Author:
Berlow Noah E.,Rikhi Rikhi,Geltzeiler Mathew N.,Abraham Jinu,Svalina Matthew N.,Davis Lara E.,Wise Erin,Mancini Maria,Noujaim Jonathan,Mansoor Atiya,Quist Michael J.,Matlock Kevin L.,Goros Martin W.,Hernandez Brian S.,Doung Yee C.,Thway Khin,Tsukahara Tomohide,Nishio Jun,Huang Elaine C. Huang,Airhart Susan,Bult Carol J.,Gandour-Edwards Regina,Maki Robert G.,Jones Robin L.,Michalek Joel E.,Milovancev Milan,Ghosh Souparno,Pal Ranadip,Keller Charles
Abstract
ABSTRACTCancer patients with advanced disease exhaust available clinical regimens and lack actionable genomic medicine results, leaving a large patient population without effective treatments options when their disease inevitably progresses. To address the unmet clinical need for evidence-based therapy assignment when standard clinical approaches have failed, we have developed a probabilistic computational modeling approach which integrates sequencing data with functional assay data to develop patient-specific combination cancer treatments. This computational modeling approach addresses three major challenges in personalized cancer therapy, which we validate across multiple species via computationally-designed personalized synergistic drug combination predictions, identification of unifying therapeutic targets to overcome intra-tumor heterogeneity, and mitigation of cancer cell resistance and rewiring mechanisms. These proof-of-concept studies support the use of an integrative functional approach to personalized combination therapy prediction for the population of high-risk cancer patients lacking viable clinical options and without actionable DNA sequencing-based therapy.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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