Cost-effectiveness of screening guidelines to prevent heart failure in childhood cancer survivors: A report from the Childhood Cancer Survivor Study (CCSS).

Authors

null

Matthew J. Ehrhardt

St. Jude Children's Research Hospital, Memphis, TN

Matthew J. Ehrhardt , Zachary J. Ward , Qi Liu , Aeysha Chaudhry , Anju Nohria , William L. Border , Leslie L. Robison , Gregory T. Armstrong , Yutaka Yasui , Melissa M. Hudson , Lisa Diller , Saro Armenian , Jennifer Yeh

Organizations

St. Jude Children's Research Hospital, Memphis, TN, Harvard T.H. Chan School of Public Health, Boston, MA, University of Alberta, Edmonton, AB, Canada, Boston Children's Hospital, Boston, MA, Brigham and Women's Hospital Heart and Vascular Center, Boston, MA, Emory University, Atlanta, GA, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, City of Hope Comprehensive Cancer Center, Duarte, CA, Boston Children's Hospital and Harvard Medical School, Boston, MA

Research Funding

U.S. National Institutes of Health
American Lebanese Syrian Associated Charities

Background: Childhood cancer survivors treated with anthracyclines or chest radiation therapy (RT) are at risk for left ventricular dysfunction (LVD) and subsequent heart failure (HF). The International Guideline Harmonization Group (IGHG) recommends risk-based screening echocardiograms for LVD, but evidence supporting its frequency and cost-effectiveness is limited. Methods: Using data from the CCSS, we developed a microsimulation model of the clinical course of LVD and HF to estimate long-term health and economic outcomes associated with screening for IGHG-defined risk groups (low [anthracycline 1-99 mg/m2 and/or RT < 15 Gy], moderate [100 to < 250 mg/m2 or 15 to < 35 Gy], high [≥ 250 mg/m2 or ≥ 35 Gy or (≥ 100 mg/m2 and ≥ 15 Gy)]). We compared 1, 2, and 5-year interval-based screening to no screening. Screening performance and pharmacological treatment effectiveness were based on published studies. Costs and quality of life weights were based on US averages and published studies. Outcomes included lifetime HF risk, quality-adjusted life years (QALYs), lifetime costs, and incremental cost-effectiveness ratios (ICERs). Strategies with ICERs < $100,000/QALY gained were considered cost-effective. Results: Among the IGHG risk groups, the lifetime HF risk in the absence of screening was 37% (high), 25% (moderate) and 17% (low). Screening every 2 or 5 years was cost-effective for the high-risk group, and every 5 years for the moderate-risk group. In contrast, routine screening may not be cost-effective for the low risk group, representing ~40% of those for whom screening is currently recommended. Conclusions: Our findings can inform screening guidelines and suggest that LVD/HF surveillance for low-risk survivors warrants careful consideration.

Risk groupScreening interval, yearsAbsolute lifetime HF risk reduction, %aLifetime costs, $bICER, $/QALY
HighNo screening2,130
52.14,52026,780
23.17,23055,840
13.711,220138,040
ModerateNo screening1,020
51.43,45055,450
22.26,340124,770
12.610,680309,510
LowNo screening570
51.02,990101,330
21.55,940234,190
11.810,390570,310

a Relative to none; b Discounted at 3% annually

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Pediatric Oncology

Track

Pediatric Oncology

Sub Track

Survivorship

Citation

J Clin Oncol 37, 2019 (suppl; abstr 10052)

DOI

10.1200/JCO.2019.37.15_suppl.10052

Abstract #

10052

Poster Bd #

434

Abstract Disclosures