Long-term effects of BRAF inhibitors in melanoma treatment: friend or foe?. (April 2014)
- Record Type:
- Journal Article
- Title:
- Long-term effects of BRAF inhibitors in melanoma treatment: friend or foe?. (April 2014)
- Main Title:
- Long-term effects of BRAF inhibitors in melanoma treatment: friend or foe?
- Authors:
- Sloot, Sarah
Fedorenko, Inna V
Smalley, Keiran SM
Gibney, Geoffrey T - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p>The clinical development of selective BRAF inhibitors for metastatic <italic>BRAF</italic> V600 mutant melanoma patients has been a major breakthrough in targeted therapeutics. Objective response rates of approximately 50% have been observed in the Phase III studies of the BRAF inhibitors vemurafenib and dabrafenib. The side effects can be relatively common, including proliferative skin toxicities. The latter range from hyperkeratosis and keratoacanthomas (KAs) to squamous cell carcinomas (SCCs) and new primary melanomas. In addition, case reports on the emergence of gastric/colonic polyps and <italic>RAS</italic> mutant malignancies have been described during BRAF inhibitor therapy. These events have been attributed to paradoxical activation of the MAPK pathway in <italic>BRAF</italic> wild-type cells exposed to selective BRAF inhibitors in addition to increased RAS activity. Combined BRAF and MEK inhibition appears to improve clinical outcomes and reduce cutaneous proliferation events as fewer KAs and SCCs have been observed with combination therapy. Next-generation pan-RAF inhibitors ('paradox breakers') and ERK inhibitors may further enhance clinical activity in metastatic <italic>BRAF</italic>-mutant melanoma patients and mitigate this paradoxical oncogenesis. Further investigation into the potential long-term effects of selective BRAF inhibitors is warranted as expanded use of these agents is expected<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p>The clinical development of selective BRAF inhibitors for metastatic <italic>BRAF</italic> V600 mutant melanoma patients has been a major breakthrough in targeted therapeutics. Objective response rates of approximately 50% have been observed in the Phase III studies of the BRAF inhibitors vemurafenib and dabrafenib. The side effects can be relatively common, including proliferative skin toxicities. The latter range from hyperkeratosis and keratoacanthomas (KAs) to squamous cell carcinomas (SCCs) and new primary melanomas. In addition, case reports on the emergence of gastric/colonic polyps and <italic>RAS</italic> mutant malignancies have been described during BRAF inhibitor therapy. These events have been attributed to paradoxical activation of the MAPK pathway in <italic>BRAF</italic> wild-type cells exposed to selective BRAF inhibitors in addition to increased RAS activity. Combined BRAF and MEK inhibition appears to improve clinical outcomes and reduce cutaneous proliferation events as fewer KAs and SCCs have been observed with combination therapy. Next-generation pan-RAF inhibitors ('paradox breakers') and ERK inhibitors may further enhance clinical activity in metastatic <italic>BRAF</italic>-mutant melanoma patients and mitigate this paradoxical oncogenesis. Further investigation into the potential long-term effects of selective BRAF inhibitors is warranted as expanded use of these agents is expected in patients with BRAF-mutant melanoma and other malignancies.</p> </abstract> … (more)
- Is Part Of:
- Expert opinion on pharmacotherapy. Volume 15:Number 5(2014)
- Journal:
- Expert opinion on pharmacotherapy
- Issue:
- Volume 15:Number 5(2014)
- Issue Display:
- Volume 15, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 15
- Issue:
- 5
- Issue Sort Value:
- 2014-0015-0005-0000
- Page Start:
- 589
- Page End:
- 592
- Publication Date:
- 2014-04
- Subjects:
- Chemotherapy -- Periodicals
615.5805 - Journal URLs:
- http://informahealthcare.com/ ↗
http://www.tandfonline.com/toc/ieop20/current ↗
http://informahealthcare.com ↗
http://titania.ashley-pub.com/vl=5663459/cl=52/nw=1/rpsv/journal/journal6_home.htm ↗ - DOI:
- 10.1517/14656566.2014.881471 ↗
- Languages:
- English
- ISSNs:
- 1465-6566
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002956
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4012.xml