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lynparza（olaparib）
Date Action January 2015 Addition to PA March 2015 Annual review and reference update June 2016 Annual editorial review and reference update Policy change from 5.04.52 to 5.21.52 June 2017 Annual editorial review and reference update Addition of unacceptable toxicity to renewal section September 2017 Annual review Addition of recurrent epithelial ovarian, fallopian tube or primary peritoneal cancer Addition of quantity limits Removal of no concurrent therapy with other治疗卵巢癌的药物2018年2月将转移性乳腺癌添加到启动和更新标准中。在新辅助，佐剂或转移性环境中添加BRCA阳性，先前的化学疗法治疗，如果先前必须对先前的内分泌治疗进行治疗，或者必须接受内分泌治疗的治疗，或者被认为是内分泌治疗的不适当候选者，用于内部分泌治疗，用于逐年诊断为672诊断672的培养基，以诊断为672的培训标准。新指示的添加：BRCA的晚期上皮卵巢，输卵管或原发性腹膜癌。Removal of Lynparza 50mg capsules March 2019 Annual review May 2019 Changed quantity limit to 360 tablets per 90 days for both strengths of Lynparza June 2019 Annual review January 2020 Addition of indication: metastatic pancreatic cancer March 2020 Annual review May 2020 Addition of indication: used in combination with bevacizumab for the maintenance treatment of adult patients with advanced epithelial ovarian, fallopian tube或原发性腹膜癌对一线铂化学疗法有完全或部分反应，其癌症为
olaparib-lynparza®-expansion-bevacizumab-avastin ...
重要通知：NCODA开发了这个积极的质量干预平台。该平台旨在作为教育援助，不提供个人的医疗建议，也不能代替合格的医疗保健专业人员的建议。该平台并未涵盖与可能的用途，方向，剂量，预防措施，警告，互动，不良影响或与药物相关的风险有关的所有现有信息。本平台中包含的材料并不构成或暗示NCODA对这种药物的认可，建议或偏爱。ncoda不能确保提供的信息的准确性，并且不承担与其准确性有关的责任。与服用这种药物有关的所有决定均应在指导和合格的医疗保健专业人员的指导下做出。从合格的医疗保健专业人员那里寻求指导是个人的唯一责任。更新了12.19.23