Xia Guangfa, Zhang Ziran, Jing Sili, Liu Wanyin
Department of Breast Diseases, Jiaxing Maternity and Child Health Care Hospital, Affiliated Women and Children's Hospital of Jiaxing University 2468 Central East Road, Jiaxing 314000, Zhejiang, P. R. China.
Am J Transl Res. 2024 Sep 15;16(9):5049-5062. doi: 10.62347/ZXWY3004. eCollection 2024.
This study used meta-analysis to examine the role of baseline absolute lymphocyte count (ALC) in the prognosis of advanced breast cancer (ABC) or metastatic breast cancer (MBC). A comprehensive search encompassing PubMed, The Cochrane Library, Embase, and Web of Science databases was undertaken to identify and screen literature based on predefined inclusion and exclusion criteria. Progression-free survival (PFS), time to treatment failure (TTF), post-progression survival (PPS), and overall survival (OS) were selected as outcome measures. A meta-analysis of 14 studies, involving 2,540 patients and employing Review Manager 5.3 and Stata 14.0, was conducted. Notably, 12 of these studies originated from Japan. The findings indicated that patients with ABC or MBC exhibiting high ALC had significantly improved PFS, TTF, PPS (hazard ratio [HR] = 0.53, 95% confidence interval [CI]: 0.45-0.62, < 0.00001; HR = 0.57, 95% CI: 0.51-0.64, < 0.00001), and OS (HR = 0.44, 95% CI: 0.33-0.58, < 0.00001; HR = 0.68, 95% CI: 0.60-0.77, < 0.00001) juxtaposed with low ALC individuals. These findings were corroborated by both univariate and multivariate analyses. Furthermore, subgroup analysis based on breast cancer subtype unveiled that high ALC was associated with prolonged PFS (HR = 0.35, 95% CI: 0.21-0.56, < 0.0001), TTF, and PPS (HR = 0.45, 95% CI: 0.29-0.71, = 0.0006) in both human epidermal growth factor receptor 2 (HER-2)-positive and -negative ABC or MBC patients. Additionally, high ALC correlated with prolonged OS in all BC subtypes (HR = 0.73, 95% CI: 0.61-0.88, P = 0.0008) and HER-2-negative ABC or MBC patients (HR = 0.65, 95% CI: 0.55-0.78, P < 0.00001). Subgroup analysis was conducted on chemotherapy regimens, with and without eribulin. Despite variations in chemotherapy regimens, patients with ABC or MBC and high ALC exhibited longer PFS and PPS (HR = 0.45, 95% CI: 0.30-0.67, < 0.0001), PFS and TTF (HR = 0.39, 95% CI: 0.20-0.78, = 0.008), and OS (HR = 0.71, 95% CI: 0.62-0.82, < 0.00001; HR = 0.5, 95% CI: 0.35-0.70, < 0.0001). The results of this meta-analysis suggest that baseline ALC, as an immune marker, can serve as an effective prognostic indicator for ABC or MBC.
本研究采用荟萃分析来探讨基线绝对淋巴细胞计数(ALC)在晚期乳腺癌(ABC)或转移性乳腺癌(MBC)预后中的作用。我们全面检索了PubMed、Cochrane图书馆、Embase和Web of Science数据库,根据预先设定的纳入和排除标准来识别和筛选文献。无进展生存期(PFS)、治疗失败时间(TTF)、进展后生存期(PPS)和总生存期(OS)被选为结局指标。我们对14项研究进行了荟萃分析,涉及2540例患者,并使用Review Manager 5.3和Stata 14.0软件进行分析。值得注意的是,其中12项研究来自日本。研究结果表明,ABC或MBC患者中ALC高者的PFS、TTF、PPS(风险比[HR]=0.53,95%置信区间[CI]:0.45 - 0.62,P<0.00001;HR = 0.57,95% CI:0.51 - 0.64,P<0.00001)和OS(HR = 0.44,95% CI:0.33 - 0.58,P<0.00001;HR = 0.68,95% CI:0.60 - 0.77,P<0.00001)与ALC低者相比均有显著改善。单因素和多因素分析均证实了这些结果。此外,基于乳腺癌亚型的亚组分析表明,在人表皮生长因子受体2(HER-2)阳性和阴性的ABC或MBC患者中,高ALC与更长的PFS(HR = 0.35,95% CI:0.21 - 0.56,P<0.0001)、TTF和PPS(HR = 0.45,95% CI:0.29 - 0.71,P = 0.0006)相关。此外,在所有乳腺癌亚型中高ALC与更长的OS相关(HR = 0.73,95% CI:0.61 - 0.88,P = 0.0008),在HER-2阴性的ABC或MBC患者中也是如此(HR = 0.65,95% CI:0.55 - 0.78,P<0.00001)。我们对含和不含艾日布林的化疗方案进行了亚组分析。尽管化疗方案存在差异,但ABC或MBC且ALC高的患者表现出更长的PFS和PPS(HR = 0.45,95% CI:0.30 - 0.67,P<0.0001)、PFS和TTF(HR = 0.39,95% CI:0.20 - 0.78,P = 0.008)以及OS(HR = 0.71,95% CI:0.62 - 0.82,P<0.00001;HR = 0.5,95% CI:0.35 - 0.70,P<0.0