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Heuristic value-based framework for lung cancer decision-making
Heuristics and the application of fast-and-frugal trees may play a role in establishing a clinical decision-making framework for value-based oncology. We determined whether clinical decision-making in oncology can be structured heuristically based on the timeline of the patient's treatment, cli...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057456/ https://www.ncbi.nlm.nih.gov/pubmed/30042820 http://dx.doi.org/10.18632/oncotarget.25643 |
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author | Mambetsariev, Isa Pharaon, Rebecca Nam, Arin Knopf, Kevin Djulbegovic, Benjamin Villaflor, Victoria M. Vokes, Everett E. Salgia, Ravi |
author_facet | Mambetsariev, Isa Pharaon, Rebecca Nam, Arin Knopf, Kevin Djulbegovic, Benjamin Villaflor, Victoria M. Vokes, Everett E. Salgia, Ravi |
author_sort | Mambetsariev, Isa |
collection | PubMed |
description | Heuristics and the application of fast-and-frugal trees may play a role in establishing a clinical decision-making framework for value-based oncology. We determined whether clinical decision-making in oncology can be structured heuristically based on the timeline of the patient's treatment, clinical intuition, and evidence-based medicine. A group of 20 patients with advanced non-small cell lung cancer (NSCLC) were enrolled into the study for extensive treatment analysis and sequential decision-making. The extensive clinical and genomic data allowed us to evaluate the methodology and efficacy of fast-and-frugal trees as a way to quantify clinical decision-making. The results of the small cohort will be used to further advance the heuristic framework as a way of evaluating a large number of patients within registries. Among the cohort whose data was analyzed, substitution and amplification mutations occurred most frequently. The top five most prevalent genomic alterations were TP53 (45%), ALK (40%), LRP1B (30%), CDKN2A (25%), and MYC (25%). These 20 cases were analyzed by this clinical decision-making process and separated into two distinctions: 10 straightforward cases that represented a clearer decision-making path and 10 complex cases that represented a more intricate treatment pathway. The myriad of information from each case and their distinct pathways was applied to create the foundation of a framework for lung cancer decision-making as an aid for oncologists. In late-stage lung cancer patients, the fast-and-frugal heuristics can be utilized as a strategy of quantifying proper decision-making with limited information. |
format | Online Article Text |
id | pubmed-6057456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-60574562018-07-24 Heuristic value-based framework for lung cancer decision-making Mambetsariev, Isa Pharaon, Rebecca Nam, Arin Knopf, Kevin Djulbegovic, Benjamin Villaflor, Victoria M. Vokes, Everett E. Salgia, Ravi Oncotarget Research Paper Heuristics and the application of fast-and-frugal trees may play a role in establishing a clinical decision-making framework for value-based oncology. We determined whether clinical decision-making in oncology can be structured heuristically based on the timeline of the patient's treatment, clinical intuition, and evidence-based medicine. A group of 20 patients with advanced non-small cell lung cancer (NSCLC) were enrolled into the study for extensive treatment analysis and sequential decision-making. The extensive clinical and genomic data allowed us to evaluate the methodology and efficacy of fast-and-frugal trees as a way to quantify clinical decision-making. The results of the small cohort will be used to further advance the heuristic framework as a way of evaluating a large number of patients within registries. Among the cohort whose data was analyzed, substitution and amplification mutations occurred most frequently. The top five most prevalent genomic alterations were TP53 (45%), ALK (40%), LRP1B (30%), CDKN2A (25%), and MYC (25%). These 20 cases were analyzed by this clinical decision-making process and separated into two distinctions: 10 straightforward cases that represented a clearer decision-making path and 10 complex cases that represented a more intricate treatment pathway. The myriad of information from each case and their distinct pathways was applied to create the foundation of a framework for lung cancer decision-making as an aid for oncologists. In late-stage lung cancer patients, the fast-and-frugal heuristics can be utilized as a strategy of quantifying proper decision-making with limited information. Impact Journals LLC 2018-07-06 /pmc/articles/PMC6057456/ /pubmed/30042820 http://dx.doi.org/10.18632/oncotarget.25643 Text en Copyright: © 2018 Mambetsariev et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Mambetsariev, Isa Pharaon, Rebecca Nam, Arin Knopf, Kevin Djulbegovic, Benjamin Villaflor, Victoria M. Vokes, Everett E. Salgia, Ravi Heuristic value-based framework for lung cancer decision-making |
title | Heuristic value-based framework for lung cancer decision-making |
title_full | Heuristic value-based framework for lung cancer decision-making |
title_fullStr | Heuristic value-based framework for lung cancer decision-making |
title_full_unstemmed | Heuristic value-based framework for lung cancer decision-making |
title_short | Heuristic value-based framework for lung cancer decision-making |
title_sort | heuristic value-based framework for lung cancer decision-making |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057456/ https://www.ncbi.nlm.nih.gov/pubmed/30042820 http://dx.doi.org/10.18632/oncotarget.25643 |
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