sorafenib (Nexavar)

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Introduction

Trademark: Nexavar, FDA approved 2005

Indications

Adverse effects

Laboratory

Mechanism of action

Manufacturer: Bayer/Onyx

More general terms

References

  1. Prescriber's Letter 13(2): 2006 Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=220215&pb=PRL (subscription needed) http://www.prescribersletter.com
  2. 2.0 2.1 Physician's First Watch, June 3, 2013 David G. Fairchild, MD, MPH, Editor-in-Chief Massachusetts Medical Society http://www.jwatch.org
    Brose MS et al Sorafenib in locally advanced or metastatic patients with radioactive iodine-refractory differentiated thyroid cancer: The phase III DECISION trial. 2013 ASCO Meeting Abstract J Clin Oncol 31, 2013 (suppl; abstr 4) http://meetinglibrary.asco.org/content/112795-132
  3. 3.0 3.1 3.2 Medical Knowledge Self Assessment Program (MKSAP) 16, 17 American College of Physicians, Philadelphia 2012, 2015
  4. 4.0 4.1 FDA News Release: Nov. 22, 2013 FDA approves Nexavar to treat type of thyroid cancer http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm376443.htm
  5. 5.0 5.1 O'Neil A, Short NJ AML: TKI Sorafenib Added to '7+3' Equals EFS Benefit. The multiple kinase inhibitor targets several different pathways important for AML development and maintenance. MedPage Today. Jan 11, 2018 https://www.medpagetoday.com/reading-room/asco/hematologic-malignancies/70405
    Rollig C, et al The addition of sorafenib to standard AML treatment results in a substantial reduction in relapse risk and improved survival. Updated results from long-term follow-up of the randomized- controlled Soraml Trial. American Society of Hematology (ASH) 2017; Abstract 721.
  6. 6.0 6.1 NEJM Knowledge+ Nephrology/Urology

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