First-line treatment of NRAS-mutated metastatic melanoma with a MEK inhibitor.
Aged, 80 and over
Azetidines
/ therapeutic use
GTP Phosphohydrolases
/ genetics
Humans
Male
Melanoma
/ drug therapy
Membrane Proteins
/ genetics
Mitogen-Activated Protein Kinase Kinases
/ antagonists & inhibitors
Mutation
Neoplasm Metastasis
Piperidines
/ therapeutic use
Skin Neoplasms
/ drug therapy
Treatment Outcome
BRAF wild type
MEK inhibitor
NRAS mutation
metastatic melanoma
Journal
Journal of cancer research and therapeutics
ISSN: 1998-4138
Titre abrégé: J Cancer Res Ther
Pays: India
ID NLM: 101249598
Informations de publication
Date de publication:
Historique:
entrez:
16
3
2021
pubmed:
17
3
2021
medline:
20
11
2021
Statut:
ppublish
Résumé
Until recently, standard treatment for advanced melanoma comprised basically dacarbazine and interleukin-2, leading to low response rates and significant toxicity. These days, new treatments such as immunotherapy (anti-CTLA4 and anti-PD1 antibodies) and targeted therapy with BRAF/MEK-inhibitor combinations for patients harboring a BRAF mutation are available. In BRAF wild-type patients harboring an NRAS mutation, not fit for immunotherapy treatment options are still dismal. We describe an 84-year-old patient with widespread metastatic melanoma. He presented in July 2015 with a cerebral hemorrhage under anticoagulation for atrial fibrillation. Computed tomography revealed extensive metastatic disease (liver, lung, bones, lymph nodes, heart, and brain). Molecular testing was negative for BRAF but showed the presence of an NRAS mutation in exon 3 (pQ61K [c.181C>A]). The patient received as first-line treatment two cycles of cobimetinib showing a good partial remission and manageable side effects.
Identifiants
pubmed: 33723170
pii: JCanResTher_2021_17_1_276_264222
doi: 10.4103/jcrt.JCRT_50_18
doi:
Substances chimiques
Azetidines
0
Membrane Proteins
0
Piperidines
0
Mitogen-Activated Protein Kinase Kinases
EC 2.7.12.2
GTP Phosphohydrolases
EC 3.6.1.-
NRAS protein, human
EC 3.6.1.-
cobimetinib
ER29L26N1X
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
276-278Déclaration de conflit d'intérêts
None