Real-World Cost-Effectiveness of Bevacizumab With First-Line Combination Chemotherapy in Patients With Metastatic Colorectal Cancer: Population-Based Retrospective Cohort Studies in Three Canadian Provinces

Author:

Pataky Reka E.12ORCID,Beca Jaclyn23ORCID,Tran David4,Dai Wei Fang23,Dvorani Erind5,Isaranuwatchai Wanrudee26,Peacock Stuart127,Alvi Riaz4,Cheung Winson Y.8,Earle Craig C.5910,Gavura Scott3,Chan Kelvin K. W.2310ORCID

Affiliation:

1. BC Cancer, Vancouver, British Columbia, Canada

2. Canadian Centre for Applied Research in Cancer Control, Vancouver, British Columbia and Toronto, Ontario, Canada

3. Cancer Care Ontario, Toronto, Ontario, Canada

4. Saskatchewan Cancer Agency, Saskatoon, Saskatchewan, Canada

5. ICES, Toronto, Ontario, Canada

6. St. Michael’s Hospital, Toronto, Ontario, Canada

7. Faculty of Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada

8. Cancer Care Alberta, Calgary, Alberta, Canada

9. Canadian Partnership Against Cancer, Toronto, Ontario, Canada

10. Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada

Abstract

Background. Real-world evidence can be a valuable tool when clinical trial data are incomplete or uncertain. Bevacizumab was adopted as first-line therapy for metastatic colorectal cancer (mCRC) based on significant survival improvements in initial clinical trials; however, survival benefit diminished in subsequent analyses. Consequently, there is uncertainty surrounding the cost-effectiveness of bevacizumab therapy achieved in practice. Objective. To assess real-world cost-effectiveness of first-line bevacizumab with irinotecan-based chemotherapy versus irinotecan-based chemotherapy alone for mCRC in British Columbia (BC), Saskatchewan, and Ontario, Canada. Methods. Using provincial cancer registries and linked administrative databases, we identified mCRC patients who initiated publicly funded irinotecan-based chemotherapy, with or without bevacizumab, in 2000 to 2015. We compared bevacizumab-treated patients to historical controls (treated before bevacizumab funding) and contemporaneous controls (receiving chemotherapy without bevacizumab), using inverse-probability-of-treatment weighting with propensity scores to balance baseline covariates. We calculated incremental cost-effectiveness ratios (ICER) using 5-year cost and survival adjusted for censoring, with bootstrapping to characterize uncertainty. We also conducted one-way sensitivity analysis for key drivers of cost-effectiveness. Results. The cohorts included 12,112 (Ontario), 1,161 (Saskatchewan), and 2,977 (BC) patients. Bevacizumab significantly increased treatment costs, with mean ICERs between $78,000 and $84,000/LYG (life-year gained) in the contemporaneous comparisons and $75,000 and $101,000/LYG in the historical comparisons. Reducing the cost of bevacizumab by 50% brought ICERs in all comparisons below $61,000/LYG. Limitations. Residual confounding in observational data may bias results, while the use of original list prices overestimates current bevacizumab cost. Conclusion. The addition of bevacizumab to irinotecan-based chemotherapy extended survival for mCRC patients but at significant cost. At original list prices bevacizumab can only be considered cost-effective with certainty at a willingness-to-pay threshold over $100,000/LYG, but price reductions or discounts have a significant impact on cost-effectiveness.

Publisher

SAGE Publications

Subject

Public Health, Environmental and Occupational Health,Health Policy

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