Endocrine therapies in postmenopausal women with hormone receptor-positive, human epidermal growth factor receptor 2-negative, pretreated, advanced breast cancer A network meta-analysis

被引:3
|
作者
Lee, Cho-Hao [1 ]
Kang, Yi-No [2 ]
Ho, Ching-Liang [1 ]
Lin, Chin [3 ,4 ]
Chen, Po-Huang [1 ]
Wu, Yi-Ying [1 ]
Huang, Tzu-Chuan [1 ]
机构
[1] Triserv Gen Hosp, Natl Def Med Ctr, Dept Internal Med, Div Hematol & Oncol Med, 325,Sec 2,Chenggong Rd, Taipei 114, Taiwan
[2] Taipei Med Univ Hosp, Dept Educ, Ctr Evidence Based Med, Taipei, Taiwan
[3] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[4] Natl Def Med Ctr, Sch Publ Hlth, Taipei, Taiwan
关键词
breast cancer; endocrine therapy; hormone receptor; hormone therapy; network meta-analysis; EVEROLIMUS PLUS EXEMESTANE; PALBOCICLIB; CHEMOTHERAPY; HEALTH; MULTICENTER; FULVESTRANT; RIBOCICLIB; GUIDANCE; SAFETY;
D O I
10.1097/MD.0000000000019618
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Recently, many endocrine therapies have become available for hormone receptor-positive, human epidermal growth factor receptor 2-negative, pretreated, advanced breast cancer. Direct comparisons of these novel treatments to assess their added value, however, are lacking Methods: Our aim was to synthesize available evidence to compare all current endocrine treatments for hormone receptor-positive / human epidermal growth factor receptor 2-negative advanced breast cancer. We performed a systematic review to identify available randomized controlled trial evidence. We searched Embase, MEDLINE, and the Cochrane Central Register of Controlled Clinical Trials. Two trials presented at international oncology congresses (American Society of Clinical Oncology [ASCO]) were added to include the most recent evidence. A frequent network meta-analysis was used, and the surface under cumulative ranking area (SUCRA) was calculated to determine the best treatment Results: In total, 32 trials and 12,726 patients were identified, including 27 arms. Compared with fulvestrant 500 mg alone, novel target inhibitors combined with fulvestrant or exemestane had significantly prolonged progression-free survival with hazard ratios ranging from 0.62 to 0.82. Fulvestrant 500 mg plus palbociclib 125 mg and exemestane 25 mg plus entinostat 5 mg similarly extended progression-free survival (hazard ratio: 0.64 and 0.62 with SUCRA values of 91% and 92%, respectively). The exemestane 25 mg plus everolimus 10 mg combination had the best clinical benefit rate (risk ratio: 1.84, SUCRA: 91%) and overall response rate (risk ratio: 6.05, SUCRA: 97%) Conclusions: On the basis of this analysis, the 2 combinations of exemestane plus everolimus and fulvestrant plus palbociclib were the best treatment options
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页数:10
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