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卡培他滨在接受标准化疗的早期三阴性乳腺癌患者中的额外应用:新时代?一项随机对照试验的荟萃分析。

Additional capecitabine use in early-stage triple negative breast cancer patients receiving standard chemotherapy: a new era? A meta-analysis of randomized controlled trials.

机构信息

Department of Breast Oncology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 East Dongfeng Road, Guangzhou, Guangzhou, 510060, Guangdong, China.

Department of Breast Oncology, Guangdong Hospital of Traditional Chinese Medicine, Guangzhou, Guangdong, China.

出版信息

BMC Cancer. 2022 Mar 12;22(1):261. doi: 10.1186/s12885-022-09326-5.

Abstract

BACKGROUND

The efficiency of capecitabine has been proven in early-stage triple negative breast cancer (eTNBC) with residue invasive tumor (non-pCR) after standard neoadjuvant chemotherapy (NACT). However, for those unselected eTNBC patients without screening from NACT (i.e., newly diagnosed eTNBC patients undergoing breast surgery followed by adjuvant systemic therapy), the value of capecitabine has still remains unclear. We performed a meta-analysis of randomized controlled trials (RCTs) to evaluate whether additional capecitabine in eTNBC patients could improve clinical outcomes.

METHODS

Seven RCTs (USO 01062, FinXX, GEICAM/2003, CREATE-X, CIBOMA/2004, CBCSG-010 and SYSUCC-001) were identified in online databases until December 2020 and included in the meta-analysis. We extracted the survival data including disease/relapse-free survival (DFS/RFS) and overall survival (OS), and utilized the STATA software to calculate the summarized hazard ratios (HRs) and 95% confidence intervals (95%CIs).

RESULTS

A total of 3329 eTNBC patients were enrolled in this meta-analysis, with 1640 receiving standard neo-/adjuvant chemo-regimes alone, and the other 1689 receiving an additional capecitabine use, respectively. Both DFS and OS were significantly improved with the addition of capecitabine, and the benefits remained consistent in those unselected eTNBC patients without screening from NACT. Subgroup analysis further proved that this improvement in DFS was significant in both nodal negative and positive patients. Similar benefits are also found across menopausal status (both pre- and post-menopause). Regarding toxicity, the hand-foot syndrome and neutropenia are the most common capecitabine related adverse events, and are mostly tolerable.

CONCLUSIONS

The present meta-analysis of RCTs demonstrates for the first time that adding capecitabine to standard chemo-regimens could improve both DFS and OS in unselected eTNBC patients, and this benefit remains consistent regardless of nodal status and menopausal status, which may lead eTNBC therapy into a new era.

摘要

背景

卡培他滨在标准新辅助化疗(NACT)后残留浸润性肿瘤(非 pCR)的早期三阴性乳腺癌(eTNBC)中已被证明有效。然而,对于那些未经 NACT 筛选的未选择的 eTNBC 患者(即新诊断的 eTNBC 患者接受乳房手术后接受辅助全身治疗),卡培他滨的价值仍不清楚。我们对随机对照试验(RCT)进行了荟萃分析,以评估在 eTNBC 患者中添加卡培他滨是否可以改善临床结局。

方法

直到 2020 年 12 月,我们在在线数据库中确定了 7 项 RCT(USO 01062、FinXX、GEICAM/2003、CREATE-X、CIBOMA/2004、CBCSG-010 和 SYSUCC-001)并将其纳入荟萃分析。我们提取了包括疾病/无病生存(DFS/RFS)和总生存(OS)在内的生存数据,并使用 STATA 软件计算了汇总的风险比(HR)和 95%置信区间(95%CI)。

结果

共有 3329 名 eTNBC 患者纳入本荟萃分析,其中 1640 名患者接受标准新辅助/辅助化疗方案单独治疗,另外 1689 名患者接受卡培他滨联合治疗。DFS 和 OS 均显著改善,在未经 NACT 筛选的未选择的 eTNBC 患者中也保持一致。亚组分析进一步证明,DFS 的改善在淋巴结阴性和阳性患者中均有统计学意义。在绝经前和绝经后患者中也发现了类似的益处。关于毒性,手足综合征和中性粒细胞减少症是最常见的卡培他滨相关不良事件,且大多可耐受。

结论

本 RCT 荟萃分析首次表明,在标准化疗方案中添加卡培他滨可改善未经选择的 eTNBC 患者的 DFS 和 OS,并且这种获益与淋巴结状态和绝经状态无关,这可能使 eTNBC 治疗进入一个新时代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccf8/8917675/c4d1a4b245ef/12885_2022_9326_Fig1_HTML.jpg

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