首页|14例贝伐珠单抗不良反应的文献回顾

14例贝伐珠单抗不良反应的文献回顾

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目的:分析贝伐珠单抗引起的药品不良反应(ADR)的特征,为临床安全用药提供参考.方法:检索建库至 2023 年 3 月中国知网、万方、维普、PubMed数据库关于贝伐珠单抗ADR的个案报道文献,对患者的性别、年龄、肿瘤类型、ADR的发生时间、累及系统/器官、对症治疗、转归等进行统计分析.结果:纳入14篇贝伐珠单抗ADR的个案报道文献,涉及病例14例.其中,男性5例(35.71%),女性9例(64.29%);年龄范围36~70岁,平均年龄(55.79±10.10)岁;非小细胞肺癌4例(28.57%),结直肠癌 5 例(35.71%),皮肤鳞状细胞癌、卵巢癌、乳腺癌、恶性黑色素瘤及宫颈鳞癌各1例(7.14%).5 例(35.71%)患者在首次用药后发生ADR;4例(28.57%)患者在1个用药周期内发生ADR;3例(21.43%)患者在2个用药周期内发生ADR;2例(14.29%)患者在 3 个用药周期后发生ADR.ADR累及系统/器官包括全身整体疾病、胃肠疾病、心血管疾病、神经系统疾病、皮肤及皮肤附件疾病、代谢及营养疾病、精神疾病、呼吸系统疾病,其中累及多系统/器官的病例为 6 例(42.86%).13 例(92.86%)患者在停药并给予积极对症治疗后均显著好转,1例(7.14%)患者死亡.结论:应加强贝伐珠单抗ADR的临床监测,及时发现ADR并进行对症治疗,以提高临床用药安全性及患者预后.
Literature Review of 14 Cases of Adverse Reactions to Bevacizuma
Objective:To analyze the characteristics of adverse drug reactions(ADR)caused by bevacizumab to provide reference for safe clinical use.Methods:Retrieve case reports of bevacizumab ADR from the databases of China National Knowledge Infrastructure,Wanfang,VIP,and PubMed up to March 2023,and conduct statistical analysis on patients'gender,age,tumor type,occurrence time of ADR,involvement of systems/organs,symptomatic treatment,and outcomes.Results:14 case reports of bevacizumab ADR were included,involving 14 cases.Among them,there were 5 males(35.71% )and 9 females(64.29% );the age range was 36 to 70 years old,with an average age of(55.79±10.10)years;There were 4 cases of non-small cell lung cancer(28.57% ),5 cases of colorectal cancer(35.71% ),1 case of skin squamous cell carcinoma,1 case of ovarian cancer,1 case of breast cancer,1 case of malignant melanoma,and 1 case of cervical squamous cell carcinoma(7.14% ).5 cases(35.71% )of patients developed ADR after their first medication;4 patients(28.57% )experienced ADR within 1 medication cycle;3 patients(21.43% )experienced ADR within 2 medication cycles;2 patients(14.29% )developed ADR after 3 medication cycles.ADR affects systemic diseases,gastrointestinal diseases,cardiovascular diseases,neurological diseases,skin and skin accessory diseases,metabolic and nutritional diseases,mental sickness and respiratory system diseases with 6 cases(42.86% )involving multiple systems/organs.13 patients(92.86% )showed significant improvement in ADR after discontinuing medication and receiving active symptomatic treatment,while 1 patient(7.14% )died.Conclusion:Clinical monitoring of bevacizumab ADR should be strengthened,and ADR should be detected in a timely manner and treated accordingly to improve the safety of clinical medication and patient prognosis.

bevacizumabtumoradverse drug reactionliterature reviewclinical monitoring

崔李平、亢卫华、王利杰、冯钊慧、王秀丽

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焦作市第二人民医院药学部,焦作 454001

贝伐珠单抗 肿瘤 药品不良反应 文献回顾 临床监测

2024

中国合理用药探索
中国执业药师协会

中国合理用药探索

影响因子:0.62
ISSN:2096-3327
年,卷(期):2024.21(12)