Multidisciplinary Therapy Managed Recurrent Glioblastoma in a BRAF-V600E Mutant Pregnant Female: A Case Report and Review of the Literature

被引:6
作者
Qin, Chaoying [1 ]
Long, Wenyong [1 ]
Zhang, Chi [1 ]
Xie, Yuanyang [1 ]
Wu, Changwu [1 ]
Li, Yang [1 ]
Xiao, Qun [1 ]
Ji, Nan [2 ]
Liu, Qing [1 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Neurosurg, Changsha, Peoples R China
[2] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurosurg, Beijing, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
基金
中国国家自然科学基金;
关键词
glioblastoma (GBM); pregnancy; multidisciplinary therapy (MDT); BRAF V600E; vemurafenib; CENTRAL-NERVOUS-SYSTEM; BRAF V600E MUTATION; MULTIFORME; TUMORS; CLASSIFICATION; RADIOTHERAPY; TEMOZOLOMIDE; MULTICENTER; MELANOMA; GLIOMA;
D O I
10.3389/fonc.2020.522816
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background:Glioblastoma (GBM) is the most malignant intracranial tumor in adults. However, the overall management of GBM in pregnancy is rarely reported. How to balance the therapeutic benefits to the mother and risks to the fetus remains hugely challenging for clinicians. The application of specific targeting therapy combined with conventional treatment sheds light on a longer lifetime for the patients suffering from GBM. Case Presentation:We present a pregnant female at 20 weeks gestation diagnosed with GBM. Surgical resection was initially performed without adjuvant therapy, and the tumor recurredde novo2 months later. A secondary craniotomy and cesarean section were performed simultaneously at 32 weeks gestation, both the patient and infant were survived. She was subsequently treated with traditional chemo-radiotherapy. No other identified genetic alterations indicating an optimistic prognosis were detected except for BRAF V600E mutation. Thus, the BRAF inhibitor was placed on her with achieving a good clinical outcome of more than 2-year survival without recurrence. Conclusion:Personalized multidisciplinary therapy should be considered when GBMs occur in pregnancy. Response to the therapy in this presenting case suggests that BRAF V600E mutation is a favorable biomarker for GBM. The mortality of GBM might be reduced through genetic testing and targeted treatment. However, more studies must be conducted to confirm our observation.
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页数:9
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