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中国抗肿瘤产品仿制药上市影响的中断时间序列分析

Interrupted time-series analysis of the impact of generic market entry of antineoplastic products in China.

作者信息

Guan Xiaodong, Tian Ye, Ross-Degnan Dennis, Man Chunxia, Shi Luwen

机构信息

Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University, Beijing, China.

International Research Center for Medicinal Administration, Peking University, Beijing, China.

出版信息

BMJ Open. 2018 Jul 16;8(7):e022328. doi: 10.1136/bmjopen-2018-022328.

Abstract

OBJECTIVES

The rapid growth of pharmaceutical costs is a major healthcare issue all over the world. The high prices of new drugs, especially those for cancer, are also a concern for stakeholders. Generic drugs are a major price-reducing opportunity and provide more societal value. The aim of this research is to analyse the impact of generic entry on the volume and cost of antineoplastic agents in China.

METHODS

An interrupted time-series design examined monthly sales of three antineoplastic drugs (capecitabine, decitabine, imatinib) from 699 public hospitals during January 2011 to June 2016. The first generic entry times (December 2013, December 2012, August 2013, respectively) were regarded as the intervention time points. We estimated changes in volume and cost following the generic entry.

RESULTS

We found that generic entry was associated with increases in the volume of three antineoplastic agents and decreases in their costs. In terms of volume, generic entry was associated with increases in use of capecitabine, decitabine and imatinib by 815.0 (95% CI -66.5 to 1696.5, p>0.05), 11.0 (95% CI 3.7 to 18.3, p=0.004) and 2145.5 (95% CI 1784.1 to 2506.9, p<0.001) units. The entry of generic antineoplastic drugs reduced the monthly cost trend of three agents by ¥3.1 (95% CI -¥3.6 to -¥2.6, p<0.001), ¥84.7 (95% CI -¥104.7 to -¥64.6, p<0.001) and ¥21.3 (95% CI -¥24.2 to -¥18.4, p<0.001), respectively. The entry of generic drugs attenuated the upward trend in volume of three brand-name drugs and even triggered reductions in the volume of brand-name capecitabine. The entry of generics was accompanied by significant increase of ¥2.6 in monthly brand-name decitabine cost (95% CI ¥0.2 to ¥5.1, p=0.04).

CONCLUSION

Our findings suggested that entry of generic drugs impacted use and cost of antineoplastic medicines in China. Generic drugs may improve the availability and the affordability of antineoplastic agents, which would benefit more patients.

摘要

目的

药品成本的快速增长是全球主要的医疗保健问题。新药价格高昂,尤其是癌症药物,这也引起了利益相关者的关注。仿制药是一个主要的降价机会,能提供更多的社会价值。本研究旨在分析仿制药进入市场对中国抗肿瘤药物销量和成本的影响。

方法

采用中断时间序列设计,研究了2011年1月至2016年6月期间699家公立医院三种抗肿瘤药物(卡培他滨、地西他滨、伊马替尼)的月度销售情况。将首批仿制药进入市场的时间(分别为2013年12月、2012年12月、2013年8月)视为干预时间点。我们估计了仿制药进入市场后销量和成本的变化。

结果

我们发现,仿制药进入市场与三种抗肿瘤药物的销量增加和成本降低有关。在销量方面,仿制药进入市场后,卡培他滨、地西他滨和伊马替尼的使用量分别增加了815.0(95%置信区间为-66.5至1696.5,p>0.05)、11.0(95%置信区间为3.7至18.3,p=0.004)和2145.5(95%置信区间为1784.1至2506.9,p<0.001)单位。仿制药进入市场后,三种药物的月度成本趋势分别降低了3.1元(95%置信区间为-3.6元至-2.6元,p<0.001)、84.7元(95%置信区间为-104.7元至-64.6元,p<0.001)和21.3元(95%置信区间为-24.2元至-18.4元,p<0.001)。仿制药的进入减弱了三种名牌药物销量的上升趋势,甚至导致名牌卡培他滨销量下降。仿制药进入市场后,名牌地西他滨的月度成本显著增加了2.6元(95%置信区间为0.2元至5.1元,p=0.04)。

结论

我们的研究结果表明,仿制药进入市场对中国抗肿瘤药物的使用和成本产生了影响。仿制药可能会提高抗肿瘤药物的可及性和可负担性,从而使更多患者受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08f/6082476/d3cdfef0127e/bmjopen-2018-022328f01.jpg

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