Arshad Junaid, Barreto-Coelho Priscila, Jonczak Emily, Espejo Andrea, D'Amato Gina, Trent Jonathan C
Department of Medicine, Division of Medical Oncology, Miller School of Medicine, Jackson Memorial Hospital/University of Miami, Miami, FL, USA.
Department of Medicine, Division of Internal Medicine, Miller School of Medicine, Jackson Memorial Hospital/University of Miami, Miami, FL, USA.
J Immunother Precis Oncol. 2020 Jun 5;3(2):64-68. doi: 10.36401/JIPO-20-3. eCollection 2020 May.
Leiomyosarcoma is a malignant mesenchymal tumor of cells of smooth muscle lineage arising commonly in retroperitoneum, uterus, large veins, and the limbs. The genetics of leiomyosarcomas are complex and there is very limited understanding of common driver mutations. Circulating tumor DNA (ctDNA) offers a rapid and noninvasive method of next-generation sequencing (NGS) that could be used for diagnosis, therapy, and detection of recurrence.
ctDNA testing was performed using Guardant360, which detects single nucleotide variants, amplifications, fusions, and specific insertion/deletion mutations in 73 genes using NGS.
Of 73 patients, 59 were found to have one or more cancer-associated genomic alteration. Forty-five (76%) were female with a median age of 63 (range, 38-87) years. All samples were designated metastatic. The most common alterations were detected in Tp53 (65%), BRAF (13%), CCNE (13%), EGFR (12%), PIK3CA (12%), FGFR1 (10%), RB1(10%), KIT (8%), and PDGFRA (8%). Some of the other alterations included RAF1, ERBB2, MET, PTEN TERT, APC, and NOTCH1. Potentially targetable mutations, by Food and Drug Administration-approved or clinical trials, were found in 24 (40%) of the 73 patients. Four patients (5%) were found to have incidental germline TP53 mutations.
NGS of ctDNA allows identification of genomic alterations in plasma from patients with leiomyosarcoma. Unfortunately, there is limited activity of current targeted agents in leiomyosarcomas. These results suggest opportunities to develop therapy against TP53, cell cycle, and kinase signaling pathways. Further validation and prospective evaluation is warranted to investigate the clinical utility of ctDNA for patients with leiomyosarcoma.
平滑肌肉瘤是一种起源于平滑肌谱系细胞的恶性间叶组织肿瘤,常见于腹膜后、子宫、大静脉和四肢。平滑肌肉瘤的遗传学很复杂,人们对常见的驱动突变了解非常有限。循环肿瘤DNA(ctDNA)提供了一种快速且无创的下一代测序(NGS)方法,可用于诊断、治疗和复发检测。
使用Guardant360进行ctDNA检测,该方法通过NGS检测73个基因中的单核苷酸变异、扩增、融合以及特定的插入/缺失突变。
在73例患者中,59例被发现有一个或多个与癌症相关的基因组改变。45例(76%)为女性,中位年龄为63岁(范围38 - 87岁)。所有样本均被认定为转移性。最常见的改变见于Tp53(65%)、BRAF(13%)、CCNE(13%)、EGFR(12%)、PIK3CA(12%)、FGFR1(10%)、RB1(10%)、KIT(8%)和PDGFRA(8%)。其他一些改变包括RAF1、ERBB2、MET、PTEN、TERT、APC和NOTCH1。在73例患者中的24例(40%)发现了可被美国食品药品监督管理局批准的或临床试验中的潜在可靶向突变。4例患者(5%)被发现有偶然的胚系TP53突变。
ctDNA的NGS能够识别平滑肌肉瘤患者血浆中的基因组改变。遗憾的是,目前的靶向药物在平滑肌肉瘤中的活性有限。这些结果提示了针对TP53、细胞周期和激酶信号通路开发治疗方法的机会。有必要进行进一步验证和前瞻性评估,以研究ctDNA对平滑肌肉瘤患者的临床应用价值。