Interunit Graduate Program in Biotechnology (PPIB), University of São Paulo - USP, Sãu Paulo, Brazil.
Industrial Biotechnology Laboratory (LBI), Institute of Technological Research of São Paulo - IPT, Sãu Paulo, Brazil.
J Oncol Pharm Pract. 2023 Oct;29(7):1736-1747. doi: 10.1177/10781552231190104. Epub 2023 Jul 28.
We conducted a systematic review and meta-analysis aiming to assess the efficacy and safety of Nivolumab treatment in patients with newly diagnosed and recurrent glioblastoma multiforme (GBM).
Our study followed the guidelines outlined in the preferred reporting items for systematic reviews and meta-analyses (PRISMA) recommendations. The protocol for this review can be found in the International Prospective Register of Systematic Reviews Database (CRD42022340071). We performed searches on the Medline, PubMed, Embase, Scopus, and Web of Science databases.
A total of 545 studies were identified through our comprehensive search across the five databases (PubMed: 78, Embase: 82, Medline: 173, Scopus: 138, Web of Science: 74). After conducting a thorough analysis, our meta-analysis indicated that treatment with Nivolumab led to improved overall survival (OS) outcomes in newly diagnosed glioblastoma patients, as evidenced by a prolonged median OS based on trial data. However, there was no significant beneficial effect observed in terms of median progression-free survival (PFS), as well as OS at 6, 12, and 24 months. Furthermore, our results demonstrated no efficacy of Nivolumab in the treatment of recurrent GBM patients.
In conclusion, Nivolumab demonstrated promising results that warrant further investigation for its use in newly diagnosed glioblastoma patients. However, its effectiveness was not observed in the context of recurrent GBM.
我们进行了一项系统评价和荟萃分析,旨在评估纳武利尤单抗治疗新诊断和复发性多形性胶质母细胞瘤(GBM)患者的疗效和安全性。
我们的研究遵循系统评价和荟萃分析首选报告项目(PRISMA)建议中的指南。本综述的方案可在国际前瞻性注册系统评价数据库(CRD42022340071)中找到。我们在 Medline、PubMed、Embase、Scopus 和 Web of Science 数据库中进行了搜索。
通过对这五个数据库的全面搜索,共确定了 545 项研究(PubMed:78 项,Embase:82 项,Medline:173 项,Scopus:138 项,Web of Science:74 项)。经过彻底分析,我们的荟萃分析表明,纳武利尤单抗治疗新诊断的胶质母细胞瘤患者可改善总体生存(OS)结局,这是基于试验数据得出的延长中位 OS 所证明的。然而,在中位无进展生存期(PFS)以及 6、12 和 24 个月时的 OS 方面,并没有观察到显著的有益效果。此外,我们的结果表明纳武利尤单抗在复发性 GBM 患者的治疗中无效。
总之,纳武利尤单抗显示出有前途的结果,值得进一步研究其在新诊断的胶质母细胞瘤患者中的应用。然而,在复发性 GBM 中未观察到其有效性。