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Personalized Medicine in Malignant Melanoma: Towards Patient Tailored Treatment
- Source :
- Frontiers in Oncology, Frontiers in Oncology, Vol 8 (2018)
- Publication Year :
- 2018
- Publisher :
- Frontiers Media S.A., 2018.
-
Abstract
- Despite enormous international efforts, skin melanoma is still a major clinical challenge. Melanoma takes a top place among the most common cancer types and it has one of the most rapidly increasing incidences in many countries around the world. Until recent years, there have been limited options for effective systemic treatment of disseminated melanoma. However, lately, we have experienced a rapid advancement in the understanding of the biology and molecular background of the disease. This has led to new molecular classifications and the development of more effective targeted therapies adapted to distinct melanoma subtypes. Not only are these treatments more effective but they can be rationally prescribed to the patients standing to benefit. As such, melanoma management has now become one of the most developed for personalized medicine. The aim of the present paper is to summarize the current knowledge on melanoma molecular classification, predictive markers, combination therapies, as well as emerging new treatments.
- Subjects :
- 0301 basic medicine
Cancer Research
medicine.medical_specialty
medicine.medical_treatment
Disease
Review
ubiquitination
lcsh:RC254-282
Targeted therapy
03 medical and health sciences
0302 clinical medicine
Molecular classification
medicine
melanoma
Intensive care medicine
receptor tyrosine kinases
business.industry
Melanoma
Cancer
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
medicine.disease
Tailored treatment
targeted therapy
030104 developmental biology
Oncology
030220 oncology & carcinogenesis
Personalized medicine
functional selectivity
Skin melanoma
business
signaling
Subjects
Details
- Language :
- English
- ISSN :
- 2234943X
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Frontiers in Oncology
- Accession number :
- edsair.doi.dedup.....9764482a8cfd90ee78e1984fd4bd69d8