首页|阿帕鲁胺联合DP方案治疗转移性去势抵抗性前列腺癌的临床效果

阿帕鲁胺联合DP方案治疗转移性去势抵抗性前列腺癌的临床效果

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目的 探究阿帕鲁胺联合DP方案(多西他赛+泼尼松)治疗转移性去势抵抗性前列腺癌的临床效果.方法 选取2020年1月至2022年1月郑州大学第一附属医院诊治的82例转移性去势抵抗性前列腺癌患者作为研究对象.根据治疗方法分组,对照组42例接受DP方案治疗,治疗组40例接受阿帕鲁胺联合DP方案治疗.比较两组临床疗效、血清前列腺特异性抗原及睾酮水平、不良反应、生存情况.结果 治疗组客观缓解率(70.00%)高于对照组(47.62%)(P<0.05).治疗组治疗后前列腺特异性抗原和睾酮水平均低于对照组(P<0.05).两组患者仅对照组发生2例Ⅲ级消化道反应(恶心),其余均为Ⅰ~Ⅱ级轻度不良反应.治疗组发生消化道反应(恶心)16例(40.00%)、白细胞降低11例(27.50%)、脱发8例(20.00%)、乏力6例(15.00%)、肝毒性4例(10.00%)、中粒性细胞减少2例(5.00%);对照组发生消化道反应(恶心)14例(33.33%)、白细胞降低4例(9.52%)、脱发9例(21.43%)、乏力5例(11.90%)、肝毒性2例(4.76%)、中粒性细胞减少1例(2.38%),两组比较差异无统计学意义(P>0.05).治疗组和对照组中位前列腺特异性抗原无进展生存期分别为8.4个月(95%CI:11.87~13.88)、7.0个月(95%CI:10.57~12.72),治疗组前列腺特异性抗原无进展生存期长于对照组(P<0.05).结论 阿帕鲁胺联合DP方案治疗转移性去势抵抗性前列腺癌效果明显,能有效改善前列腺特异性抗原及睾酮水平,未增加不良反应,可延长前列腺特异性抗原无进展生存期.
Clinical Efficacy of Apalutamide Combined with DP Chemotherapy Regimen for Metastatic Castration-Resistant Prostate Cancer
Objective To investigate the clinical efficacy of apalutamide combined with docetaxel+prednisone(DP)chemotherapy regimen for metastatic castration-resistant prostate cancer.Methods Eighty-two patients with metastatic castration-resistant prostate cancer in the First Affiliated Hospital of Zhengzhou University from January 2020 to January 2022 were enrolled,and classified into two groups according to different treatment methods.Control group(42 cases)adopted DP chemotherapy regimen,while treatment group(40 cases)was given apalutamide combined with DP chemotherapy.Then the clinical outcomes,serum prostate-specific antigen and testosterone levels,adverse effects,and survival rate were compared between two groups.Results The overall response rate was 70.00%in treatment group,which was higher than 47.62%in control group(P<0.05).After treatment,the levels of prostate specific antigen and testosterone in treatment group were lower than those in control group(P<0.05).Only 2 patients in control group developed acute grade Ⅲ gastrointestinal toxicity(nausea and vomiting),and the rest adverse reactions were mild(degree Ⅰ-Ⅱ).In treatment group,gastrointestinal toxicity(nausea and vomiting)occurred in 16 cases(40.00%),leukopenia in 11 cases(27.50%),alopecia in 8 cases(20.00%),fatigue in 6 cases(15.00%),hepatotoxicity in 4 cases(10.00%),and granulocytopenia in 2 cases(5.00%).In control group,gastrointestinal toxicity(nausea and vomiting)occurred in 14 cases(33.33%),leukopenia in 4 cases(9.52%),alopecia in 9 cases(21.43%),fatigue in 5 cases(11.90%),hepatotoxicity in 2 cases(4.76%),and granulocytopenia in 1 case(2.38%).The total adverse reaction rate yielded no statistical difference between two groups(P>0.05).The median prostate-specific antigen progression-free survival in the treatment and control groups was 8.4 months(95%CI:11.87-13.88)and 7.0 months(95%CI:10.57-12.72),respectively,and prostate-specific survival was longer than the control group(P<0.05).Conclusion Application of apalutamide combined with DP chemotherapy regimen for metastatic castration-resistant prostate cancer can effectively improve the prostate specific antigen and testosterone levels without increasing adverse reactions,thus prolonging prostate specific antigen progression free survival.

apalutamidedocetaxelprednisonemetastatic castration-resistant prostate cancerprostate specific antigen

李思思、董亚娟、吴培

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郑州大学第一附属医院泌尿外科,河南郑州 450000

阿帕鲁胺 多西他赛 泼尼松 转移性去势抵抗性前列腺癌 前列腺特异性抗原

2024

河南医学研究
河南省医学科学院

河南医学研究

影响因子:0.979
ISSN:1004-437X
年,卷(期):2024.33(13)
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