Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, 3-8-22 Honkomagome, Bunkyo-Ku, Tokyo, 113-8677, Japan.
Department of Hemato-Oncology, Saitama Medical University International Medical Center, Saitama, Japan.
Int J Clin Oncol. 2024 Jul;29(7):899-910. doi: 10.1007/s10147-023-02461-4. Epub 2024 May 17.
The outcomes of relapsed or refractory acute myeloid leukemia (AML) remain poor. Although the concomitant use of granulocyte colony-stimulating factor (G-CSF) and anti-chemotherapeutic agents has been investigated to improve the antileukemic effect on AML, its usefulness remains controversial. This study aimed to investigate the effects of G-CSF priming as a remission induction therapy or salvage chemotherapy.
We performed a thorough literature search for studies related to the priming effect of G-CSF using PubMed, Ichushi-Web, and the Cochrane Library. A qualitative analysis of the pooled data was performed, and risk ratios (RRs) with confidence intervals (CIs) were calculated and summarized.
Two reviewers independently extracted and accessed the 278 records identified during the initial screening, and 62 full-text articles were assessed for eligibility in second screening. Eleven studies were included in the qualitative analysis and 10 in the meta-analysis. A systematic review revealed that priming with G-CSF did not correlate with an improvement in response rate and overall survival (OS). The result of the meta-analysis revealed the tendency for lower relapse rate in the G-CSF priming groups without inter-study heterogeneity [RR, 0.91 (95% CI 0.82-1.01), p = 0.08; I = 4%, p = 0.35]. In specific populations, including patients with intermediate cytogenetic risk and those receiving high-dose cytarabine, the G-CSF priming regimen prolonged OS.
G-CSF priming in combination with intensive remission induction treatment is not universally effective in patients with AML. Further studies are required to identify the patient cohort for which G-CSF priming is recommended.
复发或难治性急性髓系白血病(AML)的预后仍然较差。尽管已经研究了粒细胞集落刺激因子(G-CSF)与化疗药物同时使用以提高对 AML 的抗白血病作用,但其有效性仍存在争议。本研究旨在探讨 G-CSF 诱导缓解治疗或挽救性化疗的作用。
我们使用 PubMed、Ichushi-Web 和 Cochrane Library 对与 G-CSF 诱导作用相关的研究进行了全面的文献检索。对汇总数据进行了定性分析,并计算和总结了风险比(RR)及其置信区间(CI)。
两名审查员独立提取并评估了初次筛选中确定的 278 条记录,并对第二轮筛选中的 62 篇全文文章进行了资格评估。11 项研究纳入了定性分析,10 项研究纳入了荟萃分析。系统评价显示,G-CSF 诱导缓解与缓解率和总生存(OS)的改善无关。荟萃分析的结果表明,G-CSF 诱导缓解组的复发率较低,且无研究间异质性[RR,0.91(95% CI 0.82-1.01),p=0.08;I=4%,p=0.35]。在特定人群中,包括具有中间细胞遗传学风险的患者和接受高剂量阿糖胞苷治疗的患者,G-CSF 诱导缓解方案延长了 OS。
在 AML 患者中,G-CSF 诱导缓解联合强化缓解诱导治疗并非普遍有效。需要进一步研究以确定推荐 G-CSF 诱导缓解的患者人群。