首页|期刊导航|中国临床药理学杂志|哌柏西利联合曲妥珠单抗治疗HR+/HER-2+乳腺癌的临床研究

哌柏西利联合曲妥珠单抗治疗HR+/HER-2+乳腺癌的临床研究OA

Clinical trial of palbociclib combined with trastuzumab in the treatment of HR+/HER-2+breast cancer

中文摘要英文摘要

目的 探讨哌柏西利胶囊联合注射用曲妥珠单抗治疗既往接受曲妥珠单抗治疗后出现疾病进展的激素受体阳性(HR+)/人表皮生长因子受体2阳性(HER-2+)乳腺癌的临床疗效和安全性.方法 将HR+/HER-2+乳腺癌患者根据治疗方法分为对照组和试验组.对照组用注射用曲妥珠单抗静脉滴注治疗,首次剂量为8 mg·kg-1,于治疗第1 d缓慢静脉滴注(滴注时间≥90 min);此后维持剂量为6 mg·kg-1,每28 d为1个治疗周期,于每个周期第1 d静脉滴注(滴注时间≥30 min);试验组采用哌柏西利胶囊联合注射用曲妥珠单抗治疗,注射用曲妥珠单抗用法同对照组,哌柏西利胶囊采用口服给药方式,根据患者状态决定初始量从125 mg或100 mg(如果不良反应严重则进行减量)持续用药21 d,停药7 d,28 d为1个治疗周期.2组均治疗3个疗程并进行随访.比较2组患者的临床疗效、肿瘤标志物、血清学指标、免疫功能、磷脂酰肌醇-3-激酶(PI3K)/蛋白激酶B(AKT)通路相关蛋白表达、生存质量、安全性评价及预后情况.结果 共纳入患者78例,对照组入组41例,试验组入组37例.治疗后,试验组和对照组的临床有效率分别为40.54%(15例/37例)和17.07%(7例/41例)(P<0.05).试验组和对照组的的中位无进展生存期(PFS)分别为24.5个月和14.3个月;糖类抗原15-3(CA15-3)分别为(36.72±5.64)和(40.92±6.73)IU·mL-1;血管内皮生长因子(VEGF)水平分别为(86.22±12.32)和(95.26±12.15)pg·mL-1;分化簇 3 阳性 T 细胞(CD3+)分别为(50.16±7.12)%和(46.30±7.16)%;p-AKT 蛋白相对表达水平分别为0.58±0.12和0.64±0.11;健康调查简易量表(SF-36)评分为分别(72.29±9.49)和(67.18±8.93)分,上述指标2组间比较,在统计学上差异均有统计学意义(P<0.05,P<0.01,P<0.001).2组患者出现的药物不良反应包括血小板下降、白细胞下降、中性粒细胞减少、恶心呕吐、肝功能异常,试验组和对照组药物不良反应发生率分别为72.97%(27例/37例)和70.73%(29例/41例),在统计学上差异无统计学意义(P>0.05).结论 哌柏西利胶囊联合注射用曲妥珠单抗治疗HR+/HER-2+乳腺癌患者疗效确切,能更有效降低肿瘤标志物水平,显著延长无进展生存期,改善患者的生存质量,且不增加总体不良反应.

Objective To evaluate the clinical efficacy and safety of palbociclib capsules combined with trastuzumab injection in the treatment of hormone receptor positive(HR+)/human epidermal growth factor receptor 2 positive(HER-2+)breast cancer patients who had progressed after prior trastuzumab therapy.Methods Patients with HR+/HER-2+breast cancer were divided into control group and treatment group.The control group was treated with intravenous infusion of trastuzumab injection[the initial dose was 8 mg·kg-1,administered slowly intravenously on the first day of treatment(infusion time ≥ 90 min);thereafter,the maintenance dose was 6 mg·kg-1,with 28 days as one treatment cycle,and intravenous infusion was administered on the first day of each cycle(infusion time ≥ 30 min)].The treatment group was treated with trastuzumab injection combined with palbociclib capsules,the administration of trastuzumab was the same as that of the control group,and palbociclib capsules was administered orally.The initial dose was determined based on the patient's condition,ranging from 125 mg to 100 mg(if the adverse reactions were severe,the dose would be reduced),and the treatment was continued for 21 days,followed by a 7-day withdrawal,with a total of 28 days as one treatment cycle.Both groups were treated for three courses and followed up.The clinical efficacy,tumor markers,serological indicators,immune function,expression of phosphatidylinositol-3-kinase(PI3K)/protein kinase B(AKT)pathway-related proteins,quality of life,safety evaluation and prognosis of the two groups of patients were compared.Results A total of 78 patients were enrolled,with 41 cases in the control group and 37 cases in the treatment group.After treatment,the total effective rate of the treatment group and the control group were 40.54%(15 cases/37 cases)and 17.07%(7 cases/41 cases),(P<0.05).The median progression free survival(PFS)of the treatment group and the control group were 24.5 and 14.3 months,respectively;the cancer antigen 15-3(CA15-3)levels were(36.72±5.64)and(40.92±6.73)IU·mL-1,respectively;the levles of vascular endothelial growth factor(VEGF)were(86.22±12.32)and(95.26±12.15)pg·mL-1,respectively;the cluster of differentiation 3 positive(CD3+)percentages were(50.16±7.12)%and(46.30±7.16)%,respectively;the relative expression levels of p-AKT protein were 0.58±0.12 and 0.64±0.1 1,respectively;the short form 36 health survey questionnaire(SF-36)scores werr(72.29±9.49)and(67.18±8.93,)points,respectively.The differences of above indexes were all statistically significant(P<0.05,P<0.01,P<0.001).The overall incidence of drug adverse reactions(including thrombocytopenia,leukopenia,neutropenia,nausea and vomiting,and abnormal liver function)was 72.97%(27 cases/37 cases)in the treatment group and 70.73%(29 cases/41 cases)in the control group,with no statistically significant difference(P>0.05).Conclusion Palbociclib capsules combined with trastuzumab injection has a definite therapeutic effect in HR+/HER-2+breast cancer patients.It can more effectively reduce tumor marker levels,significantly prolong PFS,improve quality of life,and does not increase overall adverse reactions.

武欣欣;梁良

聊城市人民医院 乳腺甲状腺外科,山东聊城 252000聊城市人民医院 药学部,山东聊城 252000

医药卫生

哌柏西利胶囊注射用曲妥珠单抗激素受体阳性人表皮生长因子受体2阳性乳腺癌免疫功能

palbociclib capsulestrastuzumab injectionhormone receptor positivepositive human epidermal growth factor receptor 2breast cancerimmune function

《中国临床药理学杂志》 2026 (8)

1082-1089,8

10.13699/j.cnki.1001-6821.2026.08.006

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