Drug review: Pazopanib. (19th April 2018)
- Record Type:
- Journal Article
- Title:
- Drug review: Pazopanib. (19th April 2018)
- Main Title:
- Drug review: Pazopanib
- Authors:
- Miyamoto, Shingo
Kakutani, Shigenori
Sato, Yujiro
Hanashi, Akira
Kinoshita, Yoshitaka
Ishikawa, Akira - Abstract:
- Abstract : We present the results of clinical trials as well as the pharmacological action of pazopanib, with the aim of evaluating its current state by examining various associated issues. Abstract: Pazopanib (Votrient®) is an oral small-molecule multi-kinase inhibitor that primarily inhibits vascular endothelial growth factor receptor-1, -2 and -3, platelet endothelial growth factor receptor-α, and -β, and the stem-cell factor receptor c-kit. In preliminary experiments using angiogenesis models with mice and rabbits, pazopanib inhibited angiogenesis caused by combined vascular endothelial growth factor and basic fibroblast growth factor. Although pazopanib was developed as a therapeutic agent against various tumors, it is currently approved in many countries for advanced soft-tissue sarcoma and renal cell carcinoma. The importance of pazopanib has been acknowledged, with positive results demonstrated in large-scale clinical trials involving patients with soft-tissue sarcoma and renal cell carcinoma. However, adverse events such as liver dysfunction and hypertension are common, often necessitating treatment discontinuation. These adverse events are generally manageable, and from the perspective of health-related quality of life and cost-effectiveness, pazopanib provides an improvement in quality-adjusted life years and decreases the treatment cost compared with other alternatives. In this review, we present the results of clinical trials and discuss the pharmacologicalAbstract : We present the results of clinical trials as well as the pharmacological action of pazopanib, with the aim of evaluating its current state by examining various associated issues. Abstract: Pazopanib (Votrient®) is an oral small-molecule multi-kinase inhibitor that primarily inhibits vascular endothelial growth factor receptor-1, -2 and -3, platelet endothelial growth factor receptor-α, and -β, and the stem-cell factor receptor c-kit. In preliminary experiments using angiogenesis models with mice and rabbits, pazopanib inhibited angiogenesis caused by combined vascular endothelial growth factor and basic fibroblast growth factor. Although pazopanib was developed as a therapeutic agent against various tumors, it is currently approved in many countries for advanced soft-tissue sarcoma and renal cell carcinoma. The importance of pazopanib has been acknowledged, with positive results demonstrated in large-scale clinical trials involving patients with soft-tissue sarcoma and renal cell carcinoma. However, adverse events such as liver dysfunction and hypertension are common, often necessitating treatment discontinuation. These adverse events are generally manageable, and from the perspective of health-related quality of life and cost-effectiveness, pazopanib provides an improvement in quality-adjusted life years and decreases the treatment cost compared with other alternatives. In this review, we present the results of clinical trials and discuss the pharmacological action of pazopanib, with the aim of evaluating its current state by examining various associated issues. … (more)
- Is Part Of:
- Japanese journal of clinical oncology. Volume 48:Number 6(2018)
- Journal:
- Japanese journal of clinical oncology
- Issue:
- Volume 48:Number 6(2018)
- Issue Display:
- Volume 48, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 48
- Issue:
- 6
- Issue Sort Value:
- 2018-0048-0006-0000
- Page Start:
- 503
- Page End:
- 513
- Publication Date:
- 2018-04-19
- Subjects:
- pazopanib -- soft tissue sarcoma -- renal cell carcinoma
Oncology -- Periodicals
Cancer -- Periodicals
616.994005 - Journal URLs:
- http://jjco.oupjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/jjco/hyy053 ↗
- Languages:
- English
- ISSNs:
- 0368-2811
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4651.378000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12397.xml