗组 44 13 (29.5) 28(63.7) 3(6.8) 0 41(93.2)
    颈部对照组 44 17 (38.6) 19(43.2) 8(18.2) 0 36(81.8)
    χ2 2.597
    P 0.107
    下载: 导出CSV

    表  3  2组局部晚期鼻咽癌患者急性副反应发生情况比较(例)

    Table  3.   Comparison of acute side effects between the two groups of patients with locally advanced nasopharyngeal carcinoma (cases)

    组别 反应级别 血液类 非血液类
    白细胞减少 中性粒减少 贫血 血小板减少 急性胃肠道反应 疲乏 肝肾功能受损 口腔黏膜炎症 放射性皮炎
    治疗组 0级 12 19 23 28 8 40 39 7 19
    1~2级 22 17 20 14 32 4 5 17 18
    3~4级 10 8 1 2 4 0 0 20 7
    对照组 0级 19 29 26 23 9 40 37 16 21
    1~2级 17 11 18 17 30 4 7 14 19
    3~4级 8 4 0 4 5 0 0 14 4
    χ2 2.440 4.583 0.414 1.166 0.073 0.000 0.386 4.768 0.183
    P 0.118 0.320 0.520 0.280 0.787 1.000 0.534 0.029 0.669
    下载: 导出CSV

    表  4  2组局部晚期鼻咽癌患者口腔黏膜炎发生情况比较(例)

    Table  4.   Comparison of the incidence of oral mucositis between the two groups of patients with locally advanced nasopharyngeal carcinoma (cases)

    组别 治疗组 对照组
    阳性 阴性 阳性 阴性
    IMRT 27 2 10 4
    TOMO 10 5 18 12
    χ2 3.378 0.539
    P 0.066 0.463
    下载: 导出CSV
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  • 收稿日期:  2023-09-11
  • 网络出版日期:  2024-03-27

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