Real-World Performance of Integrative Clinical Genomics in Pediatric Precision Oncology

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Publikace nespadá pod Fakultu sociálních studií, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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POKORNÁ Petra PÁLOVÁ Hana ADAMCOVÁ Soňa JUGAS Robin AL TUKMACHI Dagmar KÝR Michal KNOFLÍČKOVÁ Dana KOŽELKOVÁ Kateřina BYSTRÝ Vojtěch MEJSTŘÍKOVÁ Soňa MERTA Tomáš TRACHTOVÁ Karolína HLOUŠKOVÁ Eliška MÚDRY Peter PAVELKA Zdeněk BAJČIOVÁ Viera TINKA Pavel JAROŠOVÁ Marie CATELA IVKOVIĆ Tina MADLENER Sibylle PÁL Karol STEPIEN Natalia MAYR Lisa TICHÝ Boris NOVÁKOVÁ Klára JEŽOVÁ Marta KOZÁKOVÁ Šárka VAŇÁČKOVÁ Jitka RADOVÁ Lenka STEININGER Karin HABERLER Christine GOJO Johannes ŠTĚRBA Jaroslav SLABÝ Ondřej

Rok publikování 2024
Druh Článek v odborném periodiku
Časopis / Zdroj Laboratory Investigation
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://www.sciencedirect.com/science/article/pii/S0023683724018397?via%3Dihub
Doi http://dx.doi.org/10.1016/j.labinv.2024.102161
Klíčová slova next-generation sequencing; pediatric oncology; precision medicine
Přiložené soubory
Popis Despite significant improvement in the survival of pediatric patients with cancer, treatment outcomes for high-risk, relapsed, and refractory cancers remain unsatisfactory. Moreover, prolonged survival is frequently associated with long-term adverse effects due to intensive multimodal treatments. Accelerating the progress of pediatric oncology requires both therapeutic advances and strategies to mitigate the long-term cytotoxic side effects, potentially through targeting specific molecular drivers of pediatric malignancies. In this report, we present the results of integrative genomic and transcriptomic profiling of 230 patients with malignant solid tumors (the " primary cohort") and 18 patients with recurrent or otherwise difficult-to-treat nonmalignant conditions (the "secondary cohort"). The integrative workflow for the primary cohort enabled the identification of clinically significant single nucleotide variants, small insertions/deletions, and fusion genes, which were found in 55% and 28% of patients, respectively. For 38% of patients, molecularly informed treatment recommendations were made. In the secondary cohort, known or potentially driving alteration was detected in 89% of cases, including a suspected novel causal gene for patients with inclusion body infantile digital fibromatosis. Furthermore, 47% of findings also brought therapeutic implications for subsequent management. Across both cohorts, changes or refinements to the original histopathological diagnoses were achieved in 4% of cases. Our study demonstrates the efficacy of integrating advanced genomic and transcriptomic analyses to identify therapeutic targets, refine diagnoses, and optimize treatment strategies for challenging pediatric and young adult malignancies and underscores the need for broad implementation of precision oncology in clinical settings.
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