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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.
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.
Afiliação
  • Auzanneau C; Unité de pathologie moléculaire, Institut Bergonié, Bordeaux, France.
  • Bacq D; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Bellera C; Centre national de recherche en génétique humaine, Institut de biologie François-Jacob, Commissariat à l'énergie atomique et aux énergies alternatives, Evry, France.
  • Blons H; Institut de santé publique, d'épidémiologie et de développement, Université de Bordeaux, Bordeaux, France.
  • Boland A; CIC-EC1401/EUCLID, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Boucheix M; Service de pharmacogénétique et d'oncologie moléculaire, Hopital Europeen Georges Pompidou, Paris, France.
  • Bourdon A; U1147, Centre universitaire des Saint-Pères, Institut national de la santé et de la recherche médicale, Paris, France.
  • Chollet E; Centre national de recherche en génétique humaine, Institut de biologie François-Jacob, Commissariat à l'énergie atomique et aux énergies alternatives, Evry, France.
  • Chomienne C; Unité de pathologie moléculaire, Institut Bergonié, Bordeaux, France.
  • Deleuze JF; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Delmas C; Unité de bioinformatique, Institut Bergonié, Bordeaux, France.
  • Dinart D; ITMO Cancer, Alliance nationale pour les sciences de la vie et de la santé, Paris, France.
  • Espérou H; ITMO Cancer, Alliance nationale pour les sciences de la vie et de la santé, Paris, France christine.chomienne@inserm.fr.
  • Geillon F; Institut National du Cancer, Boulogne-Billancourt, France.
  • Geneste D; Centre national de recherche en génétique humaine, Institut de biologie François-Jacob, Commissariat à l'énergie atomique et aux énergies alternatives, Evry, France.
  • Italiano A; Centre de référence, d'innovation et d'expertise, US39, Commissariat à l'énergie atomique et aux énergies alternatives, Evry, France.
  • Jean D; Institut de santé publique, Pôle recherche clinique, Institut national de la santé et de la recherche médicale, Paris, France.
  • Khalifa E; Institut de santé publique, d'épidémiologie et de développement, Université de Bordeaux, Bordeaux, France.
  • Laizet Y; CIC-EC1401/EUCLID, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Laurent-Puig P; Institut de santé publique, Pôle recherche clinique, Institut national de la santé et de la recherche médicale, Paris, France.
  • Lethimonnier F; Fédération francophone de cancérologie digestive, Dijon, France.
  • Lévy-Marchal C; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Lucchesi C; Unité de bioinformatique, Institut Bergonié, Bordeaux, France.
  • Malle C; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Mancini P; Unités Essais cliniques de phase précoce et Sarcomes, Institut Bergonié, Bordeaux, France.
  • Mathoulin-Pélissier S; CIC-EC1401/EUCLID, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Meyer V; Unité de pathologie moléculaire, Institut Bergonié, Bordeaux, France.
  • Marie-Ange P; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Perkins G; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Sellan-Albert S; Unité de bioinformatique, Institut Bergonié, Bordeaux, France.
  • Soubeyran I; U1147, Centre universitaire des Saint-Pères, Institut national de la santé et de la recherche médicale, Paris, France.
  • Wallet C; Service de génétique médicale et clinique, Hopital Europeen Georges Pompidou, Paris, France.
ESMO Open ; 5(4)2020 07.
Article em En | MEDLINE | ID: mdl-32713836
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Temas: Cuidados_paliativos / Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Neoplasias Tipo de estudo: Clinical_trials / Guideline Limite: Humans País/Região como assunto: Europa Idioma: En Revista: ESMO Open Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Temas: Cuidados_paliativos / Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Neoplasias Tipo de estudo: Clinical_trials / Guideline Limite: Humans País/Região como assunto: Europa Idioma: En Revista: ESMO Open Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França