Cost-Effectiveness Analysis of Chemoradiation Therapy Versus Transoral Robotic Surgery for Human Papillomavirus-Associated, Clinical N2 Oropharyngeal Cancer

被引:32
|
作者
Sher, David J. [1 ]
Fidler, Mary Jo [2 ]
Tishler, Roy B. [3 ,4 ]
Stenson, Kerstin [5 ]
al-Khudari, Samer [5 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, 5801 Lake Forest Rd, Dallas, TX 75390 USA
[2] Rush Univ, Med Ctr, Sect Med Oncol, Chicago, IL 60612 USA
[3] Brigham & Womens Hosp, Dept Radiat Oncol, 75 Francis St, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Rush Univ, Med Ctr, Dept Otolaryngol, Chicago, IL 60612 USA
关键词
SQUAMOUS-CELL CARCINOMA; RADIATION-THERAPY; IMPROVED SURVIVAL; POSITIVE HEAD; ONCOLOGY; RADIOTHERAPY; GASTROSTOMY; OUTCOMES; IMPACT; TRIAL;
D O I
10.1016/j.ijrobp.2015.11.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To perform a cost-effectiveness analysis of primary chemoradiation therapy (CRT) versus transoral robotic surgery (TORS) for clinical N2, human papillomavirus (HPV)-positive oropharyngeal carcinoma. Methods and Materials: We developed a Markov model to describe the health states after treatment with CRT or TORS, followed by adjuvant radiation therapy or CRT in the presence of high-risk pathology (positive margins or extracapsular extension). Outcomes, toxicities, and costs were extracted from the literature. One-way sensitivity analyses (SA) were performed over a wide range of parameters, as were 2-way SA between the key variables. Probabilistic SA and value of information studies were performed over key parameters. Results: The expected quality-adjusted life years (QALYs)/total costs for CRT and TORS were 7.31/$ 50,100 and 7.29/$62,200, respectively, so that CRT dominated TORS. In SA, primary CRT was almost always cost-effective up to a societal willingness-to-pay of $200,000/QALY, unless the locoregional recurrence risk after TORS was 30% to 50% lower, at which point it became cost effective at a willingness-to-pay of $ 50-100,000/QALY. Probabilistic SA confirmed the importance of locoregional recurrence risk, and the value of information in precisely knowing this parameter was more than $ 7M per year. If the long-term utility after TORS was 0.03 lower than CRT, CRT was cost-effective over nearly any assumption. Conclusions: Under nearly all assumptions, primary CRT was the cost-effective therapy for HPV-associated, clinical N2 OPC. However, in the hypothetical event of a large relative improvement in LRR with surgery and equivalent long-term utilities, primary TORS would become the higher-value treatment, arguing for prospective, comparative study of the 2 paradigms. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:512 / 522
页数:11
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