Ali Haider Bangash, Prabhat Poudel, Khalid M Alshuqayfi, Mudassir Ahmed, Oluwaseun O Akinduro, Walid Ibn Essayed, Afshin Salehi, Rafael De la Garza Ramos, Reza Yassari, Harminder Singh, Jason P Sheehan, Yoshua Esquenazi
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Data on preclinical models, biochemical mechanisms, and outcomes were extracted and synthesized systrmatically.</p><p><strong>Results: </strong>Out of a total of 7 studies, five preclinical studies met the inclusion criteria. The studies utilized various in vivo mouse models, including bilateral tumor models and immunohumanized mice. Key biochemical mechanisms identified included immunogenic cell death, danger-associated molecular pattern release, macrophage activation, and enhanced T cell responses. Combinatorial approaches involving oncolytic virotherapy, nanoparticle-based treatments, radiation therapy, and immune checkpoint inhibitors showed promise in inducing abscopal effects. Significant tumor growth inhibition and improved survival were reported in treated animals. However, the RAA analysis highlighted concerns regarding research transparency and internal validity across studies.</p><p><strong>Conclusions: </strong>This systematic review highlighted the potential of the abscopal effect in GBM, demonstrating its ability to enhance anti-tumor immune responses both locally and systemically. The synergistic effects of combinatorial approaches showed promise for improving outcomes. However, the low methodological quality of existing studies underscored the need for more rigorous preclinical research. Future studies should focus on improving research transparency, exploring the abscopal effect in other primary CNS neoplasms, and translating these findings into clinical trials to assess safety and efficacy in humans.</p>","PeriodicalId":16425,"journal":{"name":"Journal of Neuro-Oncology","volume":" ","pages":"77-87"},"PeriodicalIF":3.2000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Treatment-induced ripple effect: a systematic review exploring the abscopal phenomenon in Glioblastoma multiforme.\",\"authors\":\"Ali Haider Bangash, Prabhat Poudel, Khalid M Alshuqayfi, Mudassir Ahmed, Oluwaseun O Akinduro, Walid Ibn Essayed, Afshin Salehi, Rafael De la Garza Ramos, Reza Yassari, Harminder Singh, Jason P Sheehan, Yoshua Esquenazi\",\"doi\":\"10.1007/s11060-024-04912-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>This systematic review aimed to collate and synthesize the available literature on the abscopal effect in Glioblastoma multiforme (GBM) neoplasms, focusing on the reported biochemical mechanisms driving the abscopal effect.</p><p><strong>Methods: </strong>A systematic search was conducted in PubMed, Cochrane Database of Systematic Reviews, and Epistemonikos from inception to May 1, 2023. 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引用次数: 0
摘要
目的:本系统综述旨在整理和综合有关多形性胶质母细胞瘤(GBM)肿瘤abscopal效应的现有文献,重点介绍abscopal效应的生化机制。方法:系统检索PubMed、Cochrane Database of systematic Reviews和Epistemonikos数据库,检索时间为建站至2023年5月1日。包括探讨GBM的体外效应的研究。动物临床前研究临床相关性评估(RAA)工具用于评估临床前研究的方法学质量。系统地提取和合成了临床前模型、生化机制和结果的数据。结果:在总共7项研究中,5项临床前研究符合纳入标准。研究使用了多种体内小鼠模型,包括双侧肿瘤模型和免疫人源化小鼠。确定的关键生化机制包括免疫原性细胞死亡、危险相关分子模式释放、巨噬细胞激活和T细胞反应增强。包括溶瘤病毒治疗、纳米颗粒治疗、放射治疗和免疫检查点抑制剂在内的组合方法在诱导体外效应方面显示出希望。据报道,治疗动物的肿瘤生长受到明显抑制,生存得到改善。然而,RAA分析强调了对研究透明度和研究内部有效性的关注。结论:本系统综述强调了体外作用在GBM中的潜力,证明了其增强局部和全身抗肿瘤免疫反应的能力。组合方法的协同效应显示出改善结果的希望。然而,现有研究的低方法学质量强调了更严格的临床前研究的必要性。未来的研究应侧重于提高研究透明度,探索其他原发性中枢神经系统肿瘤的体外效应,并将这些发现转化为临床试验,以评估人类的安全性和有效性。
Treatment-induced ripple effect: a systematic review exploring the abscopal phenomenon in Glioblastoma multiforme.
Purpose: This systematic review aimed to collate and synthesize the available literature on the abscopal effect in Glioblastoma multiforme (GBM) neoplasms, focusing on the reported biochemical mechanisms driving the abscopal effect.
Methods: A systematic search was conducted in PubMed, Cochrane Database of Systematic Reviews, and Epistemonikos from inception to May 1, 2023. Studies exploring the abscopal effect in GBM were included. The Clinical Relevance Assessment of Animal Preclinical research (RAA) tool was used to assess methodological quality of preclinical studies. Data on preclinical models, biochemical mechanisms, and outcomes were extracted and synthesized systrmatically.
Results: Out of a total of 7 studies, five preclinical studies met the inclusion criteria. The studies utilized various in vivo mouse models, including bilateral tumor models and immunohumanized mice. Key biochemical mechanisms identified included immunogenic cell death, danger-associated molecular pattern release, macrophage activation, and enhanced T cell responses. Combinatorial approaches involving oncolytic virotherapy, nanoparticle-based treatments, radiation therapy, and immune checkpoint inhibitors showed promise in inducing abscopal effects. Significant tumor growth inhibition and improved survival were reported in treated animals. However, the RAA analysis highlighted concerns regarding research transparency and internal validity across studies.
Conclusions: This systematic review highlighted the potential of the abscopal effect in GBM, demonstrating its ability to enhance anti-tumor immune responses both locally and systemically. The synergistic effects of combinatorial approaches showed promise for improving outcomes. However, the low methodological quality of existing studies underscored the need for more rigorous preclinical research. Future studies should focus on improving research transparency, exploring the abscopal effect in other primary CNS neoplasms, and translating these findings into clinical trials to assess safety and efficacy in humans.
期刊介绍:
The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.