COST AND COMPARATIVE EFFECTIVENESS OF A GENOMIC CLASSIFIER FOR PROSTATE CANCER TREATMENT DECISIONS
Wednesday, October 22, 2014
Jennifer E. Mason, PhD1, Adam Dicker, MD, PhD
2, Christine Buerki, PhD
3, Elai Davicioni, PhD
3, Robert Den, MD
2 and Timothy Showalter, MD
1, (1)University of Virginia, Charlottesville, VA, (2)Thomas Jefferson University, Philadelphia, PA, (3)GenomeDx Biosciences Inc., Vancouver, BC, Canada
Purpose:
To evaluate the cost
effectiveness of genomic classifier (GC) risk-based treatment decisions for
prostate cancer patients post radical prostatectomy (RP).
Methods:
We present an
individualized decision analysis model to quantify the change in clinical
outcomes and costs of post RP treatment uptake based on three scenarios: usual
care based on percentages of adjuvant and salvage therapy reported in the
literature, 100% adjuvant therapy utilization, and GC risk-based decisions. We
first developed a Markov model for prostate cancer progression after RP based
upon average, population-level probabilities. We then evaluated outcomes in
this model when individual GC risk probabilities (5 year probabilities of distant
metastasis) were used for each individual within a simulated cohort. We used a
cohort simulation approach with a cohort of 139 patients with GC risk
probabilities from Thomas Jefferson University. For each comparison, we used
the bootstrap method of sampling with replacement to choose each patient to
pass through the Markov model. GC risk-based treatment decisions were based on
a study assessing urologist treatment recommendations following RP in the
adjuvant and salvage settings. Transition probabilities, costs, and utilities
were taken from secondary sources.
Results:
Usual care resulted
in 63.1% PSA recurrence-free at 5 years and an average over the 10 year post-RP
horizon of 9.07 life years (LYs), 7.69 quality-adjusted life years (QALYs), and
$21,980 in treatment costs. GC risk-based treatment resulted in 73.3%
recurrence-free at 5 years, 9.11 LYs, 7.61 QALYs, and $27,611 in treatment
costs without the cost of the GC test. Under 100% adjuvant therapy, 82.3% of
patients were recurrence-free at 5 years, and patients had an average of 9.13
LYs, 6.85 QALYs, and $36,549 in treatment costs. As seen in the figure below,
the GC risk-based treatment remains pareto-optimal when the GC test is
≤$8,938. Compared to 100% adjuvant therapy, GC risk-based treatment increases
QALYs by 0.76 QALYs and is cost saving for a GC test ≤$8,938.
Conclusions:
GC risk-based
treatment provides a balance of improvement in clinical outcomes and LYs over
usual care, and increased QALYs and reduced costs compared to providing
adjuvant therapy to 100% of patients. Our model's individualized decision
analysis framework can be extended to include other patient-specific factors
including treatment preferences and response to therapy.