RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The role of Shenqi Fuzheng injection as adjuvant therapy for breast cancer: an overview of systematic reviews and meta-analyses.
The role of Shenqi Fuzheng injection as adjuvant therapy for breast cancer: an overview of systematic reviews and meta-analyses.
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对于 BC,辅助 CT 联合 SFI 具有更好的获益和更低的不良事件风险。
乳腺癌(BC)是全球最常见的恶性肿瘤。化疗(CT)是乳腺癌常用治疗,但伴随毒性和不良反应。临床研究显示,参芪扶正注射液(SFI)作为辅助治疗具有提高疗效、减轻毒性的潜力。本系统综述和荟萃分析(SR/MA)概述SFI辅助化疗治疗乳腺癌的获益,并评估相关证据质量。
系统检索PubMed、Web of Science、EMbase、Cochrane Library、CNKI、万方、维普和SinoMed数据库自建库至2022年10月1日发表的SFI治疗乳腺癌随机对照试验(RCT)系统综述/荟萃分析。由两名评审者使用AMSTAR-2、PRISMA 2020、ROBIS和GRADE评估综述质量。使用校正后的覆盖面积(CCA)量化原始SR/MA的重复程度。最后,使用RevMan 5.4软件对RCT开展定量分析。本研究在PROSPERO注册,编号CRD42022377290。
纳入6篇SR/MA,涵盖61项RCT和5593名患者。研究发表于2015至2019年,原始RCT数量为7至49项,样本量为336至1989人。定量荟萃分析发现,SFI辅助化疗提高了乳腺癌患者的临床缓解率(RR=1.37,95% CI=1.28至1.46;P<0.00001)和KPS评分(RR=1.66,95% CI=1.54至1.79;P<0.00001)。在免疫功能方面,SFI辅助化疗组的CD3+(SMD=1.51,95% CI=0.91至2.10;P<0.00001)、CD4+(SMD=1.87,95% CI=1.18至2.56;P<0.00001)、CD4+/CD8+(SMD=0.86,95% CI=0.48至1.23;P<0.00001)及NK细胞水平(SMD=0.94,95% CI=0.63至1.24;P<0.00001)均优于单纯化疗组。SFI辅助化疗后,白细胞减少(RR=0.53,95% CI=0.46至0.62;P<0.00001)和胃肠道反应(RR=0.48,95% CI=0.39至0.58;P<0.00001)的发生率降低。然而,GRADE显示42项结局的证据质量从“极低”到“中等”不等,没有高质量证据支持,主要受RCT设计缺陷(42/42,100%)、不一致性(19/42,45.24%)、发表偏倚(41/42,97.62%)和不精确性(3/42,7.14%)限制。AMSTAR-2、PRISMA 2020和ROBIS评估结果不理想,问题包括未注册研究方案、未说明纳入RCT依据、未描述纳入研究的资金来源、检索策略及筛选过程不完整、未处理异质性和敏感性分析,以及未报告潜在利益冲突。
SFI辅助化疗治疗乳腺癌可能获益更多且不良事件风险较低。但方法学和证据质量总体偏低,研究实施中需给予更多重视。临床决策仍需更客观、高质量的研究验证SFI疗效。
Breast cancer (BC) is the most frequent malignancy in the world. Chemotherapy (CT) is a common treatment for BC but is accompanied by toxicity and side effects. Shenqi Fuzheng Injection (SFI) is an adjuvant therapy with promising results in improving efficacy and reducing toxicity in clinical studies. This overview of systematic reviews and meta-analysis (SRs/MAs) aimed to summarize the benefits and evaluate the quality of evidence supporting SFI adjuvant as CT for BC.
A systematic search for SRs/MAs of randomized controlled trials (RCTs) on SFI treatment for BC was performed by searching PubMed, Web of Science, EMbase, Cochrane Library, CNKI, Wanfang, VIP, and SinoMed databases from inception to October 1, 2022. The quality of SRs/MAs was evaluated using AMSTAR-2, PRISMA 2020, ROBIS, and GRADE by two reviewers. The corrected covered area (CCA) was used to quantify the degree of duplication of the original SRs/MAs. Finally, quantitative analysis of RCTs was conducted using RevMan 5.4 software. This study was registered with PROSPERO, CRD42022377290.
Six SRs/MAs including 61 RCTs with 5593 patients were included in this study. Studies were published between 2015 and 2019, the original RCTs ranged from 7-49, with sample sizes ranging from 336-1989. The quantitative meta-analysis found that adjuvant CT of SFI improved the clinical response rate (RR=1.37, 95% CI=1.28, 1.46; P<0.00001) and the KPS score (RR=1.66, 95% CI 1.54, 1.79, P<0.00001) of patients with BC. In terms of immune function, CD3+ (SMD=1.51, 95% CI 0.91, 2.10; P<0.00001), CD4+ (SMD=1.87, 95% CI 1.18, 2.56; P<0.00001), CD4+/CD8+ (SMD=0.86, 95% CI 0.48, 1.23; P<0.00001), and NK cell levels (SMD=0.94, 95% CI 0.63, 1.24; P<0.00001) in the adjuvant CT group SFI were better than those with CT alone. Adverse reactions following SFI adjuvant CT showed reduced incidence of leukopenia (RR=0.53, 95% CI 0.46, 0.62; P<0.00001) and gastrointestinal reactions (RR=0.48, 95% CI 0.39, 0.58; P<0.00001). However, the GRADE results showed 'very low' to 'moderate' evidence for the 42 outcomes, without high-quality evidence supporting them, limited mainly by deficiencies in the design of RCTs (42/42, 100.00%), inconsistency (19/42, 45.24%), publication bias (41/42, 97.62%), and inaccuracy (3/42, 7.14%). The unsatisfactory results of AMSTAR-2, PRISMA 2020, and ROBIS were limited to lack of registration of study protocols, explanation of inclusion basis of RCTs, description of funding sources for the included studies, incomplete search strategy and screening process, addressing heterogeneity and sensitivity, and reporting potential conflicts of interest.
Adjuvant CT with SFI for BC had better benefits and a lower risk of adverse events. The methodology and quality of the evidence are generally low, highlighting a need of greater attention during study implementation. More objective and high-quality studies are needed to verify the efficacy of adjuvant CT with SFI in clinical decision-making for BC.
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