Konstantis Georgios, Tsaousi Georgia, Pourzitaki Chryssa, Kitsikidou Elisavet, Magouliotis Dimitrios E, Wiener Sebastian, Zeller Amos Cornelius, Willuweit Katharina, Schmidt Hartmut H, Rashidi-Alavijeh Jassin
Clinical Pharmacology, Faculty of Medicine, School of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Department of Gastroenterology, Hepatology and Transplant Medicine, Medical Faculty, University of Duisburg-Essen, 40219 Essen, Germany.
J Clin Med. 2023 Oct 16;12(20):6541. doi: 10.3390/jcm12206541.
Acute-on-chronic liver failure (ACLF) mostly occurs when there is an acute insult to the liver in patients with pre-existing liver disease, and it is characterized by a high mortality rate. Various therapeutic approaches have been used thus far, with orthotopic liver transplantation being the only definitive cure. Clinical trials and meta-analyses have investigated the use of granulocyte colony-stimulating factor (G-CSF) to mobilize bone marrow-derived stem cells. Some studies have suggested that G-CSF may have a significant role in the management and survival of patients with ACLF. However, the results are conflicting, and the efficacy of G-CSF still needs to be confirmed.
The aim was to assess the efficacy of G-CSF in patients with ACLF.
Electronic databases were searched until May 2023 for randomized controlled trials investigating the use of G-CSF in adult patients with ACLF. Outcome measures were the effects of G-CSF on overall survival, changes in liver disease severity scores, complications of cirrhosis, other G-CSF-related adverse effects, and all-cause mortality. The study's protocol has been registered with Prospero (CRD42023420273).
Five double-blind randomized controlled trials involving a total of 421 participants met the inclusion criteria. The use of G-CSF demonstrated a significant effect on overall survival (HR 0.63, 95% CI 0.41 to 0.95, and I 48%), leading to a decreased mortality (LogOR-0.97, 95% CI -1.57 to -0.37, and I 37.6%) and improved Model for End-Stage Liver Disease (MELD) scores (SMD -0.87, 95% CI -1.62 to -0.13, and I 87.3%). There was no correlation between the improvement of the Child-Pugh score and the use of G-CSF(SMD -2.47, 95% CI -5.78 to 0.83, and I 98.1%). The incidence of complications of cirrhosis did not decrease significantly with G-CSF treatment (rate ratio 0.51, 95% CI 0.26 to 1.01, and I 90%). A qualitative synthesis showed that the use of G-CSF is safe.
The administration of G-CSF has demonstrated a positive impact on overall survival, liver function, and the MELD score. The presence of heterogeneity in the included studies prohibits conclusive recommendations.
慢加急性肝衰竭(ACLF)多发生于已有肝病的患者肝脏受到急性损伤时,其特点是死亡率高。迄今为止已采用了多种治疗方法,原位肝移植是唯一的根治方法。临床试验和荟萃分析研究了使用粒细胞集落刺激因子(G-CSF)动员骨髓来源干细胞的情况。一些研究表明,G-CSF可能在ACLF患者的管理和生存中发挥重要作用。然而,结果相互矛盾,G-CSF的疗效仍需证实。
评估G-CSF对ACLF患者的疗效。
检索电子数据库至2023年5月,以查找调查G-CSF在成年ACLF患者中应用的随机对照试验。观察指标为G-CSF对总生存期、肝病严重程度评分变化、肝硬化并发症、其他与G-CSF相关的不良反应以及全因死亡率的影响。该研究方案已在国际前瞻性系统评价注册库(CRD42023420273)注册。
五项双盲随机对照试验共纳入421名参与者,符合纳入标准。使用G-CSF对总生存期有显著影响(风险比0.63,95%置信区间0.41至0.95,I² 48%),导致死亡率降低(对数比值比-0.97,95%置信区间-1.57至-0.37,I² 37.6%),终末期肝病模型(MELD)评分改善(标准化均数差-0.87,95%置信区间-1.62至-0.13,I² 87.3%)。Child-Pugh评分的改善与G-CSF的使用之间无相关性(标准化均数差-2.47,95%置信区间-5.78至0.83,I² 98.1%)。G-CSF治疗并未使肝硬化并发症的发生率显著降低(率比0.51,95%置信区间0.26至1.01,I² 90%)。定性综合分析表明,使用G-CSF是安全的。
G-CSF的应用已证明对总生存期、肝功能和MELD评分有积极影响。纳入研究中存在异质性,无法给出确定性建议。