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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 2
2008 1
2009 1
2010 2
2011 4
2012 31
2013 35
2014 43
2015 40
2016 47
2017 35
2018 23
2019 28
2020 25
2021 23
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355 results

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2 articles found by citation matching

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Page 1
Melanoma.
Schadendorf D, van Akkooi ACJ, Berking C, Griewank KG, Gutzmer R, Hauschild A, Stang A, Roesch A, Ugurel S. Schadendorf D, et al. Lancet. 2018 Sep 15;392(10151):971-984. doi: 10.1016/S0140-6736(18)31559-9. Lancet. 2018. PMID: 30238891 Review.
Cutaneous melanoma causes 55 500 deaths annually. The incidence and mortality rates of the disease differ widely across the globe depending on access to early detection and primary care. ...Treatments that target B-Raf proto-oncogene serine/threonine-kinase (BRAF)(V
Cutaneous melanoma causes 55 500 deaths annually. The incidence and mortality rates of the disease differ widely across the globe dep
Tolerability of BRAF/MEK inhibitor combinations: adverse event evaluation and management.
Heinzerling L, Eigentler TK, Fluck M, Hassel JC, Heller-Schenck D, Leipe J, Pauschinger M, Vogel A, Zimmer L, Gutzmer R. Heinzerling L, et al. ESMO Open. 2019 May 23;4(3):e000491. doi: 10.1136/esmoopen-2019-000491. eCollection 2019. ESMO Open. 2019. PMID: 31231568 Free PMC article. Review.
The inhibition of the mitogen-activated protein kinases signalling pathway through combined use of BRAF and MEK inhibitors (BRAFi+MEKi) represents an established therapeutic option in patients with BRAF-mutated, advanced melanoma. ...Based on data from confir …
The inhibition of the mitogen-activated protein kinases signalling pathway through combined use of BRAF and MEK inhibitors (BR …
Cutaneous Adverse Events of Anti-PD-1 Therapy and BRAF Inhibitors.
Gnanendran SS, Turner LM, Miller JA, Hwang SJE, Miller AC. Gnanendran SS, et al. Curr Treat Options Oncol. 2020 Mar 19;21(4):29. doi: 10.1007/s11864-020-0721-7. Curr Treat Options Oncol. 2020. PMID: 32193712 Review.
This transition from cytotoxic chemotherapy has yielded improvements in both survival and quality of life; yet despite their therapeutic advantages, these treatments have been associated with a diverse range of cutaneous adverse events (AEs). These range from relati …
This transition from cytotoxic chemotherapy has yielded improvements in both survival and quality of life; yet despite their therapeutic adv …
Cutaneous melanoma.
Tasdogan A, Sullivan RJ, Katalinic A, Lebbe C, Whitaker D, Puig S, van de Poll-Franse LV, Massi D, Schadendorf D. Tasdogan A, et al. Nat Rev Dis Primers. 2025 Apr 3;11(1):23. doi: 10.1038/s41572-025-00603-8. Nat Rev Dis Primers. 2025. PMID: 40180935 Review.
Cutaneous melanoma is a common cancer in Australia and New Zealand, Europe, and North America, and its incidence is still increasing in many regions. ...Cutaneous melanoma treatment has improved considerably over the past decade with the discovery and development of
Cutaneous melanoma is a common cancer in Australia and New Zealand, Europe, and North America, and its incidence is still increasing
Cutaneous Melanoma: A Review.
Joshi UM, Kashani-Sabet M, Kirkwood JM. Joshi UM, et al. JAMA. 2025 Dec 16;334(23):2113-2125. doi: 10.1001/jama.2025.13074. JAMA. 2025. PMID: 40853557 Review.
For stage III disease, recurrence risk is decreased with nivolumab (HR, 0.72 [95% CI, 0.60-0.86]), pembrolizumab (HR, 0.61 [95% CI, 0.51-0.72]), or BRAF + MEK inhibitor therapy (dabrafenib + trametinib) (HR, 0.52 [95% CI, 0.43-0.63]). ...For stage III melanoma, anti …
For stage III disease, recurrence risk is decreased with nivolumab (HR, 0.72 [95% CI, 0.60-0.86]), pembrolizumab (HR, 0.61 [95% CI, 0.51-0.7 …
Cutaneous Side Effects of BRAF Inhibitors in Advanced Melanoma: Review of the Literature.
Gençler B, Gönül M. Gençler B, et al. Dermatol Res Pract. 2016;2016:5361569. doi: 10.1155/2016/5361569. Epub 2016 Mar 3. Dermatol Res Pract. 2016. PMID: 27042173 Free PMC article. Review.
However, some adverse reactions have been reported in patients in the course of treatment. Cutaneous side effects are the most common adverse events among them with a broad spectrum. Both the case reports and several original clinical trials reported …
However, some adverse reactions have been reported in patients in the course of treatment. Cutaneous side effects are t …
Cutaneous adverse effects of targeted therapies: Part II: Inhibitors of intracellular molecular signaling pathways.
Macdonald JB, Macdonald B, Golitz LE, LoRusso P, Sekulic A. Macdonald JB, et al. J Am Acad Dermatol. 2015 Feb;72(2):221-36; quiz 237-8. doi: 10.1016/j.jaad.2014.07.033. J Am Acad Dermatol. 2015. PMID: 25592339 Review.
Along with skin cancer, deregulation of the PI3K-AKT-mTOR and RAS-RAF-MEK-ERK intracellular signaling pathways contributes to tumorigenesis of a multitude of other cancers, and inhibitors of these pathways are being actively studied. Similar to other classes of targeted th …
Along with skin cancer, deregulation of the PI3K-AKT-mTOR and RAS-RAF-MEK-ERK intracellular signaling pathways contributes to tumorigenesis …
Improved overall survival in melanoma with combined dabrafenib and trametinib.
Robert C, Karaszewska B, Schachter J, Rutkowski P, Mackiewicz A, Stroiakovski D, Lichinitser M, Dummer R, Grange F, Mortier L, Chiarion-Sileni V, Drucis K, Krajsova I, Hauschild A, Lorigan P, Wolter P, Long GV, Flaherty K, Nathan P, Ribas A, Martin AM, Sun P, Crist W, Legos J, Rubin SD, Little SM, Schadendorf D. Robert C, et al. N Engl J Med. 2015 Jan 1;372(1):30-9. doi: 10.1056/NEJMoa1412690. Epub 2014 Nov 16. N Engl J Med. 2015. PMID: 25399551 Free article. Clinical Trial.
BACKGROUND: The BRAF inhibitors vemurafenib and dabrafenib have shown efficacy as monotherapies in patients with previously untreated metastatic melanoma with BRAF V600E or V600K mutations. ...The objective response rate was 64% in the combination-therapy gro …
BACKGROUND: The BRAF inhibitors vemurafenib and dabrafenib have shown efficacy as monotherapies in patients with previously un …
Cutaneous adverse events to type I BRAF inhibitors: an analysis of effects associated with each inhibitor and therapeutic time interval to onset.
Filitis DC, Mahalingam M. Filitis DC, et al. Am J Clin Dermatol. 2013 Dec;14(6):461-71. doi: 10.1007/s40257-013-0045-5. Am J Clin Dermatol. 2013. PMID: 24048637 Review.
However, cutaneous adverse effects-from proliferative processes to more classic drug side effects-are increasingly being reported in patients on BRAF inhibitors. In this comprehensive literature review we provide (1) an all-inclusive list …
However, cutaneous adverse effects-from proliferative processes to more classic drug side effects-are increasing …
Adjuvant Dabrafenib plus Trametinib in Stage III BRAF-Mutated Melanoma.
Long GV, Hauschild A, Santinami M, Atkinson V, Mandalà M, Chiarion-Sileni V, Larkin J, Nyakas M, Dutriaux C, Haydon A, Robert C, Mortier L, Schachter J, Schadendorf D, Lesimple T, Plummer R, Ji R, Zhang P, Mookerjee B, Legos J, Kefford R, Dummer R, Kirkwood JM. Long GV, et al. N Engl J Med. 2017 Nov 9;377(19):1813-1823. doi: 10.1056/NEJMoa1708539. Epub 2017 Sep 10. N Engl J Med. 2017. PMID: 28891408 Free article. Clinical Trial.
BACKGROUND: Combination therapy with the BRAF inhibitor dabrafenib plus the MEK inhibitor trametinib improved survival in patients with advanced melanoma with BRAF V600 mutations. ...CONCLUSIONS: Adjuvant use of combination therapy with dabrafenib plus …
BACKGROUND: Combination therapy with the BRAF inhibitor dabrafenib plus the MEK inhibitor trametinib improved survival …
355 results