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.
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DOI:
10.1093/noajnl/vdaa136
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发表时间:
2020-01
期刊:
Neuro-oncology advances
影响因子:
--
通讯作者:
Das S
Das S
中科院分区:
其他
文献类型:
--
作者:
Erickson AW;Ghodrati F;Habbous S;Jerzak KJ;Sahgal A;Ahluwalia MS;Das S

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颅内转移性疾病 (IMD) 是人类表皮生长因子受体 2 (HER2) 阳性乳腺癌的一种严重且已知的并发症。靶向治疗对于 HER2 阳性乳腺癌和 IMD 患者的作用尚不清楚。在这项研究中,我们试图评估 HER2 靶向治疗对 HER2 阳性乳腺癌 IMD 的效果。我们检索了 MEDLINE、EMBASE、CENTRAL 和灰色文献来源,以查找报告接受 HER2 靶向治疗的 IMD 患者的生存、缓解和安全性结果的干预性和观察性研究。我们通过荟萃分析汇总结果,并通过森林图分层和荟萃回归检查混杂因素的影响。使用 GRADE (PROSPERO CRD42020161209) 评估证据质量。总共纳入 97 项研究(37 项干预性研究和 60 项观察性研究)。与非靶向治疗相比,HER2 靶向治疗可延长总生存期(风险比 [HR] 0.47;95% 置信区间 [CI],0.39–0.56),但无显着延长无进展生存期(HR 0.52;95% CI,0.27–1.02);颅内客观缓解率为19%(95% CI,12-27%),颅内疾病控制率为62%(95% CI,55-69%),颅内完全缓解率为0%(95% CI,0-0.01%),3级以上不良事件发生率为26%(95% CI,11-45%)。 40% (39/97) 的研究存在较高偏倚风险。这些发现支持全身 HER2 靶向治疗在治疗 HER2 阳性转移性乳腺癌 IMD 患者中的潜在作用。
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.
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