Safety Profiles and Pharmacovigilance Considerations for Recently Patented Anticancer Drugs: Cutaneous Melanoma

Autor: Giulia Fornasier, Paolo Baldo, Maria Antonietta Pizzichetta, Debora Basile, Francesco Lo Re, C. Lisanti, Fabio Puglisi, Giuseppe Corona
Přispěvatelé: Pizzichetta, Maria A, Basile, Debora, Lisanti, Camilla, Baldo, Paolo, Fornasier, Giulia, Lo Re, Francesco, Corona, Giuseppe, Puglisi, Fabio
Rok vydání: 2018
Předmět:
advanced melanoma
Cancer Research
Skin Neoplasms
medicine.medical_treatment
Targeted therapy
Pharmacovigilance
0302 clinical medicine
Antineoplastic Agents
Immunological

Drug Discovery
Pharmacology (medical)
030212 general & internal medicine
Molecular Targeted Therapy
Neoplasm Metastasis
Drug Approval
Melanoma
adverse drug reactions
Clinical Trials as Topic
Antibodies
Monoclonal

General Medicine
targeted therapy
side effects
Oncology
030220 oncology & carcinogenesis
immunotherapy
drug-related toxicity
Proto-Oncogene Proteins B-raf
medicine.medical_specialty
side effect
adverse drug reaction
Antineoplastic Agents
Patents as Topic
03 medical and health sciences
medicine
Humans
Target therapy
Intensive care medicine
Protein Kinase Inhibitors
Advanced melanoma
business.industry
Adjuvant melanoma
pharmacovigilance
Immunotherapy
medicine.disease
Cutaneous melanoma
Skin cancer
business
Zdroj: Recent patents on anti-cancer drug discovery. 14(3)
ISSN: 2212-3970
Popis: Background:Malignant melanoma is a skin cancer responsible for 90% of cutaneous cancer- related deaths. In recent years, breakthroughs in treatment strategy have revolutionized the prognosis in both early and advanced melanoma patients. In particular, treatment with monoclonal antibodies targeting co-inhibitory checkpoints or specific molecular pathways leads to a new era of promising options, by prolonging the survival time of these patients.:Moreover, unlike the chemotherapy that was used until some time ago, these new drugs have a good and more manageable toxicity profile. However, because of the recent introduction in clinical practice of the new agents, there is a learning curve among physicians regarding early recognition and management of the associated side effects.Objective:The analysis of the toxicity profiles of the different agents currently studied for the treatment of early and advanced melanoma, and the description of several relevant recent patents in this field, are the aims of this review.Methods:This is a systematically conducted review based on current clinical guidelines and on international Pharmacovigilance databases (AERS-Eudravigilance - WHO Vigibase).Results:Our systematic analysis outlines a comprehensive overview of the pharmacology, clinical application and the safety of recent anticancer drugs to treat melanoma, which can be an essential instrument for health professionals and researchers.Conclusion:The new oncological therapies against melanoma are based on increasingly specific biological and immunological targets. For this reason, the potential toxicities that are expected from patients would be less relevant than the systemic "classical" chemotherapy. However, the new therapies are not free from the risk of causing adverse reactions, some of which must be managed promptly and appropriately; moreover, the multiplicity of the metabolic pathways exposes the new target therapies to relevant potential interactions. This review can help to understand how important it is not to underestimate potential adverse drug reactions related to new targeted therapies.
Databáze: OpenAIRE