Literature DB >> 33765190

Whole exome sequencing in molecular diagnostics of cancer decreases over time: evidence from a cost analysis in the French setting.

I Borget1,2,3, J Bonastre1,2, Arnaud Bayle4,5,6, N Droin1,7, B Besse1, Z Zou1,2, Y Boursin8, S Rissel1, E Solary1,3, L Lacroix1,7,3, E Rouleau1.   

Abstract

OBJECTIVES: Although high-throughput sequencing is revolutionising medicine, data on the actual cost of whole exome sequencing (WES) applications are needed. We aimed at assessing the cost of WES at a French cancer institute in 2015 and 2018.
METHODS: Actual costs of WES application in oncology research were determined using both micro-costing and gross-costing for the years 2015 and 2018, before and after the acquisition of a new sequencer. The entire workflow process of a WES test was tracked, and the number and unit price of each resource were identified at the most detailed level, from library preparation to bioinformatics analyses. In addition, we conducted an ad hoc analysis of the bioinformatics storage costs of data issued from WES analyses.
RESULTS: The cost of WES has decreased substantially, from €1921 per sample (i.e. cost of €3842 per patient) in 2015 to €804 per sample (i.e. cost of €1,608 per patient) in 2018, representing a decrease of 58%. In the meantime, the cost of bioinformatics storage has increased from €19,836 to €200,711.
CONCLUSION: This study suggests that WES cost has decreased significantly in recent years. WES has become affordable, even though clinical utility and efficiency still need to be confirmed.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Cost analysis; Genomics; Micro-costing; Oncology; Whole exome sequencing

Year:  2021        PMID: 33765190     DOI: 10.1007/s10198-021-01293-1

Source DB:  PubMed          Journal:  Eur J Health Econ        ISSN: 1618-7598


  30 in total

1.  A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases.

Authors:  Kornelia Neveling; Ilse Feenstra; Christian Gilissen; Lies H Hoefsloot; Erik-Jan Kamsteeg; Arjen R Mensenkamp; Richard J T Rodenburg; Helger G Yntema; Liesbeth Spruijt; Sascha Vermeer; Tuula Rinne; Koen L van Gassen; Danielle Bodmer; Dorien Lugtenberg; Rick de Reuver; Wendy Buijsman; Ronny C Derks; Nienke Wieskamp; Bert van den Heuvel; Marjolijn J L Ligtenberg; Hannie Kremer; David A Koolen; Bart P C van de Warrenburg; Frans P M Cremers; Carlo L M Marcelis; Jan A M Smeitink; Saskia B Wortmann; Wendy A G van Zelst-Stams; Joris A Veltman; Han G Brunner; Hans Scheffer; Marcel R Nelen
Journal:  Hum Mutat       Date:  2013-10-18       Impact factor: 4.878

2.  Molecular Screening for Cancer Treatment Optimization (MOSCATO-01) in Pediatric Patients: A Single-Institutional Prospective Molecular Stratification Trial.

Authors:  Anne C Harttrampf; Ludovic Lacroix; Marc Deloger; Frederic Deschamps; Stephanie Puget; Nathalie Auger; Philippe Vielh; Pascale Varlet; Zsofia Balogh; Samuel Abbou; Adrien Allorant; Dominique Valteau-Couanet; Sabine Sarnacki; Louise Gamiche-Rolland; Guillaume Meurice; Veronique Minard-Colin; Jacques Grill; Laurence Brugieres; Christelle Dufour; Nathalie Gaspar; Stefan Michiels; Gilles Vassal; Jean-Charles Soria; Birgit Geoerger
Journal:  Clin Cancer Res       Date:  2017-07-21       Impact factor: 12.531

3.  High-Throughput Genomics and Clinical Outcome in Hard-to-Treat Advanced Cancers: Results of the MOSCATO 01 Trial.

Authors:  Christophe Massard; Stefan Michiels; Charles Ferté; Marie-Cécile Le Deley; Ludovic Lacroix; Antoine Hollebecque; Loic Verlingue; Ecaterina Ileana; Silvia Rosellini; Samy Ammari; Maud Ngo-Camus; Rastislav Bahleda; Anas Gazzah; Andrea Varga; Sophie Postel-Vinay; Yohann Loriot; Caroline Even; Ingrid Breuskin; Nathalie Auger; Bastien Job; Thierry De Baere; Frederic Deschamps; Philippe Vielh; Jean-Yves Scoazec; Vladimir Lazar; Catherine Richon; Vincent Ribrag; Eric Deutsch; Eric Angevin; Gilles Vassal; Alexander Eggermont; Fabrice André; Jean-Charles Soria
Journal:  Cancer Discov       Date:  2017-04-01       Impact factor: 39.397

4.  A pilot precision medicine trial for children with diffuse intrinsic pontine glioma-PNOC003: A report from the Pacific Pediatric Neuro-Oncology Consortium.

Authors:  Sabine Mueller; Payal Jain; Winnie S Liang; Lindsay Kilburn; Cassie Kline; Nalin Gupta; Eshini Panditharatna; Suresh N Magge; Bo Zhang; Yuankun Zhu; John R Crawford; Anu Banerjee; Kellie Nazemi; Roger J Packer; Claudia K Petritsch; Nathalene Truffaux; Alison Roos; Sara Nasser; Joanna J Phillips; David Solomon; Annette Molinaro; Angela J Waanders; Sara A Byron; Michael E Berens; John Kuhn; Javad Nazarian; Michael Prados; Adam C Resnick
Journal:  Int J Cancer       Date:  2019-04-03       Impact factor: 7.396

5.  The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.

Authors:  Joseph D Buxbaum; Mark J Daly; Bernie Devlin; Thomas Lehner; Kathryn Roeder; Matthew W State
Journal:  Neuron       Date:  2012-12-20       Impact factor: 17.173

Review 6.  Trametinib in the treatment of multiple malignancies harboring MEK1 mutations.

Authors:  Tong Lian; Changying Li; Haitao Wang
Journal:  Cancer Treat Rev       Date:  2019-10-14       Impact factor: 12.111

7.  Cost analysis of whole genome sequencing in German clinical practice.

Authors:  Marika Plöthner; Martin Frank; J-Matthias Graf von der Schulenburg
Journal:  Eur J Health Econ       Date:  2016-07-05

8.  Genome sequencing: a systematic review of health economic evidence.

Authors:  Martin Frank; Anne Prenzler; Roland Eils; J-Matthias Graf von der Schulenburg
Journal:  Health Econ Rev       Date:  2013-12-12

9.  Systematic review of basket trials, umbrella trials, and platform trials: a landscape analysis of master protocols.

Authors:  Jay J H Park; Ellie Siden; Michael J Zoratti; Louis Dron; Ofir Harari; Joel Singer; Richard T Lester; Kristian Thorlund; Edward J Mills
Journal:  Trials       Date:  2019-09-18       Impact factor: 2.279

Review 10.  Molecular profiling for precision cancer therapies.

Authors:  Eoghan R Malone; Marc Oliva; Peter J B Sabatini; Tracy L Stockley; Lillian L Siu
Journal:  Genome Med       Date:  2020-01-14       Impact factor: 11.117

View more
  2 in total

1.  Accurate recombination estimation from pooled genotyping and sequencing: a case study on barley.

Authors:  Michael Schneider; Federico Casale; Benjamin Stich
Journal:  BMC Genomics       Date:  2022-06-25       Impact factor: 4.547

2.  Mutation burden-orthogonal tumor genomic subtypes delineate responses to immune checkpoint therapy.

Authors:  Shiro Takamatsu; Junzo Hamanishi; J B Brown; Ken Yamaguchi; Koji Yamanoi; Kosuke Murakami; Osamu Gotoh; Seiichi Mori; Masaki Mandai; Noriomi Matsumura
Journal:  J Immunother Cancer       Date:  2022-07       Impact factor: 12.469

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.