Osimertinib in Combination with Bevacizumab for EGFR Mutated Recurrent Glioblastoma (GBM): A Case Report

Soma Sengupta
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Abstract

Glioblastoma is the most common primary, malignant adult brain tumor with a median overall survival of 12-15 months after diagnosis. The standard of care includes maximal safe resection, chemoradiation, adjuvant chemotherapy with the DNA alkylator, temozolomide and tumor-treating fields. Given the recent advances in targeted molecular therapeutics and tissue sequencing, there is a growing opportunity for precision medicine in GBM treatment. In this case report, we present two patients who were found to have EGFR amplifications on molecular analysis and were treated with the EGFR inhibitor, osimertinib (Tagrisso), in combination with bevacizumab (Avastin) after tumor progression. One patient received osimertinib at first GBM progression, while the other patient received osimertinib after two other treatment regimens had failed. Both patients displayed radiographic stability several months after the expected median overall survival rate of 15 months post-diagnosis for GBM. This case report offers clinical vignettes in support of the use of EGFR inhibitors and bevacizumab in recurrent GBM with EGFR mutations.
奥希替尼联合贝伐单抗治疗表皮生长因子受体(EGFR)突变的复发性胶质母细胞瘤(GBM):病例报告
胶质母细胞瘤是最常见的原发性成人恶性脑肿瘤,确诊后的中位总生存期为 12-15 个月。标准治疗包括最大限度安全切除、化学放疗、DNA 烷化剂替莫唑胺辅助化疗和肿瘤治疗领域。鉴于分子靶向治疗和组织测序的最新进展,GBM 治疗中的精准医疗机会越来越多。在本病例报告中,我们介绍了两名在分子分析中发现表皮生长因子受体扩增的患者,他们在肿瘤进展后接受了表皮生长因子受体抑制剂奥西替尼(Tagrisso)联合贝伐珠单抗(Avastin)的治疗。其中一名患者在 GBM 首次进展时接受了奥希替尼治疗,另一名患者则在其他两种治疗方案失败后接受了奥希替尼治疗。这两名患者都在 GBM 诊断后 15 个月的预期中位总生存率之后数月才显示出放射学上的稳定性。本病例报告提供了一些临床案例,支持将表皮生长因子受体抑制剂和贝伐单抗用于表皮生长因子受体突变的复发性 GBM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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