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Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan
BACKGROUND: Whole exome sequencing and RNA sequencing (WES/RNASeq) should now be implemented in the clinical practice in order to increase access to optimal care for cancer patients. Providing results to Tumour Boards in a relevant time frame—that is, compatible with the clinical pathway—is crucial....
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383956/ https://www.ncbi.nlm.nih.gov/pubmed/32713836 http://dx.doi.org/10.1136/esmoopen-2020-000744 |
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author | Auzanneau, Céline Bacq, Delphine Bellera, Carine Blons, Hélène Boland, Anne Boucheix, Marlène Bourdon, Aurélien Chollet, Emmanuelle Chomienne, Christine Deleuze, Jean-François Delmas, Christelle Dinart, Derek Espérou, Hélène Geillon, Flore Geneste, Damien Italiano, Antoine Jean, Delphine Khalifa, Emmanuel Laizet, Yec'han Laurent-Puig, Pierre Lethimonnier, Franck Lévy-Marchal, Claire Lucchesi, Carlo Malle, Carine Mancini, Pierre Mathoulin-Pélissier, Simone Meyer, Vincent Marie-Ange, Palomares Perkins, Géraldine Sellan-Albert, Sabrina Soubeyran, Isabelle Wallet, Cédric |
author_facet | Auzanneau, Céline Bacq, Delphine Bellera, Carine Blons, Hélène Boland, Anne Boucheix, Marlène Bourdon, Aurélien Chollet, Emmanuelle Chomienne, Christine Deleuze, Jean-François Delmas, Christelle Dinart, Derek Espérou, Hélène Geillon, Flore Geneste, Damien Italiano, Antoine Jean, Delphine Khalifa, Emmanuel Laizet, Yec'han Laurent-Puig, Pierre Lethimonnier, Franck Lévy-Marchal, Claire Lucchesi, Carlo Malle, Carine Mancini, Pierre Mathoulin-Pélissier, Simone Meyer, Vincent Marie-Ange, Palomares Perkins, Géraldine Sellan-Albert, Sabrina Soubeyran, Isabelle Wallet, Cédric |
author_sort | Auzanneau, Céline |
collection | PubMed |
description | BACKGROUND: Whole exome sequencing and RNA sequencing (WES/RNASeq) should now be implemented in the clinical practice in order to increase access to optimal care for cancer patients. Providing results to Tumour Boards in a relevant time frame—that is, compatible with the clinical pathway—is crucial. Assessing the feasibility of this implementation in the French care system is the primary objective of the Multipli study, as one of the four pilot projects of the national France Genomic Medicine 2025 (FGM 2025) plan. The Multipli study encompasses two innovative trials which will be driven in around 2400 patients suffering from a soft-tissue sarcoma (Multisarc) or a metastatic colorectal carcinoma (Acompli). METHODS: Prior to launching the FGM 2025 cancer pilot study itself, the performance of the Multipli genomic workflow has been evaluated through each step, from the samples collection to the Molecular Tumour Board (MTB) report. Two Multipli-assigned INCa-labelled molecular genetics centres, the CEA-CNRGH sequencing platform and the Institut Bergonié’s Bioinformatics Platform were involved in a multicentric study. The duration of each step of the genomic workflow was monitored and bottlenecks were identified. RESULTS: Thirty barriers which could affect the quality of the samples, sequencing results and the duration of each step of the genomic pathway were identified and mastered. The global turnaround time from the sample reception to the MTB report was of 44 calendar days. CONCLUSION: Our results demonstrate the feasibility of tumour genomic analysis by WES/RNASeq within a time frame compatible with the current cancer patient care. Lessons learnt from the Multipli WES/RNASeq Platforms Workflow Study will constitute guidelines for the forthcoming Multipli study and more broadly for the future clinical routine practice in the first two France Genomic Medicine 2025 platforms. |
format | Online Article Text |
id | pubmed-7383956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-73839562020-08-10 Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan Auzanneau, Céline Bacq, Delphine Bellera, Carine Blons, Hélène Boland, Anne Boucheix, Marlène Bourdon, Aurélien Chollet, Emmanuelle Chomienne, Christine Deleuze, Jean-François Delmas, Christelle Dinart, Derek Espérou, Hélène Geillon, Flore Geneste, Damien Italiano, Antoine Jean, Delphine Khalifa, Emmanuel Laizet, Yec'han Laurent-Puig, Pierre Lethimonnier, Franck Lévy-Marchal, Claire Lucchesi, Carlo Malle, Carine Mancini, Pierre Mathoulin-Pélissier, Simone Meyer, Vincent Marie-Ange, Palomares Perkins, Géraldine Sellan-Albert, Sabrina Soubeyran, Isabelle Wallet, Cédric ESMO Open Original Research BACKGROUND: Whole exome sequencing and RNA sequencing (WES/RNASeq) should now be implemented in the clinical practice in order to increase access to optimal care for cancer patients. Providing results to Tumour Boards in a relevant time frame—that is, compatible with the clinical pathway—is crucial. Assessing the feasibility of this implementation in the French care system is the primary objective of the Multipli study, as one of the four pilot projects of the national France Genomic Medicine 2025 (FGM 2025) plan. The Multipli study encompasses two innovative trials which will be driven in around 2400 patients suffering from a soft-tissue sarcoma (Multisarc) or a metastatic colorectal carcinoma (Acompli). METHODS: Prior to launching the FGM 2025 cancer pilot study itself, the performance of the Multipli genomic workflow has been evaluated through each step, from the samples collection to the Molecular Tumour Board (MTB) report. Two Multipli-assigned INCa-labelled molecular genetics centres, the CEA-CNRGH sequencing platform and the Institut Bergonié’s Bioinformatics Platform were involved in a multicentric study. The duration of each step of the genomic workflow was monitored and bottlenecks were identified. RESULTS: Thirty barriers which could affect the quality of the samples, sequencing results and the duration of each step of the genomic pathway were identified and mastered. The global turnaround time from the sample reception to the MTB report was of 44 calendar days. CONCLUSION: Our results demonstrate the feasibility of tumour genomic analysis by WES/RNASeq within a time frame compatible with the current cancer patient care. Lessons learnt from the Multipli WES/RNASeq Platforms Workflow Study will constitute guidelines for the forthcoming Multipli study and more broadly for the future clinical routine practice in the first two France Genomic Medicine 2025 platforms. BMJ Publishing Group 2020-07-26 /pmc/articles/PMC7383956/ /pubmed/32713836 http://dx.doi.org/10.1136/esmoopen-2020-000744 Text en © Author (s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ on behalf of the European Society for Medical Oncology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and any changes made are indicated. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Research Auzanneau, Céline Bacq, Delphine Bellera, Carine Blons, Hélène Boland, Anne Boucheix, Marlène Bourdon, Aurélien Chollet, Emmanuelle Chomienne, Christine Deleuze, Jean-François Delmas, Christelle Dinart, Derek Espérou, Hélène Geillon, Flore Geneste, Damien Italiano, Antoine Jean, Delphine Khalifa, Emmanuel Laizet, Yec'han Laurent-Puig, Pierre Lethimonnier, Franck Lévy-Marchal, Claire Lucchesi, Carlo Malle, Carine Mancini, Pierre Mathoulin-Pélissier, Simone Meyer, Vincent Marie-Ange, Palomares Perkins, Géraldine Sellan-Albert, Sabrina Soubeyran, Isabelle Wallet, Cédric Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan |
title | Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan |
title_full | Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan |
title_fullStr | Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan |
title_full_unstemmed | Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan |
title_short | Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan |
title_sort | feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the france genomic medicine 2025 plan |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383956/ https://www.ncbi.nlm.nih.gov/pubmed/32713836 http://dx.doi.org/10.1136/esmoopen-2020-000744 |
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