医学
成本-效用分析
化疗
阶段(地层学)
外科
肿瘤科
生殖细胞
成本分析
质量调整寿命年
内科学
精原细胞瘤
梅德林
重症监护医学
生殖细胞肿瘤
妇科
作者
Vidit Sharma,Stephen Anthony Boorjian,Kevin M. Wymer,Grace Ratcliff,John A. Graves,David F. Penson,Bradley C. Leibovich,Brian Addis Costello,Lance C. Pagliaro,Daniel Ari Barocas,Daniel D. Joyce
出处
期刊:The Journal of Urology
[Lippincott Williams & Wilkins]
日期:2026-09-18
卷期号:: 101097JU0000000000005317-101097JU0000000000005317
标识
DOI:10.1097/ju.0000000000005317
摘要
PURPOSE: Patients with marker negative stage IIA nonseminomatous germ cell tumor (NSGCT) may be treated with chemotherapy or retroperitoneal lymph node dissection (RPLND). Although both strategies have high cure rates, chemotherapy has higher long-term toxicities. In the absence of randomized trials, we conducted a cost-effectiveness analysis of chemotherapy vs RPLND for stage IIA NSGCT using a microsimulation approach. METHODS: A health transition state model compared open, nerve-sparing RPLND to 3 cycles of bleomycin, etoposide, and cisplatin chemotherapy for marker negative stage IIA NSGCT. Transition probabilities, utility values, and private payer costs for each health state were estimated from the literature. Primary outcomes were costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratio over a lifetime horizon. Sensitivity analyses identified clinically relevant parameters altering model conclusions. RESULTS: Using a simulated cohort of 300,000 patients with stage IIA NSGCT, total lifetime treatment costs were $50,735 for RPLND and $91,830 for chemotherapy. RPLND had 1.57 additional QALYs compared with chemotherapy. Thus, RPLND was the dominant strategy (lower cost and higher effectiveness), and chemotherapy was not cost-effective. On sensitivity analysis, chemotherapy only became cost-effective at edge cases when: the 3-year risk of progression after RPLND exceeded 27.8% (base case: 10%) or when chemotherapy toxicities were eliminated. CONCLUSIONS: RPLND results in improved QALYs at lower costs for patients with stage IIA NSGCT because of significant chronic toxicities from chemotherapy. As such, RPLND should be preferred for most patients with stage IIA NSGCT, although chemotherapy should be preferred for patients with a particularly higher risk of progression after RPLND.
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