Dranitsaris George, Yu Bo, King Jennifer, Kaura Satyin, Zhang Adams
Augmentium Pharma Consulting Inc., Toronto, ON, Canada.
Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
Clinicoecon Outcomes Res. 2015 May 12;7:249-56. doi: 10.2147/CEOR.S82194. eCollection 2015.
Paclitaxel and docetaxel are commonly used for metastatic breast cancer in the People's Republic of China. To improve the safety and efficacy of paclitaxel, an albumin-bound formulation (nab) is now available in the People's Republic of China (Abraxane(®)). To provide health economic data for the key stakeholders, a cost-utility analysis comparing nab-paclitaxel to docetaxel, both as alternatives to paclitaxel, was conducted.
A meta-analysis of clinical outcomes Phase III trials comparing nab-paclitaxel (260 mg/m(2) every [q] 3 weeks) or branded docetaxel (100 mg/m(2) q 3 weeks), to solvent-based branded paclitaxel (175 mg/m(2) q 3 weeks) was undertaken to provide safety and clinical data. Resource use data for the delivery of anticancer therapy and for the treatment of grade 3/4 toxicity was collected from a time and motion study conducted in three Chinese cancer centers and from a survey of clinicians. Using the Time Trade-Off technique, health utility estimates were derived from interviewing 28 breast cancer patients from one cancer center in the People's Republic of China. All costs were reported in 2014 US dollars.
Nab-paclitaxel had the most favorable safety profile, characterized with the lowest incidence of grade 3/4 neutropenia, febrile neutropenia, anemia, and stomatitis. When the median number of cycles delivered from the clinical trials was applied, nab-paclitaxel had a cost per course of $19,752 compared with $8,940 and $13,741 for paclitaxel and docetaxel, respectively. As an alternative to paclitaxel, the cost per quality-adjusted life-year (QALY) gained with nab-paclitaxel suggested better value than with docetaxel ($57,900 vs $130,600).
Nab-paclitaxel appears to be a cost-effective option compared with docetaxel and paclitaxel, for metastatic breast cancer in the People's Republic of China.
在中国,紫杉醇和多西他赛常用于转移性乳腺癌的治疗。为提高紫杉醇的安全性和疗效,一种白蛋白结合型制剂(纳米白蛋白紫杉醇)现已在中国上市(商品名:Abraxane(®))。为向主要利益相关者提供卫生经济学数据,开展了一项成本效用分析,比较纳米白蛋白紫杉醇与多西他赛作为紫杉醇替代方案的情况。
进行了一项荟萃分析,纳入比较纳米白蛋白紫杉醇(260mg/m²,每3周一次)或原研多西他赛(100mg/m²,每3周一次)与溶剂型原研紫杉醇(175mg/m²,每3周一次)的III期临床试验的临床结果,以提供安全性和临床数据。从在中国三个癌症中心进行的一项时间动作研究以及对临床医生的一项调查中收集了抗癌治疗及3/4级毒性治疗的资源使用数据。采用时间权衡技术,通过对来自中国一个癌症中心的28例乳腺癌患者进行访谈得出健康效用估计值。所有成本均以2014年美元报告。
纳米白蛋白紫杉醇具有最有利的安全性,其特征为3/4级中性粒细胞减少、发热性中性粒细胞减少、贫血和口腔炎的发生率最低。当应用临床试验中的中位给药周期数时,纳米白蛋白紫杉醇每疗程成本为19,752美元,而紫杉醇和多西他赛分别为8,940美元和13,741美元。作为紫杉醇的替代方案,纳米白蛋白紫杉醇每获得一个质量调整生命年(QALY)的成本表明其价值优于多西他赛(57,900美元对130,600美元)。
在中国,对于转移性乳腺癌,与多西他赛和紫杉醇相比,纳米白蛋白紫杉醇似乎是一种具有成本效益的选择。