Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/10211
Title: Current challenges in cancer treatment
Authors: Zugazagoitia, Jon
Ponce, Santiago
Ferrer, Irene
Pinelo, Sonia Molina
Ares, Luis Paz
Duque, Cristiano Guedes
Keywords: Segunda Neoplasia Primária
Neoplasms Second Primary
Inibidores de Checkpoint Imunológico
Immune Checkpoint Inhibitors
Desenvolvimento de Medicamentos
Drug Development
Imunoterapia
Immunotherapy
Neoplasias Pulmonares
Lung Neoplasms
Sequenciamento de Nucleotídeos em Larga Escala
High-Throughput Nucleotide Sequencing
Medicina de Precisão
Precision Medicine
Terapia de Alvo Molecular
Molecular Targeted Therapy
Issue Date: 2016
Publisher: Clinical Therapeutics
Citation: ZUGAZAGOITIA, Jon et al. Current challenges in cancer treatment. Clinical Therapeutics, v. 38, n. 7, p. 1551-1566, 2016.
Abstract: In this review, we highlight the current concepts and discuss some of the current challenges and future prospects in cancer therapy. We frequently use the example of lung cancer. Methods: We conducted a nonsystematic PubMed search, selecting the most comprehensive and relevant research articles, clinical trials, translational papers, and review articles on precision oncology and immuno oncology. Papers were prioritized and selected based on their originality and potential clinical applicability. Findings: Two major revolutions have changed cancer treatment paradigms in the past few years: targeting actionable alterations in oncogene-driven cancers and immuno-oncology. Important challenges are still ongoing in both fields of cancer therapy. On the one hand, druggable genomic alterations are diverse and represent only small subsets of patients in certain tumor types, which limits testing their clinical impact in biomarker-driven clinical trials. Next-generation sequencing technologies are increas ingly being implemented for molecular prescreening in clinical research, but issues regarding clinical interpre tation of large genomic data make their wide clinical use difficult. Further, dealing with tumor heterogene ity and acquired resistance is probably the main limitation for the success of precision oncology. On the other hand, long-term survival benefits with immune checkpoint inhibitors (anti programmed death cell protein-1/programmed death cell ligand-1 [PD-1/L1] and anti cytotoxic T lymphocyte antigen-4 monoclonal antibodies) are restricted to a minority of patients, and no predictive markers are yet robustly validated that could help us recognize these subsets and optimize treatment delivery and selection. To achieve long-term survival benefits, drug combina tions targeting several molecular alterations or cancer hallmarks might be needed. This will probably be one of the most challenging but promising precision cancer treatment strategies in the future. Implications: Targeting single molecular abnormal ities or cancer pathways has achieved good clinical responses that have modestly affected survival in some cancers. However, this approach to cancer treatment is still reductionist, and many challenges need to be met to improve treatment outcomes with our patients. (Clin Ther. 2016;38:1551–1566) & 2016 Elsevier HS Journals, Inc. All rights reserved.
Description: p. 1551-1566.: tab. p&b.
URI: http://sr-vmlxaph03:8080/jspui/handle/123456789/10211
ISSN: 0149-2918
Appears in Collections:Artigos de Periódicos da área de Oncologia Clínica

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