Feasibility of whole-genome sequencing-based tumor diagnostics in routine pathology practice.

DNA sequencing cancer diagnostics precision oncology whole genome sequencing Biomarker

Journal

The Journal of pathology
ISSN: 1096-9896
Titre abrégé: J Pathol
Pays: England
ID NLM: 0204634

Informations de publication

Date de publication:
10 2022
Historique:
revised: 19 05 2022
received: 21 02 2022
accepted: 04 07 2022
pubmed: 7 7 2022
medline: 9 9 2022
entrez: 6 7 2022
Statut: ppublish

Résumé

The current increase in number and diversity of targeted anticancer agents poses challenges to the logistics and timeliness of molecular diagnostics (MolDx), resulting in underdiagnosis and treatment. Whole-genome sequencing (WGS) may provide a sustainable solution for addressing current as well as future diagnostic challenges. The present study therefore aimed to prospectively assess feasibility, validity, and value of WGS in routine clinical practice. WGS was conducted independently of, and in parallel with, standard of care (SOC) diagnostics on routinely obtained tumor samples from 1,200 consecutive patients with metastatic cancer. Results from both tests were compared and discussed in a dedicated tumor board. From 1,200 patients, 1,302 samples were obtained, of which 1,216 contained tumor cells. WGS was successful in 70% (854/1,216) of samples with a median turnaround time of 11 days. Low tumor purity (<20%) was the main reason for not completing WGS. WGS identified 99.2% and SOC MolDx 99.7% of the total of 896 biomarkers found in genomic regions covered by both tests. Actionable biomarkers were found in 603/848 patients (71%). Of the 936 associated therapy options identified by WGS, 343 were identified with SOC MolDx (36.6%). Biomarker-based therapy was started in 147 patients. WGS revealed 49 not previously identified pathogenic germline variants. Fresh-frozen, instead of formalin-fixed and paraffin-embedded, sample logistics were easily adopted as experienced by the professionals involved. WGS for patients with metastatic cancer is well feasible in routine clinical practice, successfully yielding comprehensive genomic profiling for the vast majority of patients. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Identifiants

pubmed: 35792649
doi: 10.1002/path.5988
pmc: PMC9546477
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

179-188

Informations de copyright

© 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

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Auteurs

Kris G Samsom (KG)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Luuk J Schipper (LJ)

Department of Molecular Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Oncode Institute, Office Jaarbeurs Innovation Mile (JIM), Utrecht, The Netherlands.

Paul Roepman (P)

Hartwig Medical Foundation, Amsterdam, The Netherlands.

Linda Jw Bosch (LJ)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Ferry Lalezari (F)

Department of Radiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Elisabeth G Klompenhouwer (EG)

Department of Radiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Adrianus J de Langen (AJ)

Department of Thoracic Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Tineke E Buffart (TE)

Department of Gastrointestinal Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Immy Riethorst (I)

Hartwig Medical Foundation, Amsterdam, The Netherlands.

Lieke Schoenmaker (L)

Hartwig Medical Foundation, Amsterdam, The Netherlands.

Daoin Schout (D)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Vincent van der Noort (V)

Department of Biometrics, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Jose G van den Berg (JG)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Ewart de Bruijn (E)

Hartwig Medical Foundation, Amsterdam, The Netherlands.

Jacobus Jm van der Hoeven (JJ)

Hartwig Medical Foundation, Amsterdam, The Netherlands.

Hans van Snellenberg (H)

Hartwig Medical Foundation, Amsterdam, The Netherlands.

Lizet E van der Kolk (LE)

Family Cancer Clinic, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Edwin Cuppen (E)

Oncode Institute, Office Jaarbeurs Innovation Mile (JIM), Utrecht, The Netherlands.
Hartwig Medical Foundation, Amsterdam, The Netherlands.
Center for Molecular Medicine, University Medical Centre Utrecht, Utrecht, The Netherlands.

Emile E Voest (EE)

Department of Molecular Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Oncode Institute, Office Jaarbeurs Innovation Mile (JIM), Utrecht, The Netherlands.
Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Gerrit A Meijer (GA)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Kim Monkhorst (K)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

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