Cost-effectiveness analysis of selective first-line use of biologics for unresectable RAS wild-type left-sided metastatic colorectal cancer

Curr Oncol. 2019 Oct;26(5):e597-e609. doi: 10.3747/co.26.4843. Epub 2019 Oct 1.

Abstract

Background: Evidence from a retrospective analysis of multiple large phase iii trials suggested that primary tumour location (ptl) in RAS wild-type metastatic colorectal cancer (wtRAS mcrc) might have predictive value with respect to response to drug therapies. Recent studies also show a potential preferential benefit for epidermal growth factor inhibitors (egfris) for left-sided tumours. In the present study, we aimed to determine the incremental cost-effectiveness ratio (icer) for the first-line use of an egfri for patients with left-sided wtRAS mcrc.

Methods: We developed a state-transition model to determine the cost effectiveness of alternative treatment strategies in patients with left-sided mcrc:■ Standard of care■ Use of an egfri in first-line therapyThe cohort for the study consisted of patients diagnosed with unresectable wtRAS mcrc with an indication for chemotherapy and previously documented ptl. Model parameters were obtained from the published literature and calibration. The perspective was that of a provincial ministry of health in Canada. We used a 5-year time horizon and an annual discount rate of 1.5%.

Results: Selecting patients for first-line egfri treatment based on left-sided location of their colorectal primary tumour was more effective than the standard of care, resulting in an increase in quality-adjusted life-years (qalys) of 0.226 (or 0.644 life-years gained). However, the strategy was also more expensive, costing an average of $60,639 more per patient treated. The resulting icer was $268,094 per qaly. A 35% price reduction in the cost of egfri would be needed to make this strategy cost-effective at a willingness-to-pay threshold (wtp) of $100,000 per qaly.

Conclusions: Selective use of an egfri based on ptl was more cost-effective than unselected use of those agents; however, based on traditional wtp thresholds, it was still not cost-effective. While awaiting the elucidation of more precise predictive biomarkers that might improve cost-effectiveness, the price of egfris could be reduced to meet the wtp threshold.

Keywords: Cost-effectiveness analyses; EGFR inhibitors; RAS wild-type; colorectal cancer; metastatic; primary tumour location.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / economics*
  • Antineoplastic Agents / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / economics
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bevacizumab / economics*
  • Bevacizumab / therapeutic use
  • Biological Products / economics*
  • Biological Products / therapeutic use
  • Camptothecin / analogs & derivatives
  • Camptothecin / economics
  • Camptothecin / therapeutic use
  • Cetuximab / economics
  • Cetuximab / therapeutic use
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / economics*
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / pathology
  • Cost-Benefit Analysis
  • ErbB Receptors / antagonists & inhibitors
  • Fluorouracil / economics
  • Fluorouracil / therapeutic use
  • Humans
  • Leucovorin / economics
  • Leucovorin / therapeutic use
  • Organoplatinum Compounds / economics
  • Organoplatinum Compounds / therapeutic use
  • Protein Kinase Inhibitors / economics*
  • Protein Kinase Inhibitors / therapeutic use
  • ras Proteins / genetics

Substances

  • Antineoplastic Agents
  • Biological Products
  • Organoplatinum Compounds
  • Protein Kinase Inhibitors
  • Bevacizumab
  • EGFR protein, human
  • ErbB Receptors
  • ras Proteins
  • Cetuximab
  • Leucovorin
  • Fluorouracil
  • Camptothecin

Supplementary concepts

  • Folfox protocol
  • IFL protocol

Grants and funding