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. 2022 Sep;21(3):e189-e195.
doi: 10.1016/j.clcc.2022.05.001. Epub 2022 May 11.

Cost-effectiveness of DPYD Genotyping Prior to Fluoropyrimidine-based Adjuvant Chemotherapy for Colon Cancer

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Cost-effectiveness of DPYD Genotyping Prior to Fluoropyrimidine-based Adjuvant Chemotherapy for Colon Cancer

Gabriel A Brooks et al. Clin Colorectal Cancer. 2022 Sep.

Abstract

Background: Adjuvant fluoropyrimidine-based chemotherapy substantially reduces recurrence and mortality after resection of stage 3 colon cancer. While standard doses of 5-fluorouracil and capecitabine are safe for most patients, the risk of severe toxicity is increased for the approximately 6% of patients with dihydropyimidine dehydrogenase (DPD) deficiency caused by pathogenic DPYD gene variants. Pre-treatment screening for pathogenic DPYD gene variants reduces severe toxicity but has not been widely adopted in the United States.

Methods: We conducted a cost-effectiveness analysis of DPYD genotyping prior to fluoropyrimidine-based adjuvant chemotherapy for stage 3 colon cancer, covering the c.1129-5923C>G (HapB3), c.1679T>G (*13), c.1905+1G>A (*2A), and c.2846A>T gene variants. We used a Markov model with a 5-year horizon, taking a United States healthcare perspective. Simulated patients with pathogenic DPYD gene variants received reduced-dose fluoropyrimidine chemotherapy. The primary outcome was the incremental cost-effectiveness ratio (ICER) for DPYD genotyping.

Results: Compared with no screening for DPD deficiency, DPYD genotyping increased per-patient costs by $78 and improved survival by 0.0038 quality-adjusted life years (QALYs), leading to an ICER of $20,506/QALY. In 1-way sensitivity analyses, The ICER exceeded $50,000 per QALY when the cost of the DPYD genotyping assay was greater than $286. In probabilistic sensitivity analysis using a willingness-to-pay threshold of $50,000/QALY DPYD genotyping was preferred to no screening in 96.2% of iterations.

Conclusion: Among patients receiving adjuvant chemotherapy for stage 3 colon cancer, screening for DPD deficiency with DPYD genotyping is a cost-effective strategy for preventing infrequent but severe and sometimes fatal toxicities of fluoropyrimidine chemotherapy.

Keywords: 5-fluorouracil; Capecitabine; DPD deficiency; Pharmacogenetics.

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Conflict of interest statement

Conflict of interest statement The authors attest that they have no financial conflicts of interest related to the topic of this research manuscript. Dr. Brooks reports consulting payments (unrelated to the topic of this manuscript) from CareCentrix, UnitedHealthcare, and Ipsen.

Figures

Figure 1.
Figure 1.
Structure of Markov model simulating adjuvant chemotherapy for stage 3 colon cancer aA subset of patients with grade 3–4 toxicity experience toxicity-related hospitalizations.
Figure 2.
Figure 2.
Monte Carlo plot of 100,000 model iterations from probabilistic sensitivity analysis Each plotted point represents an iteration of the probabilistic sensitivity analysis. The diagonal line indicates a willingness-to-pay (WTP) threshold of $50,000 and the ellipse represents the 95% confidence interval. DPYD genotyping is preferred to the no screening strategy for green points below the WTP threshold.

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