TY - JOUR
T1 - Cost of high-throughput sequencing (NGS) technologies
T2 - Literature review and insights
AU - Bayle, Arnaud
AU - Marino, Patricia
AU - Baffert, Sandrine
AU - Margier, Jennifer
AU - Bonastre, Julia
N1 - Publisher Copyright:
© 2023 Société Française du Cancer
PY - 2024/2/1
Y1 - 2024/2/1
N2 - Although high-throughput sequencing technologies (Next-Generation Sequencing [NGS]) are revolutionizing medicine, the estimation of their production cost for pricing/tariffication by health systems raises methodological questions. The objective of this review of cost studies of high-throughput sequencing techniques is to draw lessons for producing robust cost estimates of these techniques. We analyzed, using an eleven item analysis framework, micro-costing studies of high-throughput sequencing technologies (n = 17), including two studies conducted in the French context. The factors of variability between the studies that we identified were temporality (early evaluation of the innovation vs. evaluation of a mature technology), the choice of cost evaluation method (scope, micro- vs. gross-costing technique), the choice of production steps observed and the transposability of these studies. The lessons we have learned are that it is necessary to have a comprehensive vision of the sequencing production process by integrating all the steps from the collection of the biological sample to the delivery of the result to the clinician. It is also important to distinguish between what refers to the local context and what refers to the general context, by favouring the use of mixed methods to calculate costs. Finally, sensitivity analyses and periodic re-estimation of the costs of the techniques must be carried out in order to be able to revise the tariffs according to changes linked to the diffusion of the technology and to competition between reagent suppliers.
AB - Although high-throughput sequencing technologies (Next-Generation Sequencing [NGS]) are revolutionizing medicine, the estimation of their production cost for pricing/tariffication by health systems raises methodological questions. The objective of this review of cost studies of high-throughput sequencing techniques is to draw lessons for producing robust cost estimates of these techniques. We analyzed, using an eleven item analysis framework, micro-costing studies of high-throughput sequencing technologies (n = 17), including two studies conducted in the French context. The factors of variability between the studies that we identified were temporality (early evaluation of the innovation vs. evaluation of a mature technology), the choice of cost evaluation method (scope, micro- vs. gross-costing technique), the choice of production steps observed and the transposability of these studies. The lessons we have learned are that it is necessary to have a comprehensive vision of the sequencing production process by integrating all the steps from the collection of the biological sample to the delivery of the result to the clinician. It is also important to distinguish between what refers to the local context and what refers to the general context, by favouring the use of mixed methods to calculate costs. Finally, sensitivity analyses and periodic re-estimation of the costs of the techniques must be carried out in order to be able to revise the tariffs according to changes linked to the diffusion of the technology and to competition between reagent suppliers.
KW - Cancer
KW - Genetic sequencing
KW - Micro-costing studies
KW - NGS
UR - http://www.scopus.com/inward/record.url?scp=85174323720&partnerID=8YFLogxK
U2 - 10.1016/j.bulcan.2023.08.013
DO - 10.1016/j.bulcan.2023.08.013
M3 - Review article
AN - SCOPUS:85174323720
SN - 0007-4551
VL - 111
SP - 190
EP - 198
JO - Bulletin du Cancer
JF - Bulletin du Cancer
IS - 2
ER -