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免疫检查点抑制剂联合新辅助化疗治疗早期三阴性乳腺癌:系统评价和荟萃分析。

Immune checkpoint inhibitors plus neoadjuvant chemotherapy in early triple-negative breast cancer: a systematic review and meta-analysis.

机构信息

Breast Disease Diagnosis and Treatment Center of Affiliated Hospital of Qinghai University & Affiliated Cancer Hospital of Qinghai University, Xining, 810000, China.

出版信息

BMC Cancer. 2021 Nov 23;21(1):1261. doi: 10.1186/s12885-021-08997-w.

Abstract

PURPOSE

Some studies have shown that Immune checkpoint inhibitors (ICIs) have a favorable efficacy in advanced triple negative breast cancer (TNBC) patients, but the results are controversial in neoadjuvant chemotherapy (NACT) stage. The purpose of this study is to evaluate the efficacy and safety after NACT plus ICIs in early TNBC patients.

METHODS

After searching PubMed, EMBASE, the Cochrane library and several mainly oncology conferences up to 30 January 2021 systematically, and define randomized controlled trials (RCTs) exploring the efficacy and safety of programmed death protein-1/programmed cell death-Ligand 1(PD-1/PD-L1) inhibitors plus neoadjuvant chemotherapy in TNBC patients. The primary endpoint was the pathological complete response (pCR) in intention-to-treat populations (ITT), and the secondary endpoints were event-free survival (EFS) and safety analysis in the ITT populations.

RESULTS

Six RCTs (N = 2142) were included in our meta-analysis; NACT plus ICIs increased pCR rates compared with NACT in intention-to-treat (ITT) populations (OR: 1.91; 95% CI: 1.32-2.78, P < 0.001). The pCR rate also increased in both PD-L1 positive (OR: 1.65; 95% CI: 1.26-2.16, P < 0.001) and PD-L1 negative patients (OR: 1.56; 95% CI: 1.04-2.33, P = 0.03), especially in PD-L1 positive patients. The benefit was also observed in nodal-positive populations (OR: 2.52; 95% CI: 1.69-3.77, P < 0.001) and Eastern Cooperative Oncology Group performance-status score (ECOG PS) 0 subgroup (OR: 1.90; 95% CI: 1.42-2.53, P < 0.001). Three RCTs (N = 1615) reported EFS and the results showed that adding PD-1/PD-L1 inhibitors increased EFS (HR 0.65, 95% CI 0.50-0.83, P = 0.0007) in ITT populations with a short follow-up time. In the safety analysis of 2205 patients with early TNBC from five eligible studies, NACT plus ICIs had a higher risk of grade 3-4 diarrhea (OR: 2.54; 95% CI: 1.21-5.32; P = 0.01), any grade of adverse effects(AEs)including vomiting (OR: 1.37; 95% CI: 1.00-1.86; P = 0.05), hyperthyroidism (OR: 6.04; 95% CI: 2.39-15.29; P < 0.001), and hypothyroidism (OR: 5.04; 95% CI: 3.02-8.39; P < 0.001).

CONCLUSIONS

PD-1/PD-L1 inhibitors combined with chemotherapy can improve pCR rates and EFS, and with an increased incidence of some immune-related AEs compared with chemotherapy alone. NACT plus ICIs might be an option in patients with in PD-L1 positive and high-risk populations with positive nodal disease early TNBC.

摘要

目的

一些研究表明,免疫检查点抑制剂(ICI)在晚期三阴性乳腺癌(TNBC)患者中具有良好的疗效,但在新辅助化疗(NACT)阶段的结果存在争议。本研究旨在评估早期 TNBC 患者在 NACT 后加用 ICI 的疗效和安全性。

方法

通过系统检索 PubMed、EMBASE、Cochrane 图书馆和几个主要肿瘤学会议,截至 2021 年 1 月 30 日,定义了探索 PD-1/PD-L1 抑制剂联合新辅助化疗在 TNBC 患者中的疗效和安全性的随机对照试验(RCT)。主要终点为意向治疗人群(ITT)中的病理完全缓解(pCR),次要终点为 ITT 人群中的无事件生存(EFS)和安全性分析。

结果

共有 6 项 RCT(N=2142)纳入我们的荟萃分析;与 NACT 相比,NACT 加 ICI 可提高 ITT 人群中的 pCR 率(OR:1.91;95%CI:1.32-2.78,P<0.001)。在 PD-L1 阳性(OR:1.65;95%CI:1.26-2.16,P<0.001)和 PD-L1 阴性患者(OR:1.56;95%CI:1.04-2.33,P=0.03)中,pCR 率也增加,特别是在 PD-L1 阳性患者中。在淋巴结阳性人群(OR:2.52;95%CI:1.69-3.77,P<0.001)和东部肿瘤协作组体力状况评分(ECOG PS)0 亚组(OR:1.90;95%CI:1.42-2.53,P<0.001)中也观察到了获益。三项 RCT(N=1615)报告了 EFS,结果表明,在 ITT 人群中,与单独使用化疗相比,加用 PD-1/PD-L1 抑制剂可增加 EFS(HR 0.65,95%CI 0.50-0.83,P=0.0007),随访时间较短。在来自五项合格研究的 2205 例早期 TNBC 患者的安全性分析中,NACT 加 ICI 与 3-4 级腹泻(OR:2.54;95%CI:1.21-5.32;P=0.01)、任何级别不良事件(AEs)包括呕吐(OR:1.37;95%CI:1.00-1.86;P=0.05)、甲状腺功能亢进(OR:6.04;95%CI:2.39-15.29;P<0.001)和甲状腺功能减退(OR:5.04;95%CI:3.02-8.39;P<0.001)的风险更高。

结论

PD-1/PD-L1 抑制剂联合化疗可提高 pCR 率和 EFS,与单独化疗相比,免疫相关不良事件(AEs)的发生率增加。在 PD-L1 阳性和高危人群(淋巴结阳性早期 TNBC)中,NACT 加 ICI 可能是一种选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35be/8609839/fdde27ff2c53/12885_2021_8997_Fig1_HTML.jpg

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