[Guidelines for pharmaceutical care of endocrine therapeutics for breast cancer(2023 edition)].

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引用次数: 0

Abstract

Endocrine therapy is one of the primary treatment methods for hormone receptor-positive breast cancer patients. As of June 1 2023, the National Medical Product Administration has approved 56 drugs related to endocrine therapy in patients with HR+ /HER-2- breast cancer (including generic drugs that have passed the consistency evaluation), including 44 endocrine drugs which can be categorized according to their mechanisms of action into selective estrogen receptor modulators, selective estrogen receptor down-regulators, aromatase inhibitors, luteinizing hormone-releasing hormone analogs, and progestogens and 12 targeted drugs for combined with endocrine therapy, including CDK4/6 inhibitors, mTOR inhibitors, and HDAC inhibitors. The different pharmacological characteristics, mechanisms of action, and long-term medication factors of breast cancer endocrine therapy-related drugs can directly affect patients' medication adherence and medication safety. To standardize the pharmaceutical care of endocrine therapy drugs for breast cancer and promote rational use in clinical settings, the Oncology Specialty Pharmacist Subcommittee, in conjunction with multidisciplinary experts nationwide, has developed the "Guidelines for pharmaceutical care of endocrine therapy drugs for breast cancer (2023 edition)". The guidelines is based on clinical evidence-based evidence, relevant regulations of pharmaceutical management, and pharmaceutical care practices. The Delphi method and expert interviews were used to formulate the guidelines. The GRADE approach was used for assessing the certainty of evidence. This guideline mainly focuses on endocrine therapy for HR+ /HER-2- breast cancer patients. Due to space constraints, HER-2 positive targeted drugs were not included in the guideline. It covers 6 dimensions and 22 key problems of pharmaceutical care in the whole process of drug therapy, providing a scientific basis for pharmacists to carry out pharmaceutical care of such drugs.

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[乳腺癌内分泌治疗药学服务指南(2023年版)]。
内分泌治疗是癌症激素受体阳性患者的主要治疗方法之一。截至2023年6月1日,国家药品监督管理局已批准56种与HR+/HER-2-乳腺癌症患者内分泌治疗相关的药物(包括通过一致性评价的仿制药),其中44种内分泌药物可根据作用机制分类为选择性雌激素受体调节剂,选择性雌激素受体下调因子、芳香化酶抑制剂、黄体生成素释放激素类似物和孕激素,以及12种用于联合内分泌治疗的靶向药物,包括CDK4/6抑制剂、mTOR抑制剂和HDAC抑制剂。癌症内分泌治疗相关药物的不同药理特征、作用机制和长期用药因素可直接影响患者的用药依从性和用药安全性。为规范癌症内分泌治疗药物的药学服务,促进临床合理使用,肿瘤专科药师小组委员会联合全国多学科专家,制定了《癌症内分泌治疗药物药学服务指南(2023年版)》。该指南基于临床循证证据、药物管理的相关规定和药物护理实践。采用德尔菲法和专家访谈来制定指导方针。GRADE方法用于评估证据的确定性。本指南主要关注HR+/HER-2乳腺癌症患者的内分泌治疗。由于篇幅限制,HER-2阳性靶向药物未纳入指南。它涵盖了药物治疗全过程中药学护理的6个维度和22个关键问题,为药剂师开展此类药物的药学护理提供了科学依据。
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来源期刊
中华肿瘤杂志
中华肿瘤杂志 Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
10433
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