Qin Chaoying, Long Wenyong, Zhang Chi, Xie Yuanyang, Wu Changwu, Li Yang, Xiao Qun, Ji Nan, Liu Qing
Department of Neurosurgery in Xiangya Hospital, Central South University, Changsha, China.
Department of Neurosurgery in Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Front Oncol. 2020 Sep 29;10:522816. doi: 10.3389/fonc.2020.522816. eCollection 2020.
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. We present a pregnant female at 20 weeks gestation diagnosed with GBM. Surgical resection was initially performed without adjuvant therapy, and the tumor recurred 2 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. 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.
胶质母细胞瘤(GBM)是成人中最恶性的颅内肿瘤。然而,关于妊娠期GBM的整体治疗鲜有报道。如何平衡对母亲的治疗益处和对胎儿的风险,对临床医生来说仍然极具挑战性。特异性靶向治疗与传统治疗相结合的应用为患有GBM的患者带来了更长的生存期。我们报告了一名妊娠20周时被诊断为GBM的女性。最初进行了手术切除,未进行辅助治疗,2个月后肿瘤复发。在妊娠32周时同时进行了二次开颅手术和剖宫产,患者和婴儿均存活。随后她接受了传统的放化疗。除了BRAF V600E突变外,未检测到其他表明预后乐观的基因改变。因此,给她使用了BRAF抑制剂,取得了超过2年无复发存活的良好临床效果。当妊娠期发生GBM时,应考虑个性化的多学科治疗。本病例对治疗的反应表明,BRAF V600E突变是GBM的一个有利生物标志物。通过基因检测和靶向治疗可能降低GBM的死亡率。然而,必须进行更多研究来证实我们的观察结果。