Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date

The disease course of BRAF (v-raf murine sarcoma viral oncogene homolog B1)-mutant melanoma has been drastically improved by the arrival of targeted therapies. NRAS (neuroblastoma RAS viral oncogene homolog)-mutated melanoma represents 15–25% of all metastatic melanoma patients. It currently does no...

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Main Authors: Amélie Boespflug, Julie Caramel, Stephane Dalle, Luc Thomas
Format: Article
Language:English
Published: SAGE Publishing 2017-07-01
Series:Therapeutic Advances in Medical Oncology
Online Access:https://doi.org/10.1177/1758834017708160
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spelling doaj-e1d4ea48b2fd46d1a7d1cff506bc82152020-11-25T03:34:45ZengSAGE PublishingTherapeutic Advances in Medical Oncology1758-83401758-83592017-07-01910.1177/1758834017708160Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to dateAmélie BoespflugJulie CaramelStephane DalleLuc ThomasThe disease course of BRAF (v-raf murine sarcoma viral oncogene homolog B1)-mutant melanoma has been drastically improved by the arrival of targeted therapies. NRAS (neuroblastoma RAS viral oncogene homolog)-mutated melanoma represents 15–25% of all metastatic melanoma patients. It currently does not have an approved targeted therapy. Metastatic patients receive immune-based therapies as first-line treatments, then cytotoxic chemotherapy like carboplatin/paclitaxel (C/P), dacarbazine (DTIC) or temozolomide (TMZ) as a second-line treatment. We will review current preclinical and clinical developments in NRAS -mutated melanoma, and analyze ongoing clinical trials that are evaluating the benefit of different targeted and immune-based therapies, either tested as single agents or in combination, in NRAS -mutant melanoma.https://doi.org/10.1177/1758834017708160
collection DOAJ
language English
format Article
sources DOAJ
author Amélie Boespflug
Julie Caramel
Stephane Dalle
Luc Thomas
spellingShingle Amélie Boespflug
Julie Caramel
Stephane Dalle
Luc Thomas
Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
Therapeutic Advances in Medical Oncology
author_facet Amélie Boespflug
Julie Caramel
Stephane Dalle
Luc Thomas
author_sort Amélie Boespflug
title Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
title_short Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
title_full Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
title_fullStr Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
title_full_unstemmed Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
title_sort treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date
publisher SAGE Publishing
series Therapeutic Advances in Medical Oncology
issn 1758-8340
1758-8359
publishDate 2017-07-01
description The disease course of BRAF (v-raf murine sarcoma viral oncogene homolog B1)-mutant melanoma has been drastically improved by the arrival of targeted therapies. NRAS (neuroblastoma RAS viral oncogene homolog)-mutated melanoma represents 15–25% of all metastatic melanoma patients. It currently does not have an approved targeted therapy. Metastatic patients receive immune-based therapies as first-line treatments, then cytotoxic chemotherapy like carboplatin/paclitaxel (C/P), dacarbazine (DTIC) or temozolomide (TMZ) as a second-line treatment. We will review current preclinical and clinical developments in NRAS -mutated melanoma, and analyze ongoing clinical trials that are evaluating the benefit of different targeted and immune-based therapies, either tested as single agents or in combination, in NRAS -mutant melanoma.
url https://doi.org/10.1177/1758834017708160
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