自拟健脾补肾和胃组方联合化疗对晚期脾肾虚弱型大肠癌患者的临床疗效及作用机制研究

何新颖, 高志远, 梁伟, 等. 自拟健脾补肾和胃组方联合化疗对晚期脾肾虚弱型大肠癌患者的临床疗效及作用机制研究[J]. 中国中西医结合消化杂志, 2024, 32(11): 1012-1016. doi: 10.3969/j.issn.1671-038X.2024.11.13
引用本文: 何新颖, 高志远, 梁伟, 等. 自拟健脾补肾和胃组方联合化疗对晚期脾肾虚弱型大肠癌患者的临床疗效及作用机制研究[J]. 中国中西医结合消化杂志, 2024, 32(11): 1012-1016. doi: 10.3969/j.issn.1671-038X.2024.11.13
HE Xinying, GAO Zhiyuan, LIANG Wei, et al. Study on clinical efficacy and mechanism of self-designed spleen-bushen and stomach formula with chemotherapy in advanced colorectal cancer patients with weak spleen and kidney deficiency[J]. Chin J Integr Tradit West Med Dig, 2024, 32(11): 1012-1016. doi: 10.3969/j.issn.1671-038X.2024.11.13
Citation: HE Xinying, GAO Zhiyuan, LIANG Wei, et al. Study on clinical efficacy and mechanism of self-designed spleen-bushen and stomach formula with chemotherapy in advanced colorectal cancer patients with weak spleen and kidney deficiency[J]. Chin J Integr Tradit West Med Dig, 2024, 32(11): 1012-1016. doi: 10.3969/j.issn.1671-038X.2024.11.13

自拟健脾补肾和胃组方联合化疗对晚期脾肾虚弱型大肠癌患者的临床疗效及作用机制研究

  • 基金项目:
    河北省自然科学基金项目(No:H2023110021)
详细信息

Study on clinical efficacy and mechanism of self-designed spleen-bushen and stomach formula with chemotherapy in advanced colorectal cancer patients with weak spleen and kidney deficiency

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  • 目的 观察自拟健脾补肾和胃组方联合化疗对晚期脾肾虚弱型大肠癌患者的临床疗效、中医证候及生活质量的影响。方法 将50例脾肾虚弱型大肠癌患者随机分为治疗组和对照组。对照组给予CAPEOX联合贝伐珠单抗方案化疗,治疗组在此基础上加服自拟健脾补肾和胃组方汤剂(每日1剂,连服8周),化疗每3周重复1次,连用3个周期后观察两组的临床疗效、中医证候评分、生活质量及Bcl-2、Bax的表达情况。结果 3周期治疗后,治疗组与对照组的临床总体疗效相当;中医证候积分和中医证候疗效比较,治疗组优于对照组(P < 0.05);治疗后,两组患者Bcl-2的表达均较治疗前下降(P < 0.01),Bax的表达均较治疗前升高(P < 0.01),且治疗组的变化比对照组更明显(P < 0.05)。结论 自拟健脾补肾和胃组方能提高晚期大肠癌化疗患者的临床疗效,改善中医症状,增强机体免疫力。其可能是通过提高促凋亡蛋白Bax和降低抑凋亡蛋白Bcl-2的表达起到增加化疗疗效、改善患者生活质量的作用。
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  • 图 1  治疗组治疗前后Bcl-2、Bax免疫组化染色(×400)

    图 2  两组患者Bcl-2、Bax蛋白表达的Western blot分析

    表 1  两组患者的临床资料比较 例,X±S

    组别 例数 性别 年龄/岁 体重/kg 原发部位 病理类型
    结肠癌 直肠癌 管状腺癌 黏液腺癌 印戒细胞癌
    治疗组 25 17 8 60.24±7.79 54.74±4.79 10 15 19 5 1
    对照组 25 16 9 60.16±6.97 54.37±4.44 9 16 20 5 0
    下载: 导出CSV

    表 2  两组患者的临床疗效比较 

    组别 例数 CR PR SD PD ORR/% DCR/% Z P
    治疗组 25 0 7 14 4 28 84 -0.612 0.541
    对照组 25 0 6 13 6 24 76
    下载: 导出CSV

    表 3  两组患者的中医证候评分比较 分,X±S

    组别 例数 治疗前 治疗后 t P
    治疗组 25 13.32±1.52 6.04±2.511)2) -1.393 < 0.001
    对照组 25 13.12±1.67 9.52±3.481) -5.645 < 0.001
    t 0.443 -4.058
    P 0.659 < 0.001
    与本组治疗前比较,1)P < 0.001;与对照组比较,2)P < 0.001。
    下载: 导出CSV

    表 4  两组患者的中医证候疗效比较 例(%)

    组别 例数 临床痊愈 显效 有效 无效 总有效率/% χ2 P
    治疗组 25 0 7(28) 13(52) 5(20) 801) 4.367 0.037
    对照组 25 0 4(16) 9(36) 12(48) 52
    与对照组比较,1)P < 0.05。
    下载: 导出CSV

    表 5  两组患者的KPS评分比较 分,X±S

    组别 例数 治疗前 治疗后 t P
    治疗组 25 71.60±5.54 75.60±8.701)2) 2.191 0.038
    对照组 25 69.20±4.93 72.60±9.781) 1.204 0.040
    t 1.618 2.292
    P 0.112 0.046
    与本组治疗前比较,1)P < 0.05;与对照组比较,2)P < 0.05。
    下载: 导出CSV

    表 6  两组患者的Bcl-2、Bax染色光密度值比较 X±S

    组别 例数 Bcl-2 P Bax P
    治疗前 治疗后 治疗前 治疗后
    治疗组 25 0.78±0.05 0.41±0.03 < 0.001 0.52±0.03 0.83±0.04 < 0.001
    对照组 25 0.77±0.04 0.52±0.02 0.045 0.53±0.04 0.68±0.03 0.037
    P 0.801 0.038 0.725 0.046
    下载: 导出CSV

    表 7  两组患者Bcl-2、Bax表达的比较 X±S

    组别 例数 Bcl-2 P Bax P
    治疗前 治疗后 治疗前 治疗后
    治疗组 25 0.89±0.04 0.32±0.02 < 0.001 0.26±0.01 0.79±0.03 < 0.001
    对照组 25 0.88±0.03 0.37±0.03 < 0.001 0.25±0.02 0.67±0.05 < 0.001
    P 0.924 0.047 0.763 0.048
    下载: 导出CSV
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出版历程
收稿日期:  2024-03-23
刊出日期:  2024-11-15

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