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. 2014 Apr 1;20(7):1884-90.
doi: 10.1158/1078-0432.CCR-13-2649. Epub 2014 Jan 29.

Circulating oncometabolite 2-hydroxyglutarate is a potential surrogate biomarker in patients with isocitrate dehydrogenase-mutant intrahepatic cholangiocarcinoma

Affiliations

Circulating oncometabolite 2-hydroxyglutarate is a potential surrogate biomarker in patients with isocitrate dehydrogenase-mutant intrahepatic cholangiocarcinoma

Darrell R Borger et al. Clin Cancer Res. .

Abstract

Purpose: 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.

Experimental design: 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.

Results: 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.

Conclusions: 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.

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Figures

Figure 1
Figure 1
The distribution of circulating 2HG levels in blood samples collected across the two cohorts. Serum 2HG levels were measured and compared between patients with IDH1-mutant or IDH2-mutant (IDH-Mut) versus IDH-wild-type (IDH-WT) ICCs in the A) Screening cohort (n=31) and B) in the Validation cohort (n=38). For each column, the dark grey box represents the 2HG values in the 75th quartile and the light grey box represents values in the 50th quartile. The lines extending vertically from the boxes indicate the variability outside the upper and lower quartiles. A significant elevation of circulating 2HG levels was seen in IDH-Mut ICC patients compared to IDH-WT ICC patients (p<0.001).
Figure 2
Figure 2
Correlation between serum 2HG level and tumor volume measured at surgery in IDH1-mutant and IDH2-mutant ICC patients from the Validation cohort.

References

    1. Shaib YH, Davila JA, McGlynn K, El-Serag HB. Rising incidence of intrahepatic cholangiocarcinoma in the United States: a true increase? Journal of hepatology. 2004;40(3):472–7. Epub 2004/05/05. - PubMed
    1. Poultsides GA, Zhu AX, Choti MA, Pawlik TM. Intrahepatic cholangiocarcinoma. The Surgical clinics of North America. 2010;90(4):817–37. Epub 2010/07/20. - PubMed
    1. Valle J, Wasan H, Palmer DH, Cunningham D, Anthoney A, Maraveyas A, et al. Cisplatin plus gemcitabine versus gemcitabine for biliary tract cancer. The New England journal of medicine. 2010;362(14):1273–81. Epub 2010/04/09. - PubMed
    1. Hezel AF, Deshpande V, Zhu AX. Genetics of biliary tract cancers and emerging targeted therapies. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2010;28(21):3531–40. Epub 2010/06/16. - PMC - PubMed
    1. Sia D, Tovar V, Moeini A, Llovet JM. Intrahepatic cholangiocarcinoma: pathogenesis and rationale for molecular therapies. Oncogene. 2013 Epub 2013/01/16. - PMC - PubMed

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