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免疫检查点抑制作为 CMMRD 患者伴 -突变间变性星形细胞瘤的主要辅助治疗:案例报告——免疫检查点抑制在 CMMRD 中的应用。

Immune Checkpoint Inhibition as Primary Adjuvant Therapy for an -Mutant Anaplastic Astrocytoma in a Patient with CMMRD: A Case Report-Usage of Immune Checkpoint Inhibition in CMMRD.

机构信息

Section of Hematology/Oncology, Department of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3E 0V9, Canada.

Department of Biochemistry and Medical Genetics, Max Rady College of Medicine, University of Manitoba, Winnipeg, MB R3E 0J9, Canada.

出版信息

Curr Oncol. 2021 Feb 1;28(1):757-766. doi: 10.3390/curroncol28010074.

Abstract

Constitutional mismatch repair deficiency (CMMRD) is a rare autosomal recessive hereditary cancer syndrome due to biallelic germline mutation involving one of the four DNA mismatch repair genes. Here we present a case of a young female with CMMRD, homozygous for the c.2002A>G mutation in the gene. She developed an early stage adenocarcinoma of the colon at the age of 14. Surveillance MRI of the brain at age 18 resulted in the detection of an asymptomatic brain cancer. On resection, this was diagnosed as an anaplastic astrocytoma. Due to emerging literature suggesting benefit of immunotherapy in this patient population, she was treated with adjuvant dual immune checkpoint inhibition, avoiding radiation. The patient remains stable with no evidence of progression 20 months after resection. The patient's clinical course, as well as the rational for considering adjuvant immunotherapy in patients with CMMRD are discussed in this report.

摘要

错配修复缺陷(CMMRD)是一种罕见的常染色体隐性遗传性癌症综合征,由于涉及四个 DNA 错配修复基因之一的双等位基因种系突变引起。本文报道了一例 CMMRD 年轻女性患者,其 基因的 c.2002A>G 突变纯合子。她在 14 岁时患有早期结肠癌。18 岁时进行脑的 MRI 监测,发现无症状性脑癌。切除后,诊断为间变性星形细胞瘤。由于新出现的文献表明免疫疗法对这类患者人群有益,她接受了辅助性双重免疫检查点抑制治疗,避免了放疗。患者在切除后 20 个月,病情稳定,没有进展迹象。本文讨论了患者的临床过程以及在 CMMRD 患者中考虑辅助免疫治疗的理由。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aa1/7985791/f688e3f8ebeb/curroncol-28-00074-g001a.jpg

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