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A Social Network Analysis of Treatment Discoveries in Cancer

Controlled clinical trials are widely considered to be the vehicle to treatment discovery in cancer that leads to significant improvements in health outcomes including an increase in life expectancy. We have previously shown that the pattern of therapeutic discovery in randomized controlled trials (...

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Autores principales: Tsalatsanis, Athanasios, Barnes, Laura, Hozo, Iztok, Skvoretz, John, Djulbegovic, Benjamin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065482/
https://www.ncbi.nlm.nih.gov/pubmed/21464896
http://dx.doi.org/10.1371/journal.pone.0018060
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author Tsalatsanis, Athanasios
Barnes, Laura
Hozo, Iztok
Skvoretz, John
Djulbegovic, Benjamin
author_facet Tsalatsanis, Athanasios
Barnes, Laura
Hozo, Iztok
Skvoretz, John
Djulbegovic, Benjamin
author_sort Tsalatsanis, Athanasios
collection PubMed
description Controlled clinical trials are widely considered to be the vehicle to treatment discovery in cancer that leads to significant improvements in health outcomes including an increase in life expectancy. We have previously shown that the pattern of therapeutic discovery in randomized controlled trials (RCTs) can be described by a power law distribution. However, the mechanism generating this pattern is unknown. Here, we propose an explanation in terms of the social relations between researchers in RCTs. We use social network analysis to study the impact of interactions between RCTs on treatment success. Our dataset consists of 280 phase III RCTs conducted by the NCI from 1955 to 2006. The RCT networks are formed through trial interactions formed i) at random, ii) based on common characteristics, or iii) based on treatment success. We analyze treatment success in terms of survival hazard ratio as a function of the network structures. Our results show that the discovery process displays power law if there are preferential interactions between trials that may stem from researchers' tendency to interact selectively with established and successful peers. Furthermore, the RCT networks are “small worlds”: trials are connected through a small number of ties, yet there is much clustering among subsets of trials. We also find that treatment success (improved survival) is proportional to the network centrality measures of closeness and betweenness. Negative correlation exists between survival and the extent to which trials operate within a limited scope of information. Finally, the trials testing curative treatments in solid tumors showed the highest centrality and the most influential group was the ECOG. We conclude that the chances of discovering life-saving treatments are directly related to the richness of social interactions between researchers inherent in a preferential interaction model.
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spelling pubmed-30654822011-04-04 A Social Network Analysis of Treatment Discoveries in Cancer Tsalatsanis, Athanasios Barnes, Laura Hozo, Iztok Skvoretz, John Djulbegovic, Benjamin PLoS One Research Article Controlled clinical trials are widely considered to be the vehicle to treatment discovery in cancer that leads to significant improvements in health outcomes including an increase in life expectancy. We have previously shown that the pattern of therapeutic discovery in randomized controlled trials (RCTs) can be described by a power law distribution. However, the mechanism generating this pattern is unknown. Here, we propose an explanation in terms of the social relations between researchers in RCTs. We use social network analysis to study the impact of interactions between RCTs on treatment success. Our dataset consists of 280 phase III RCTs conducted by the NCI from 1955 to 2006. The RCT networks are formed through trial interactions formed i) at random, ii) based on common characteristics, or iii) based on treatment success. We analyze treatment success in terms of survival hazard ratio as a function of the network structures. Our results show that the discovery process displays power law if there are preferential interactions between trials that may stem from researchers' tendency to interact selectively with established and successful peers. Furthermore, the RCT networks are “small worlds”: trials are connected through a small number of ties, yet there is much clustering among subsets of trials. We also find that treatment success (improved survival) is proportional to the network centrality measures of closeness and betweenness. Negative correlation exists between survival and the extent to which trials operate within a limited scope of information. Finally, the trials testing curative treatments in solid tumors showed the highest centrality and the most influential group was the ECOG. We conclude that the chances of discovering life-saving treatments are directly related to the richness of social interactions between researchers inherent in a preferential interaction model. Public Library of Science 2011-03-28 /pmc/articles/PMC3065482/ /pubmed/21464896 http://dx.doi.org/10.1371/journal.pone.0018060 Text en Tsalatsanis et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tsalatsanis, Athanasios
Barnes, Laura
Hozo, Iztok
Skvoretz, John
Djulbegovic, Benjamin
A Social Network Analysis of Treatment Discoveries in Cancer
title A Social Network Analysis of Treatment Discoveries in Cancer
title_full A Social Network Analysis of Treatment Discoveries in Cancer
title_fullStr A Social Network Analysis of Treatment Discoveries in Cancer
title_full_unstemmed A Social Network Analysis of Treatment Discoveries in Cancer
title_short A Social Network Analysis of Treatment Discoveries in Cancer
title_sort social network analysis of treatment discoveries in cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065482/
https://www.ncbi.nlm.nih.gov/pubmed/21464896
http://dx.doi.org/10.1371/journal.pone.0018060
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