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190504 r ||| eng |
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|a Ho, Chuong
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|a BRAF targeted therapy for patients with melanoma and active brain metastases
|h Elektronische Ressource
|b a review of clinical effectiveness
|c Chuong Ho, Lorna Adcock
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|a Version 1.0
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|a Ottawa (ON)
|b Canadian Agency for Drugs and Technologies in Health
|c 2017, October 18, 2017
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|a 1 PDF file (16 pages)
|b illustrations
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|a Includes bibliographical references
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|a Melanoma / secondary
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|a Antineoplastic Agents
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|a Antineoplastic Combined Chemotherapy Protocols
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|a Canada
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|a Melanoma / drug therapy
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|a Treatment Outcome
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|a Proto-Oncogene Proteins B-raf / antagonists & inhibitors
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|a Protein Kinase Inhibitors
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|a Adcock, Lorna
|e [author]
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a CADTH rapid response report: summary with critical appraisal
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|u https://www.ncbi.nlm.nih.gov/books/NBK513219
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a Skin cancer is the most common cancer in Canada, with about 6,500 new cases of skin malignant melanoma reported in 2014, and 1250 Canadians expected to die from it in 2017. Approximately 40-60% of melanomas contain a mutation in the gene that encodes BRAF, which leads to constitutive activation of downstream signaling in the MAP (mitogen-activated protein) kinase pathway. This Rapid Response report aims to review the clinical effectiveness and safety of dabrafenib plus trametinib and cobimetinib plus vemurafenib for patients with BRAF (human gene that encodes a protein called B-Raf) mutation positive metastatic melanoma with active brain metastasis
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