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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Series: | Therapeutic Advances in Medical Oncology |
Online Access: | https://doi.org/10.1177/1758834017708160 |
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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 |
work_keys_str_mv |
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