Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital

Next-generation sequencing (NGS) can be used to detect tumor-specific genomic alterations. This retrospective single-center study aims to assess the application of an extensive NGS panel to identify actionable alterations and initiate matched targeted treatment for patients with advanced cancer. We...

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Main Authors: Laure-Anne Teuwen, Evelyne Roets, Pieter D’Hoore, Patrick Pauwels, Hans Prenen
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/13/9/1619
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author Laure-Anne Teuwen
Evelyne Roets
Pieter D’Hoore
Patrick Pauwels
Hans Prenen
author_facet Laure-Anne Teuwen
Evelyne Roets
Pieter D’Hoore
Patrick Pauwels
Hans Prenen
author_sort Laure-Anne Teuwen
collection DOAJ
description Next-generation sequencing (NGS) can be used to detect tumor-specific genomic alterations. This retrospective single-center study aims to assess the application of an extensive NGS panel to identify actionable alterations and initiate matched targeted treatment for patients with advanced cancer. We analyzed genomic alterations in solid tumor biopsies from 464 patients with advanced cancer with the Foundation Medicine assay (FoundationOne<sup>®</sup>CDx). Therapeutic implications were determined using the Memorial Sloan Kettering Precision Oncology Knowledge Base (OncoKB) classification. The FoundationOne<sup>®</sup>CDx was successfully applied in 464/521 patients (89%). The most common altered genes were TP53 (61%), KRAS (20%), CDKN2A (20%), TERT (16%), and APC (16%). Among the 419 patients with successfully analyzed tumor mutational burden (TMB), 43 patients presented with a high TMB (≥10 mutations/megabase). Out of the 126 patients with an actionable target, 40 patients received matched treatment (32%) of which 17 were within a clinical trial. This study shows that the application of NGS is feasible in an academic center and increases the detection of actionable alterations and identification of patients eligible for targeted treatment or immunotherapy regardless of tumor histology. Strategies such as early referral for NGS, inclusion in clinical (basket) trials, and the development of new targeted drugs are necessary to improve the matched treatment rate.
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spelling doaj.art-3ba29aae21a2449b854e10def7befe6e2023-11-17T22:46:09ZengMDPI AGDiagnostics2075-44182023-05-01139161910.3390/diagnostics13091619Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic HospitalLaure-Anne Teuwen0Evelyne Roets1Pieter D’Hoore2Patrick Pauwels3Hans Prenen4Department of Oncology, Antwerp University Hospital, Drie Eikenstraat 655, 2650 Edegem, BelgiumDepartment of Oncology, Antwerp University Hospital, Drie Eikenstraat 655, 2650 Edegem, BelgiumDepartment of Oncology, Antwerp University Hospital, Drie Eikenstraat 655, 2650 Edegem, BelgiumDepartment of Pathology, Antwerp University Hospital, Drie Eikenstraat 655, 2650 Edegem, BelgiumDepartment of Oncology, Antwerp University Hospital, Drie Eikenstraat 655, 2650 Edegem, BelgiumNext-generation sequencing (NGS) can be used to detect tumor-specific genomic alterations. This retrospective single-center study aims to assess the application of an extensive NGS panel to identify actionable alterations and initiate matched targeted treatment for patients with advanced cancer. We analyzed genomic alterations in solid tumor biopsies from 464 patients with advanced cancer with the Foundation Medicine assay (FoundationOne<sup>®</sup>CDx). Therapeutic implications were determined using the Memorial Sloan Kettering Precision Oncology Knowledge Base (OncoKB) classification. The FoundationOne<sup>®</sup>CDx was successfully applied in 464/521 patients (89%). The most common altered genes were TP53 (61%), KRAS (20%), CDKN2A (20%), TERT (16%), and APC (16%). Among the 419 patients with successfully analyzed tumor mutational burden (TMB), 43 patients presented with a high TMB (≥10 mutations/megabase). Out of the 126 patients with an actionable target, 40 patients received matched treatment (32%) of which 17 were within a clinical trial. This study shows that the application of NGS is feasible in an academic center and increases the detection of actionable alterations and identification of patients eligible for targeted treatment or immunotherapy regardless of tumor histology. Strategies such as early referral for NGS, inclusion in clinical (basket) trials, and the development of new targeted drugs are necessary to improve the matched treatment rate.https://www.mdpi.com/2075-4418/13/9/1619advanced cancergenomic profilingnext-generation sequencingOncoKB classificationtargeted therapy
spellingShingle Laure-Anne Teuwen
Evelyne Roets
Pieter D’Hoore
Patrick Pauwels
Hans Prenen
Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital
Diagnostics
advanced cancer
genomic profiling
next-generation sequencing
OncoKB classification
targeted therapy
title Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital
title_full Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital
title_fullStr Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital
title_full_unstemmed Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital
title_short Comprehensive Genomic Profiling and Therapeutic Implications for Patients with Advanced Cancers: The Experience of an Academic Hospital
title_sort comprehensive genomic profiling and therapeutic implications for patients with advanced cancers the experience of an academic hospital
topic advanced cancer
genomic profiling
next-generation sequencing
OncoKB classification
targeted therapy
url https://www.mdpi.com/2075-4418/13/9/1619
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