HER2-targeted therapy prolongs survival in patients with HER2-positive breast cancer and intracranial metastatic disease: a systematic review and meta-analysis.
HER2-targeted therapy prolongs survival in patients with HER2-positive breast cancer and intracranial metastatic disease: a systematic review and meta-analysis.
复制标题
DOI:
10.1093/noajnl/vdaa136
复制
发表时间:
2020-01
期刊:
影响因子:
--
通讯作者:
Das S
中科院分区:
文献类型:
--
作者:
Erickson AW;Ghodrati F;Habbous S;Jerzak KJ;Sahgal A;Ahluwalia MS;Das S
Intracranial metastatic disease (IMD) is a serious and known complication of human epidermal growth factor receptor 2 (HER2)-positive breast cancer. The role of targeted therapy for patients with HER2-positive breast cancer and IMD remains unclear. In this study, we sought to evaluate the effect of HER2-targeted therapy on IMD from HER2-positive breast cancer. We searched MEDLINE, EMBASE, CENTRAL, and gray literature sources for interventional and observational studies reporting survival, response, and safety outcomes for patients with IMD receiving HER2-targeted therapy. We pooled outcomes through meta-analysis and examined confounder effects through forest plot stratification and meta-regression. Evidence quality was evaluated using GRADE (PROSPERO CRD42020161209). A total of 97 studies (37 interventional and 60 observational) were included. HER2-targeted therapy was associated with prolonged overall survival (hazard ratio [HR] 0.47; 95% confidence interval [CI], 0.39–0.56) without significantly prolonged progression-free survival (HR 0.52; 95% CI, 0.27–1.02) versus non-targeted therapy; the intracranial objective response rate was 19% (95% CI, 12–27%), intracranial disease control rate 62% (95% CI, 55–69%), intracranial complete response rate 0% (95% CI, 0–0.01%), and grade 3+ adverse event rate 26% (95% CI, 11–45%). Risk of bias was high in 40% (39/97) of studies. These findings support a potential role for systemic HER2-targeted therapy in the treatment of patients with IMD from HER2-positive metastatic breast cancer.
登录
查看更多内容
影响因子:
3.8
作者:
Bartsch R;De Vries C;Pluschnig U;Dubsky P;Bago-Horvath Z;Gampenrieder SP;Rudas M;Mader RM;Rottenfusser A;Wiltschke C;Gnant M;Zielinski CC;Steger GG
通讯作者:
Steger GG
影响因子:
8.4
作者:
Bonneau, Claire;Paintaud, Gilles;Gutierrez, Maya
通讯作者:
Gutierrez, Maya
影响因子:
28.4
作者:
Borges, Virginia F.;Ferrario, Cristiano;Hamilton, Erika
通讯作者:
Hamilton, Erika
影响因子:
50.5
作者:
de Azambuja, E.;Zardavas, D.;Awada, A.
通讯作者:
Awada, A.
影响因子:
51.1
作者:
Bachelot, Thomas;Romieu, Gilles;Labbe-Devilliers, Catherine
通讯作者:
Labbe-Devilliers, Catherine