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A time-and-motion approach to micro-costing of high-throughput genomic assays.
Costa, S; Regier, D A; Meissner, B; Cromwell, I; Ben-Neriah, S; Chavez, E; Hung, S; Steidl, C; Scott, D W; Marra, M A; Peacock, S J; Connors, J M.
Afiliação
  • Costa S; Canadian Centre for Applied Research in Cancer Control, Vancouver, BC; Department of Cancer Control Research, BC Cancer Agency, Vancouver, BC.
  • Regier DA; Canadian Centre for Applied Research in Cancer Control, Vancouver, BC; Department of Cancer Control Research, BC Cancer Agency, Vancouver, BC; School of Population and Public Health, University of British Columbia, Vancouver, BC.
  • Meissner B; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC.
  • Cromwell I; Canadian Centre for Applied Research in Cancer Control, Vancouver, BC; Department of Cancer Control Research, BC Cancer Agency, Vancouver, BC.
  • Ben-Neriah S; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC.
  • Chavez E; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC.
  • Hung S; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC.
  • Steidl C; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC.
  • Scott DW; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC; Department of Medicine, University of British Columbia, Vancouver, BC.
  • Marra MA; Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, University of British Columbia, Vancouver, BC; Department of Medical Genetics, University of British Columbia, Vancouver, BC.
  • Peacock SJ; Canadian Centre for Applied Research in Cancer Control, Vancouver, BC; Department of Cancer Control Research, BC Cancer Agency, Vancouver, BC; Faculty of Health Sciences, Simon Fraser University, Burnaby, BC.
  • Connors JM; Centre for Lymphoid Cancer, BC Cancer Agency, University of British Columbia, Vancouver, BC; Department of Medicine, University of British Columbia, Vancouver, BC.
Curr Oncol ; 23(5): 304-313, 2016 Oct.
Article em En | MEDLINE | ID: mdl-27803594
ABSTRACT

BACKGROUND:

Genomic technologies are increasingly used to guide clinical decision-making in cancer control. Economic evidence about the cost-effectiveness of genomic technologies is limited, in part because of a lack of published comprehensive cost estimates. In the present micro-costing study, we used a time-and-motion approach to derive cost estimates for 3 genomic assays and processes-digital gene expression profiling (gep), fluorescence in situ hybridization (fish), and targeted capture sequencing, including bioinformatics analysis-in the context of lymphoma patient management.

METHODS:

The setting for the study was the Department of Lymphoid Cancer Research laboratory at the BC Cancer Agency in Vancouver, British Columbia. Mean per-case hands-on time and resource measurements were determined from a series of direct observations of each assay. Per-case cost estimates were calculated using a bottom-up costing approach, with labour, capital and equipment, supplies and reagents, and overhead costs included.

RESULTS:

The most labour-intensive assay was found to be fish at 258.2 minutes per case, followed by targeted capture sequencing (124.1 minutes per case) and digital gep (14.9 minutes per case). Based on a historical case throughput of 180 cases annually, the mean per-case cost (2014 Canadian dollars) was estimated to be $1,029.16 for targeted capture sequencing and bioinformatics analysis, $596.60 for fish, and $898.35 for digital gep with an 807-gene code set.

CONCLUSIONS:

With the growing emphasis on personalized approaches to cancer management, the need for economic evaluations of high-throughput genomic assays is increasing. Through economic modelling and budget-impact analyses, the cost estimates presented here can be used to inform priority-setting decisions about the implementation of such assays in clinical practice.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Tipo de estudo: Health_economic_evaluation / Prognostic_studies Idioma: En Revista: Curr Oncol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Tipo de estudo: Health_economic_evaluation / Prognostic_studies Idioma: En Revista: Curr Oncol Ano de publicação: 2016 Tipo de documento: Article