Long-term cost–effectiveness of Oncotype DX® versus current clinical practice from a Dutch cost perspective

Author:

Kip Michelle12,Monteban Helma3,Steuten Lotte14

Affiliation:

1. Panaxea BV, Health Economics & Reimbursement, Enschede, The Netherlands

2. Department of Health Technology & Services Research, University of Twente, Enschede, The Netherlands

3. Monteban Value Services, Amerongen, The Netherlands

4. Hutchinson Institute for Cancer Outcomes Research (HICOR), Fred Hutchinson Cancer Research Center, Seattle, WA, USA

Abstract

Introduction: This study analyzes the incremental cost–effectiveness of Oncotype DX® testing to support adjuvant chemotherapy recommendations, versus current clinical practice, for patients with estrogen receptor-positive (ER+), node-negative or micrometastatic (pN1mic) early-stage breast cancer in The Netherlands. Methods: Markov model projecting distant recurrence, survival, quality-adjusted life years (QALYs) and healthcare costs over a 30-year time horizon. Results: Oncotype DX was projected to increase QALYs by 0.11 (0.07–0.58) and costs with €1236 (range: -€142–€1236) resulting in an incremental cost–effectiveness ratio of €11,236/QALY under the most conservative scenario. Conclusion: Reallocation of adjuvant chemotherapy based on Oncotype DX testing is most likely a cost-effective use of scarce resources, improving long-term survival and QALYs at marginal or lower costs.

Publisher

Future Medicine Ltd

Subject

Health Policy

Reference50 articles.

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2. Economic Implications of 21-Gene Breast Cancer Risk Assay from the Perspective of an Israeli-Managed Health-Care Organization

3. American Society of Clinical Oncology Clinical Practice Guideline: Update on Adjuvant Endocrine Therapy for Women With Hormone Receptor–Positive Breast Cancer

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5. Nabon: Landelijke richtlijn mammacarcinoom 2012. www.oncoline.nl/mammacarcinoom

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