Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/10211
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dc.contributor.authorZugazagoitia, Jon-
dc.contributor.authorPonce, Santiago-
dc.contributor.authorFerrer, Irene-
dc.contributor.authorPinelo, Sonia Molina-
dc.contributor.authorAres, Luis Paz-
dc.contributor.authorDuque, Cristiano Guedes-
dc.date.accessioned2022-08-17T18:59:12Z-
dc.date.available2022-08-17T18:59:12Z-
dc.date.issued2016-
dc.identifier.citationZUGAZAGOITIA, Jon et al. Current challenges in cancer treatment. Clinical Therapeutics, v. 38, n. 7, p. 1551-1566, 2016.-
dc.identifier.issn0149-2918-
dc.identifier.urihttp://sr-vmlxaph03:8080/jspui/handle/123456789/10211-
dc.descriptionp. 1551-1566.: tab. p&b.-
dc.description.abstractIn 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.-
dc.publisherClinical Therapeuticspt_BR
dc.subjectSegunda Neoplasia Primáriapt_BR
dc.subjectNeoplasms Second Primarypt_BR
dc.subjectInibidores de Checkpoint Imunológicopt_BR
dc.subjectImmune Checkpoint Inhibitorspt_BR
dc.subjectDesenvolvimento de Medicamentospt_BR
dc.subjectDrug Developmentpt_BR
dc.subjectImunoterapiapt_BR
dc.subjectImmunotherapypt_BR
dc.subjectNeoplasias Pulmonarespt_BR
dc.subjectLung Neoplasmspt_BR
dc.subjectSequenciamento de Nucleotídeos em Larga Escalapt_BR
dc.subjectHigh-Throughput Nucleotide Sequencingpt_BR
dc.subjectMedicina de Precisãopt_BR
dc.subjectPrecision Medicinept_BR
dc.subjectTerapia de Alvo Molecularpt_BR
dc.subjectMolecular Targeted Therapypt_BR
dc.titleCurrent challenges in cancer treatmentpt_BR
dc.TypeArticlept_BR
Appears in Collections:Artigos de Periódicos da área de Oncologia Clínica

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