Borger Darrell R, Goyal Lipika, Yau Thomas, Poon Ronnie T, Ancukiewicz Marek, Deshpande Vikram, Christiani David C, Liebman Hannah M, Yang Hua, Kim Hyeryun, Yen Katharine, Faris Jason E, Iafrate A John, Kwak Eunice L, Clark Jeffrey W, Allen Jill N, Blaszkowsky Lawrence S, Murphy Janet E, Saha Supriya K, Hong Theodore S, Wo Jennifer Y, Ferrone Cristina R, Tanabe Kenneth K, Bardeesy Nabeel, Straley Kimberly S, Agresta Sam, Schenkein David P, Ellisen Leif W, Ryan David P, Zhu Andrew X
Authors' Affiliations: Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston; Agios Pharmaceuticals, Cambridge, Massachusetts; and Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Clin Cancer Res. 2014 Apr 1;20(7):1884-90. doi: 10.1158/1078-0432.CCR-13-2649. Epub 2014 Jan 29.
Mutations in the IDH1 and IDH2 (IDH1/2) genes occur in approximately 20% of intrahepatic cholangiocarcinoma and lead to accumulation of 2-hydroxyglutarate (2HG) in the tumor tissue. However, it remains unknown whether IDH1/2 mutations can lead to high levels of 2HG circulating in the blood and whether serum 2HG can be used as a biomarker for IDH1/2 mutational status and tumor burden in intrahepatic cholangiocarcinoma.
We initially measured serum 2HG concentration in blood samples collected from 31 patients with intrahepatic cholangiocarcinoma in a screening cohort. Findings were validated across 38 resected patients with intrahepatic cholangiocarcinoma from a second cohort with tumor volume measures. Circulating levels of 2HG were evaluated relative to IDH1/2 mutational status, tumor burden, and a number of clinical variables.
Circulating levels of 2HG in the screening cohort were significantly elevated in patients with IDH1/2-mutant (median, 478 ng/mL) versus IDH1/2-wild-type (median, 118 ng/mL) tumors (P < 0.001). This significance was maintained in the validation cohort (343 ng/mL vs. 55 ng/mL, P < 0.0001) and levels of 2HG directly correlated with tumor burden in IDH1/2-mutant cases (P < 0.05). Serum 2HG levels ≥170 ng/mL could predict the presence of an IDH1/2 mutation with a sensitivity of 83% and a specificity of 90%. No differences were noted between the allelic variants IDH1 or IDH2 in regard to the levels of circulating 2HG.
This study indicates that circulating 2HG may be a surrogate biomarker of IDH1 or IDH2 mutation status in intrahepatic cholangiocarcinoma and that circulating 2HG levels may correlate directly with tumor burden. Clin Cancer Res; 20(7); 1884-90. ©2014 AACR.
异柠檬酸脱氢酶1和2(IDH1/2)基因的突变发生在约20%的肝内胆管癌中,并导致肿瘤组织中2-羟基戊二酸(2HG)的积累。然而,IDH1/2突变是否会导致血液中2HG水平升高以及血清2HG是否可作为肝内胆管癌IDH1/2突变状态和肿瘤负荷的生物标志物仍不清楚。
我们最初在一个筛查队列中测量了从31例肝内胆管癌患者采集的血样中的血清2HG浓度。在第二个队列中对38例接受手术切除的肝内胆管癌患者进行了验证,并测量了肿瘤体积。评估了2HG的循环水平与IDH1/2突变状态、肿瘤负荷及一些临床变量之间的关系。
在筛查队列中,IDH1/2突变型肿瘤(中位数,478 ng/mL)患者的2HG循环水平显著高于IDH1/2野生型肿瘤(中位数,118 ng/mL)患者(P < 0.001)。在验证队列中这一显著性得以维持(343 ng/mL对55 ng/mL,P < 0.0001),并且在IDH1/2突变病例中2HG水平与肿瘤负荷直接相关(P < 0.05)。血清2HG水平≥170 ng/mL可预测IDH1/2突变的存在,敏感性为83%,特异性为90%。在循环2HG水平方面,未观察到IDH1或IDH2等位基因变体之间存在差异。
本研究表明,循环2HG可能是肝内胆管癌中IDH1或IDH2突变状态的替代生物标志物,并且循环2HG水平可能与肿瘤负荷直接相关。《临床癌症研究》;20(7);1884 - 1890。©2014美国癌症研究协会。