度伐利尤单抗
外观
单克隆抗体 | |
---|---|
种类 | 完整抗体 |
目标 | CD274 |
临床资料 | |
商品名 | Imfinzi(英飞凡) |
其他名称 | MEDI4736, MEDI-4736 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a617030 |
核准状况 | |
怀孕分级 | |
给药途径 | 静脉给药 |
ATC码 | |
法律规范状态 | |
法律规范 |
|
识别信息 | |
CAS号 | 1428935-60-7 |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider |
|
UNII | |
KEGG | |
化学信息 | |
化学式 | C6502H10018N1742O2024S42 |
摩尔质量 | 146,322.36 g·mol−1 |
度伐利尤单抗(Durvalumab [4],商品名Imfinzi,中文商品名英飞凡)是一种用于治疗癌症的完全人源化抗PD-L1单克隆抗体。该药由阿斯利康全资子公司MedImmune研发。 [5]它是一种人类免疫球蛋白G1κ(IgG1κ)单克隆抗体,可阻断PD-L1与PD-1(CD279)。[6]
临床应用
[编辑]NMPA于2019年12月批准该药用于铂类化疗联合放疗失败的III期非小细胞肺癌的治疗。[7]
临床试验
[编辑]度伐利尤单抗的ⅠB期临床试验结果表明该药对非小细胞肺癌(NSCLC)具有抑制作用,[8]该药另一项关于晚期转移性膀胱癌适应症的Ⅰ期临床试验则被FDA纳入快速审批通道。[6][9]度伐利尤单抗联合吉非替尼治疗小细胞肺癌的Ⅰ期临床试验结果表明该联合用药方案具有很好的疗效。[10]目前,该药正在进行一项与TLR 7/8激动剂(MEDI 9197)联合治疗实体瘤的Ⅰ期临床试验[11]以及一项与HPV疫苗(MEDI 0457)联合治疗HPV相关的复发/转移性头颈癌的Ⅱ期临床试验。[12]
2017年7月,阿斯利康宣布,度伐利尤单抗用于非小细胞肺癌一线治疗的Ⅲ期临床试验未能达到预期终点。 [13]
2017年11月,Ⅲ期双盲临床试验表明了度伐利尤单抗对III期非小细胞肺癌具有一定疗效。[14]
参考文献
[编辑]- ^ 1.0 1.1 Durvalumab (Imfinzi) Use During Pregnancy. Drugs.com. 30 August 2019 [7 February 2020]. (原始内容存档于2021-08-29).
- ^ 2.0 2.1 Imfinzi- durvalumab injection, solution. DailyMed. 5 June 2020 [30 September 2020]. (原始内容存档于2021-08-28).
- ^ Imfinzi EPAR. European Medicines Agency (EMA). [30 September 2020]. (原始内容存档于2021-08-28).
- ^ International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 112 (PDF). WHO Drug Information. 2014, 28 (4) [2020-12-15]. (原始内容存档 (PDF)于2021-08-28).
- ^ Research, Center for Drug Evaluation and. Approved Drugs - Durvalumab (Imfinzi). www.fda.gov. [2017-05-06]. (原始内容存档于2017-05-08).
- ^ 6.0 6.1 Syn, Nicholas L; Teng, Michele W L; Mok, Tony S K; Soo, Ross A. De-novo and acquired resistance to immune checkpoint targeting. The Lancet Oncology. 2017, 18 (12): e731–e741. PMID 29208439. doi:10.1016/s1470-2045(17)30607-1.
- ^ 阿斯利康PD-L1抑制剂度伐利尤单抗注射液在华获批. 阿斯利康中国. 2019-12-12.
- ^ Astrazeneca's combination of durvalumab with tremelimumab shows clinical activity in non-small cell lung cancer irrespective of PD-L1 status. Feb 2016. [2020-12-15]. (原始内容存档于2016-02-15).
- ^ AstraZeneca's (AZN) Durvalumab Granted FDA Breakthrough Therapy Designation (页面存档备份,存于互联网档案馆). StreeInsider.com Corporate News, FDA, Management Comments. 17 February 2016.
- ^ Promising Drug for Lung Cancer and Mesothelioma Patients. 19 May 2016 [2020-12-15]. (原始内容存档于2021-08-28).
- ^ Clinical trial number NCT02556463 for "A Study of MEDI9197 in Subjects With Solid Tumors or CTCL and in Combination With Durvalumab and/or Palliative Radiation in Subjects With Solid Tumors" at ClinicalTrials.gov
- ^ Clinical trial number NCT03162224? for "Safety and Efficacy of MEDI0457 and Durvalumab in Patients With HPV Associated Recurrent/Metastatic Head and Neck Cancer" at ClinicalTrials.gov
- ^ AstraZeneca reports initial results from the ongoing MYSTIC trial in Stage IV lung cancer. www.astrazeneca.com. [2020-12-15]. (原始内容存档于2021-08-28).
- ^ AstraZeneca presents superior progression-free survival for Imfinzi in the PACIFIC trial of patients with locally-advanced unresectable lung cancer at ESMO 2017 Congress. www.astrazeneca.com. Sep 2017 [2020-12-15]. (原始内容存档于2021-08-28).
外部链接
[编辑]- Durvalumab. Drug Information Portal. U.S. National Library of Medicine. [2020-12-15]. (原始内容存档于2021-12-12).
- Durvalumab. NCI Drug Dictionary. National Cancer Institute. [2020-12-15]. (原始内容存档于2021-08-28).
- Durvalumab. National Cancer Institute. [2020-12-15]. (原始内容存档于2021-08-28).