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Seven decades of chemotherapy clinical trials: a pan-cancer social network analysis

Authors :
Candice Schwartz
Qingxia Chen
Jess Behrens
Seema Nagpal
Shervin A. Etemad
Benjamin F. Tillman
Ronald S. Go
Kristin Wuichet
Elizabeth Sigworth
Xuanyi Li
John P. Greer
Travis J. Osterman
Ivy Abraham
Summer B. Dewdney
Andrew J. Cowan
Andrew Malty
Samuel M. Rubinstein
Neeta K. Venepalli
Jeremy L. Warner
Adrianne H. Wu
Peter C. Yang
Sanjai Sharma
Hermina D Fernandes
Eddy J. Chen
Matthew J. Rioth
Elizabeth I. Buchbinder
Rozina A. Chowdhery
Ari Seifter
Edward P. Ambinder
Martin W. Schoen
Sanjay R. Mohan
Naina Singh
Michael K. Gibson
Source :
Scientific Reports, Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Publication Year :
2020

Abstract

BackgroundClinical trials establish the standard of care for cancer and other diseases. While social network analysis has been applied to basic sciences, the social component of clinical trial research is not well characterized. We examined the social network of cancer clinical trialists and its dynamic development over more than 70 years, including the roles of subspecialization and gender in relation to traditional and network-based metrics of productivity.MethodsWe conducted a social network analysis of authors publishing chemotherapy-based prospective trials from 1946-2018, based on the curated knowledge base HemOnc.org, examining: 1) network density; 2) modularity; 3) assortativity; 4) betweenness centrality; 5) PageRank; and 6) the proportion of co-authors sharing the same primary cancer subspecialty designation. Individual author impact and productive period were analyzed as a function of gender and subspecialty.FindingsFrom 1946-2018, the network grew to 29,197 authors and 697,084 co-authors. While 99.4% of authors were directly or indirectly connected as of 2018, the network had very few connections and was very siloed by cancer subspecialty. Small numbers of individuals were highly connected and had disproportionate impact (scale-free effects). Women were under-represented and likelier to have lower impact, shorter productive periods (PInterpretationThe network of cancer clinical trialists is best characterized as a strategic or “mixed-motive” network, with cooperative and competitive elements influencing its appearance.Network effects e.g., low centrality, which may limit access to high-profile individuals, likely contribute to ongoing disparities.FundingVanderbilt Initiative for Interdisciplinary Research; National Institutes of Health; National Science FoundationResearch in contextEvidence before this studyWe reviewed the literature on social networks from the 1800’s to 2018. Additionally, MEDLINE was searched for (“Social Networking”[Mesh] OR “Social Network Analysis”) AND (“Clinical Trials as Topic”[Mesh] OR “Hematology”[Mesh] OR “Medical Oncology”[Mesh]) without date restriction. The MEDLINE search yielded 43 results, of which 8 were relevant; none considered gender nor temporality in their analyses. To our knowledge, there has not been any similar study of the dynamic social network of clinical trialists from the inception of the fields of medical oncology and hematology to the present.Added value of this studyThis is the first dynamic social network analysis of cancer clinical trialists. We found that the network was sparse and siloed with a small number of authors having disproportionate impact and influence as measured by network metrics such as PageRank; these metrics have become more disproportionate over time. Women were under-represented and likelier to have lower impact, shorter productive periods, less network centrality, and a greater proportion of co-authors in their same cancer subspecialty.Implications of all the available evidenceWhile gender disparities have been demonstrated in many fields including hematology/oncology, our analysis is the first to show that network factors themselves are significantly implicated in gender disparity. The increasing coalescence of the network by traditional cancer type and around a small number of high-impact individuals implies challenges when the field pivots from traditionally disease-oriented subspecialties to a precision oncology paradigm. New mechanisms are needed to ensure diversity of clinical trialists.

Details

ISSN :
20452322 and 19462018
Volume :
10
Issue :
1
Database :
OpenAIRE
Journal :
Scientific reports
Accession number :
edsair.doi.dedup.....b2ccdf721284ca5c95d6c73578731e11