Sherman Wendy Joyce, Vitaz Todd W
Department of Neurology and Neurosurgery, Mayo Clinic, Jacksonville, FL, USA
Department of Neurosurgery, Spectrum Health, Grand Rapids, MI, USA.
BMJ Case Rep. 2021 Apr 27;14(4):e241026. doi: 10.1136/bcr-2020-241026.
Lynch syndrome is an autosomal dominant disorder leading to cancer predisposition caused by mutations in mismatch repair genes. There is minimal published experience treating glioblastoma in patients with Lynch syndrome. We report a patient with Lynch syndrome who was initially diagnosed with a left occipital isocitrate dehydrogenase (IDH) wild-type glioblastoma. After resection, she was treated with chemoradiation, followed by tumour treating fields. Three years after diagnosis, recurrence was resected. After refusing cytotoxic chemotherapy, decision was made to treat with off-label nivolumab concurrently with radiation. She has been maintained on nivolumab without recurrence of her glioblastoma now over 5 years out from her initial diagnosis. This case provides the first report of glioblastoma in a patient with Lynch syndrome responding to nivolumab and concurrent radiation. In patients with Lynch syndrome and glioblastoma, immunotherapy in the form of nivolumab may be an alternative option to standard cytotoxic chemotherapy.
林奇综合征是一种常染色体显性疾病,由错配修复基因的突变导致癌症易感性。关于治疗林奇综合征患者的胶质母细胞瘤,公开的经验很少。我们报告了一名林奇综合征患者,最初被诊断为左枕叶异柠檬酸脱氢酶(IDH)野生型胶质母细胞瘤。切除术后,她接受了放化疗,随后接受了肿瘤电场治疗。诊断三年后,复发肿瘤被切除。在拒绝细胞毒性化疗后,决定使用未获批准的纳武单抗联合放疗进行治疗。自最初诊断以来,她已接受纳武单抗维持治疗超过5年,胶质母细胞瘤未复发。本病例首次报告了林奇综合征患者的胶质母细胞瘤对纳武单抗和同步放疗有反应。对于林奇综合征和胶质母细胞瘤患者,纳武单抗形式的免疫疗法可能是标准细胞毒性化疗的替代选择。