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肿瘤基因组分析指导转移性胃癌患者接受靶向治疗:VIKTORY 伞式试验。

Tumor Genomic Profiling Guides Patients with Metastatic Gastric Cancer to Targeted Treatment: The VIKTORY Umbrella Trial.

机构信息

Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Division of Gastroenterology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Cancer Discov. 2019 Oct;9(10):1388-1405. doi: 10.1158/2159-8290.CD-19-0442. Epub 2019 Jul 17.

Abstract

The VIKTORY (targeted agent eValuation In gastric cancer basket KORea) trial was designed to classify patients with metastatic gastric cancer based on clinical sequencing and focused on eight different biomarker groups ( aberration, mutation, mutation/amplification, amplification, MET overexpression, all negative, deficient, or amplification) to assign patients to one of the 10 associated clinical trials in second-line (2L) treatment. Capivasertib (AKT inhibitor), savolitinib (MET inhibitor), selumetinib (MEK inhibitor), adavosertib (WEE1 inhibitor), and vistusertib (TORC inhibitor) were tested with or without chemotherapy. Seven hundred seventy-two patients with gastric cancer were enrolled, and sequencing was successfully achieved in 715 patients (92.6%). When molecular screening was linked to seamless immediate access to parallel matched trials, 14.7% of patients received biomarker-assigned drug treatment. The biomarker-assigned treatment cohort had encouraging response rates and survival when compared with conventional 2L chemotherapy. Circulating tumor (ctDNA) analysis demonstrated good correlation between high copy number by ctDNA and response to savolitinib. SIGNIFICANCE: Prospective clinical sequencing revealed that baseline heterogeneity between tumor samples from different patients affected response to biomarker-selected therapies. VIKTORY is the first and largest platform study in gastric cancer and supports both the feasibility of tumor profiling and its clinical utility..

摘要

VIKTORY(胃癌篮子韩国靶向药物评估)试验旨在根据临床测序对转移性胃癌患者进行分类,并侧重于八个不同的生物标志物组(异常、突变、突变/扩增、扩增、MET 过表达、全部阴性、缺陷或扩增),将患者分配到二线(2L)治疗的 10 个相关临床试验之一。卡匹维泮(AKT 抑制剂)、萨沃替尼(MET 抑制剂)、塞尔美替尼(MEK 抑制剂)、阿伐索替尼(WEE1 抑制剂)和维特索替尼(TORC 抑制剂)进行了有或没有化疗的测试。共招募了 772 例胃癌患者,715 例(92.6%)成功进行了测序。当分子筛选与无缝即时获得平行匹配试验相关联时,14.7%的患者接受了生物标志物分配药物治疗。与传统的 2L 化疗相比,生物标志物分配治疗组的反应率和生存率令人鼓舞。循环肿瘤(ctDNA)分析表明,ctDNA 高拷贝数与对萨沃替尼的反应之间存在良好的相关性。意义:前瞻性临床测序表明,来自不同患者的肿瘤样本之间的基线异质性影响了对生物标志物选择疗法的反应。VIKTORY 是胃癌的首个也是最大的平台研究,支持肿瘤分析的可行性及其临床实用性。

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