Aldaz Paula, Arozarena Imanol
Cancer Signaling Unit, Navarrabiomed, Hospital Universitario de Navarra (HUN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Health Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.
Cancers (Basel). 2021 Nov 18;13(22):5799. doi: 10.3390/cancers13225799.
Glioblastoma (GBM) is the most common and lethal form of malignant brain tumor. GBM patients normally undergo surgery plus adjuvant radiotherapy followed by chemotherapy. Numerous studies into the molecular events driving GBM highlight the central role played by the Epidermal Growth Factor Receptor (EGFR), as well as the Platelet-derived Growth Factor Receptors PDGFRA and PDGFRB in tumor initiation and progression. Despite strong preclinical evidence for the therapeutic potential of tyrosine kinase inhibitors (TKIs) that target EGFR, PDGFRs, and other tyrosine kinases, clinical trials performed during the last 20 years have not led to the desired therapeutic breakthrough for GBM patients. While clinical trials are still ongoing, in the medical community there is the perception of TKIs as a lost opportunity in the fight against GBM. In this article, we review the scientific rationale for the use of TKIs targeting glioma drivers. We critically analyze the potential causes for the failure of TKIs in the treatment of GBM, and we propose alternative approaches to the clinical evaluation of TKIs in GBM patients.
胶质母细胞瘤(GBM)是最常见且致命的恶性脑肿瘤形式。GBM患者通常先接受手术,再进行辅助放疗,随后进行化疗。众多关于驱动GBM的分子事件的研究突出了表皮生长因子受体(EGFR)以及血小板衍生生长因子受体PDGFRA和PDGFRB在肿瘤起始和进展中所起的核心作用。尽管针对EGFR、PDGFRs和其他酪氨酸激酶的酪氨酸激酶抑制剂(TKIs)的治疗潜力有强有力的临床前证据,但过去20年进行的临床试验并未为GBM患者带来预期的治疗突破。虽然临床试验仍在进行中,但在医学界,TKIs被视为在对抗GBM斗争中错失的机会。在本文中,我们回顾了使用靶向胶质瘤驱动因子的TKIs的科学依据。我们批判性地分析了TKIs治疗GBM失败的潜在原因,并提出了对GBM患者进行TKIs临床评估的替代方法。