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中国科学技术大学附属第一医院(安徽省立医院)药学部/安徽省药品临床综合评价技术中心,合肥 230001
主管药师,硕士。研究方向:临床药学。电话:0551-62283341。E-mail:94027845@qq.com
主任药师,硕士生导师。研究方向:医院管理、临床药学、药物经济学。电话:0551-62283008。E-mail:1649441800@qq.com
收稿日期:2022-05-16,
修回日期:2022-08-26,
纸质出版日期:2022-11-30
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季鹏,宁丽娟,陈泳伍,等.白蛋白结合型紫杉醇治疗晚期非小细胞肺癌的有效性和安全性[J].中国药房,2022,33(22):2762-2765.
JI Peng,NING Lijuan,CHEN Yongwu,et al.Efficacy and safety of albumin-bound paclitaxel in the treatment of advanced non-small cell lung cancer[J].ZHONGGUO YAOFANG,2022,33(22):2762-2765.
季鹏,宁丽娟,陈泳伍,等.白蛋白结合型紫杉醇治疗晚期非小细胞肺癌的有效性和安全性[J].中国药房,2022,33(22):2762-2765. DOI: 10.6039/j.issn.1001-0408.2022.22.15.
JI Peng,NING Lijuan,CHEN Yongwu,et al.Efficacy and safety of albumin-bound paclitaxel in the treatment of advanced non-small cell lung cancer[J].ZHONGGUO YAOFANG,2022,33(22):2762-2765. DOI: 10.6039/j.issn.1001-0408.2022.22.15.
目的
2
观察白蛋白结合型紫杉醇治疗晚期非小细胞肺癌(NSCLC)的有效性及安全性。
方法
2
纳入我院2018年1月-2021年12月收治的晚期NSCLC患者的临床资料,根据其所用化疗方案分为白蛋白结合型紫杉醇组和紫杉醇组,每组100例。两组患者均接受含注射用紫杉醇(白蛋白结合型)或紫杉醇注射液的化疗方案治疗至少2个周期(每21 d为1个周期),比较两组患者的无进展生存期(PFS)和疗效,并记录毒副反应发生情况。
结果
2
白蛋白结合型紫杉醇组患者共完成化疗430个周期,平均4.3个周期;紫杉醇组患者共完成化疗476个周期,平均4.8个周期。白蛋白结合型紫杉醇组患者的中位PFS(4.0个月)、有效率(13.00%)与紫杉醇组(4.0个月、9.00%)比较,差异均无统计学意义(
P
>0.05),其疾病控制率(99.00%)显著高于紫杉醇组(89.00%),其白细胞减少、中性粒细胞减少、血小板减少、贫血、感觉神经病变、乏力、恶心呕吐、关节肌痛的发生率均显著低于紫杉醇组(
P
<0.05)。
结论
2
白蛋白结合型紫杉醇治疗晚期NSCLC的疗效较好,比普通紫杉醇能更好地控制疾病的进展,且安全性更高。
OBJECTIVE
2
To observe the efficacy and safety of albumin-bound paclitaxel in the treatment of advanced non-small cell lung cancer (NSCLC).
METHODS
2
Clinical data of patients with advanced NSCLC treated in our hospital from January 2018 to December 2021 were selected. According to their chemotherapy regimen,they were divided into albumin-bound paclitaxel group and paclitaxel group, with 100 patients in each group. Both groups received chemotherapy regimen containing Paclitaxel for injection (albumin-bound) or Paclitaxel injection for at least 2 cycles (every 21 days as a cycle). The progression-free survival (PFS) and efficacy of the two groups were compared,and the occurrence of toxic and side effects were recorded.
RESULTS
2
The patients in albumin-bound paclitaxel group completed 430 cycles of chemotherapy, with an average of 4.3 cycles; patients in paclitaxel group completed 476 cycles of chemotherapy, with an average of 4.8 cycles. The median PFS (4.0 months) and the response rate (13.00%) of albumin-bound paclitaxel group were not significantly different from those of paclitaxel group (4.0 months,9.00%) (
P
>0.05). The disease control rate (99.00%) was significantly higher than that in paclitaxel group (89.00%), and the incidences of leukopenia, neutropenia, thrombocytopenia,anemia, sensory neuropathy, fatigue,nausea and vomiting,joint myalgia in albumin-bound paclitaxel group were significantly lower than those in paclitaxel group (
P
<0.05).
CONCLUSIONS
2
Albumin-bound paclitaxel is effective in the treatment of advanced NSCLC, and it can better control the progression of the disease and is safer than ordinary paclitaxel.
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