Abstract B016: Unravelling personalized drug vulnerabilities in pediatric solid tumors—functional precision medicine approach

Abstract Many pediatric cancer patients with high-risk primary, refractory, or relapsed tumors still lack effective treatment strategies and frequently suffer from both acute and delayed adverse drug effects, including secondary cancers. These tumors are generally characterized by very few druggable molecular alterations, diminishing the advantage of genetics in defining patient-specific treatments. The purpose of this study is to utilize the functional precision medicine approach to provide improved diagnostics and better therapy options for pediatric solid tumors through deep molecular and functional profiling in a patient-specific manner. Here, we describe the results of our current study, which includes exome sequencing for germline and somatic mutations, and transcriptomics analysis for fusion genes, as well as ex vivo drug testing of patient-derived cancer cells (PDCs) in real-time clinical set-up. Our current clinical data and sample collection, currently from 40 patients, include different types of pediatric solid tumors, such as central nervous system (CNS) tumors, sarcomas, and neuroblastomas. We have prepared PDC cultures and screened them using a 3D-drug sensitivity and resistance testing (DSRT) platform with an internationally defined pediatric solid tumor drug panel. Our results include the drug testing results of control cell lines and primary healthy cells to assess the general cytotoxicity of the drugs and patient-specific responses. We present our "fast-track" functional precision medicine concept, incorporated as part of biobank operations to return clinically relevant findings back to the treating clinicians, and exemplify the data returned to the clinics as well as its potential clinical impact. In conclusion, our findings demonstrate that the functional precision medicine approach can i) help to discover clinically relevant molecular events important for diagnosis and treatment, and ii) increase our biological understanding of drug vulnerabilities in pediatric cancers. Citation Format: Sara Kuusela, Enni Martikainen, Katja Eloranta, Wenyu Wang, Romika Kumari, Swapnil Potdar, Giovanna Dashi, Jouko Lohi, Aino Mutka, Olli Tynninen, Jukka Kanerva, Virve Pentikäinen, Minna Koskenvuo, Vilja M. Pietiäinen. Unravelling personalized drug vulnerabilities in pediatric solid tumors—functional precision medicine approach [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pediatric Cancer Research; 2024 Sep 5-8; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl):Abstract nr B016.

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Journal
Cancer Research
Published
2024-09-05
DOI
https://doi.org/10.1158/1538-7445.pediatric24-b016
Primary Topic
Cancer Genomics and Diagnostics
Type
article
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article

Abstract B016: Unravelling personalized drug vulnerabilities in pediatric solid tumors—functional precision medicine approach

M. Koskenvuo, Virve Pentikäinen, Giovanna Dashi, Olli Tynninen et al.
Cancer Research
Cancer Genomics and Diagnostics
article

Abstract B016: Unravelling personalized drug vulnerabilities in pediatric solid tumors—functional precision medicine approach

M. Koskenvuo, Virve Pentikäinen, Giovanna Dashi, Olli Tynninen, Romika Kumari, Katja Eloranta, Sara Kuusela, Jukka Kanerva, Swapnil Potdar, Aino Mutka, Vilja Pietiäinen, Wenyu Wang, Jouko Lohi, Enni Martikainen
article en

Abstract

Abstract Many pediatric cancer patients with high-risk primary, refractory, or relapsed tumors still lack effective treatment strategies and frequently suffer from both acute and delayed adverse drug effects, including secondary cancers. These tumors are generally characterized by very few druggable molecular alterations, diminishing the advantage of genetics in defining patient-specific treatments. The purpose of this study is to utilize the functional precision medicine approach to provide improved diagnostics and better therapy options for pediatric solid tumors through deep molecular and functional profiling in a patient-specific manner. Here, we describe the results of our current study, which includes exome sequencing for germline and somatic mutations, and transcriptomics analysis for fusion genes, as well as ex vivo drug testing of patient-derived cancer cells (PDCs) in real-time clinical set-up. Our current clinical data and sample collection, currently from 40 patients, include different types of pediatric solid tumors, such as central nervous system (CNS) tumors, sarcomas, and neuroblastomas. We have prepared PDC cultures and screened them using a 3D-drug sensitivity and resistance testing (DSRT) platform with an internationally defined pediatric solid tumor drug panel. Our results include the drug testing results of control cell lines and primary healthy cells to assess the general cytotoxicity of the drugs and patient-specific responses. We present our "fast-track" functional precision medicine concept, incorporated as part of biobank operations to return clinically relevant findings back to the treating clinicians, and exemplify the data returned to the clinics as well as its potential clinical impact. In conclusion, our findings demonstrate that the functional precision medicine approach can i) help to discover clinically relevant molecular events important for diagnosis and treatment, and ii) increase our biological understanding of drug vulnerabilities in pediatric cancers. Citation Format: Sara Kuusela, Enni Martikainen, Katja Eloranta, Wenyu Wang, Romika Kumari, Swapnil Potdar, Giovanna Dashi, Jouko Lohi, Aino Mutka, Olli Tynninen, Jukka Kanerva, Virve Pentikäinen, Minna Koskenvuo, Vilja M. Pietiäinen. Unravelling personalized drug vulnerabilities in pediatric solid tumors—functional precision medicine approach [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pediatric Cancer Research; 2024 Sep 5-8; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl):Abstract nr B016.

Cancer ResearchVol. 84(17_Supplement)
University of Helsinki (FI), Helsinki University Hospital (FI), Institute for Molecular Medicine Finland (FI)
Openalex Percentile: Top 78%
Cancer Genomics and Diagnostics
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