- Research article
- Open Access
Genome-wide copy number alteration and VEGFA amplification of circulating cell-free DNA as a biomarker in advanced hepatocellular carcinoma patients treated with Sorafenib
BMC Cancer volume 19, Article number: 292 (2019)
Although sorafenib is the global standard first-line systemic treatment for unresectable hepatocellular carcinoma (HCC), it does not have reliable predictive or prognostic biomarkers. Circulating cell-free DNA (cfDNA) has shown promise as a biomarker for various cancers. We investigated the use of cfDNA to predict clinical outcomes in HCC patients treated with sorafenib.
This prospective biomarker study analyzed plasma cfDNA from 151 HCC patients who received first-line sorafenib and 14 healthy controls. The concentration and VEGFA-to-EIF2C1 ratios (the VEGFA ratio) of cfDNA were measured. Low depth whole-genome sequencing of cfDNA was used to identify genome-wide copy number alteration (CNA), and the I-score was developed to express genomic instability. The I-score was defined as the sum of absolute Z-scores of sequenced reads on each chromosome. The primary aim of this study was to develop cfDNA biomarkers predicting treatment outcomes of sorafenib, and the primary study outcome was the association between biomarkers with treatment efficacy including disease control rate (DCR), time to progression (TTP) and overall survival (OS) in these patients.
The cfDNA concentrations were significantly higher in HCC patients than in healthy controls (0.71 vs. 0.34 ng/μL; P < 0.0001). Patients who did not achieve disease control with sorafenib had significantly higher cfDNA levels (0.82 vs. 0.63 ng/μL; P = 0.006) and I-scores (3405 vs. 1024; P = 0.0017) than those achieving disease control. The cfDNA-high group had significantly worse TTP (2.2 vs. 4.1 months; HR = 1.71; P = 0.002) and OS (4.1 vs. 14.8 months; HR = 3.50; P < 0.0001) than the cfDNA-low group. The I-score-high group had poorer TTP (2.2 vs. 4.1 months; HR = 2.09; P < 0.0001) and OS (4.6 vs. 14.8 months; HR = 3.35; P < 0.0001). In the multivariable analyses, the cfDNA remained an independent prognostic factor for OS (P < 0.0001), and the I-score for both TTP (P = 0.011) and OS (P = 0.010). The VEGFA ratio was not significantly associated with treatment outcomes.
Pretreatment cfDNA concentration and genome-wide CNA in cfDNA are potential biomarkers predicting outcomes in advanced HCC patients receiving first-line sorafenib.
Primary liver cancer is a deadly malignancy, with 782,500 new cases and 745,500 deaths reported worldwide in 2012 . Liver cancer ranks 2nd and 6th highest as the cause of cancer-related death in men and women, respectively, and remains an important public health issue in the world . Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer and accounts for approximately 75–90% of all liver cancers. [1, 2] Advanced unresectable HCC is among the most difficult-to-treat cancers because of its resistance to systemic chemotherapy and underlying liver dysfunction. Systemic chemotherapy was not recommended until 2007, when the molecular targeted agent sorafenib, an inhibitor of vascular endothelial growth factor (VEGF) receptor, platelet-derived growth factor receptor, Raf family kinases, and other tyrosine kinases, demonstrated survival benefits in advanced HCC patients [3, 4]. Although sorafenib is the global standard first-line systemic treatment for advanced unresectable HCC, it does not have reliable predictive or prognostic biomarkers [3, 4]. Several studies suggested the potential biomarkers include soluble c-Kit and hepatocyte growth factor in plasma, and VEGFA amplification in tumor tissues as predictive markers [5, 6], or alpha-fetoprotein (AFP), alkaline phosphatase, angiopoietin 2, VEGF, and neutrophil-to-lymphocyte ratio in the blood as prognostic markers [5, 7]; however, these biomarkers have not been validated or translated into clinical practice. Recent data reported that VEGFA could promote tumor development and growth in a preclinical model of HCC and suggested VEGFA genomic amplification in HCC tumor tissues as a predictive biomarker for sorafenib based on results showing survival of patients with HCC who did not receive sorafenib was independent of VEGFA status in tumor tissue, whereas markedly improved survival was seen in the VEGFA-amplification group compared with the non- amplification group in sorafenib-treated patients [6, 8].
Circulating tumor DNA (ctDNA) has the potential to reveal tumor genetic and epigenetic information while overcoming obstacles related to tumor heterogeneity and clonal evolution; thus cfDNA holds great promise as a liquid biopsy. Given that HCC is frequently diagnosed using radiologic imaging without pathologic confirmation, and biopsy for this cancer is associated with a relatively high risk of bleeding risk for biopsy, ctDNA in the peripheral blood would be especially useful in HCC. Previous studies have reported that the presence of ctDNA reflected tumor progression after surgery in HCC, and high cfDNA concentration was associated with larger tumors, higher tumor grade, and shorter overall survival after surgery, and may serve as a predictive biomarker for distant metastasis after curative surgery in HCC [9, 10]. However, there are no data about the prognostic role of cfDNA concentrations in the setting of advanced HCC treated with systemic treatment.
To develop novel cfDNA-based biomarkers as predictors of outcome in HCC patients treated with sorafenib, we evaluated cfDNA concentration itself and genetic alterations in cfDNA focusing on 1) a specific gene, VEGFA amplification based on previous data suggesting VEGFA amplification in tumor tissue as a potential biomarker for sorafenib [6, 8], and 2) genome-wide copy number alterations (CNAs).
The primary aim of this study was to develop cfDNA biomarkers predicting disease control rate (DCR), time to progression (TTP), and overall survival (OS) in patients who had advanced or metastatic HCC not amenable to local therapies and were treated with first-line sorafenib.
Study design and population
This prospective biomarker study was performed in the subpopulation who received first-line sorafenib among the entire study population in an open-label, exploratory, observational, biomarker study in patients who had advanced or metastatic HCC not amenable to local therapies and were treated with systemic therapy. Longitudinal blood samples ± tissue samples including baseline samples before treatment were prospectively collected in eligible patients.
This study was conducted under approval from the Institutional Review Board at Asan Medical Center, Korea (IRB No. 2014–1208). Patients were included in this study if they met the following criteria: 1) age ≥ 18 years; 2) histologically or radiologically confirmed advanced or metastatic HCC not amenable to local therapies; 3) first-line treatment with sorafenib; 4) measurable or evaluable lesion(s) according to the Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1 ; and 5) available peripheral blood samples obtained before the start of sorafenib for cfDNA analysis. Exclusion criteria were as follows: 1) fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC; 2) prior systemic treatment for HCC; 3) concurrent other malignancy; and 4) no available imaging study for evaluation of response to sorafenib. All patients provided written informed consent before study enrollment. Clinical data of patients were prospectively collected.
Plasma samples from 14 healthy volunteers were used as negative controls and were collected after obtaining signed informed consent from each patient.
Treatment and assessment
Patients received sorafenib 400 mg twice a day, and dose reduction was allowed at the discretion of the physician. Treatment was continued until progressive disease (PD), patient withdrawal, or unacceptable toxicity.
Tumor response was evaluated using computed tomography according to RECIST version 1.1 every 6–8 weeks. DCR was defined as the percentage of patients with best tumor response of complete response (CR), partial response, or stable disease (or non-CR/non-PD in the case of non-measurable disease). OS was defined as the time from initiation of sorafenib to death from any cause, and TTP was defined as the time until radiologic disease progression, respectively.
Blood sample collection and cfDNA extraction
Peripheral blood samples from patients before starting sorafenib or healthy donors were collected in EDTA tubes and centrifuged within 4 h at room temperature at 1600×g for 10 min first, and then 3000×g for 10 min to isolate the plasma, which was then stored at − 80 °C until cfDNA extraction. Plasma cfDNA was extracted from 1.5 mL of plasma from each patient with the QIAamp Circulating Nucleic Acid kit (Qiagen, Hilden, Germany) following the manufacturer’s instructions. The final DNA eluent (50 μL) was quantified by Qubit 2.0 Fluorometer with the qubit dsDNA HS (High Sensitivity) assay kit (Life Technology, Carlsbad, CA, USA).
Detection of VEGFA amplification
EIF2C1 was used as a reference to assess the copy number of the VEGFA gene because it is known to be expressed at ubiquitously at low to medium levels. Plasma VEGFA-to-EIF2C1 ratios (the VEGFA ratio) were determined using droplet digital polymerase chain reaction (ddPCR) on a QX200 Droplet Digital PCR System (Bio-Rad Laboratories). Fluorescent probes (FAM and HEX) were prepared from PrimePCR™ ddPCR™Copy Number Assay for ddPCR (dHsaCP2500483 for VEGFA and dHsaCP2500349 for EIF2C1) (Bio-Rad Laboratories, Pleasanton, CA, USA).
Each sample was partitioned into 20,000 droplets, and target and control (background) DNA were randomly, but uniformly, distributed among the droplets. Reactions were performed in 20 μL reaction volumes that consisted of extracted cfDNA (8 μL), 2× ddPCR supermix for the probe (10 μL), and 20× VEGFA and EIF2C1 probe (FAM/HEX) (1 μL). The reaction samples and generator oil are placed into a QX200 droplet generator, which uses specially developed reagents and microfluidics to partition each sample into 20,000 nanoliter-sized droplets. The generated droplets are transferred to a 96-well plate for PCR in a thermal cycler. Emulsified PCR reactions in a 96-well plate were run on an Eppendorf Mastercycler nexus gradient Thermal Cycler (Master Cycler, Eppendorf, Germany) at 95 °C for 10 min, followed by 40 cycles of 94 °C for 30 s, 55 °C for 60 s, and a 10 min incubation at 98 °C. The plates were read on a Bio-Rad QX200 droplet reader (Bio-Rad, Hercules, CA, USA) using the QuantaSoft v1.4.0 software (Bio-Rad) to assess the number of droplets positive for VEGFA and EIF2C1.
Library preparation for whole-genome sequencing
The DNA libraries were prepared using the TruSeq nano kit (Illumina Inc., San Diego, CA, USA). Briefly, approximately 5 ng of cfDNA was subjected to end repair, adenylation, and adaptor ligation. High sensitivity D1000 Screen Tape (Agilent Technologies, Santa Clara, CA, USA) was used to examine the size distribution of the final libraries. The pooled libraries of 24 samples per run were analyzed with the NextSeq 500 (Illumina Inc.) in a 75-base single-read mode.
Data analysis for calculation of genome instability
All generated reads were aligned to the human reference genome (hg19) using the BWA-mem algorithm (0.7.5.a) with default parameters . Then, Picard (v.1.9.6) tools (https://broadinstitute.github.io/picard/) were used to remove PCR duplicates. The reads, which were below the mapping quality of 60, were not used for further analysis. The autosomal genome was divided into 1 Mb bins. Of 2897 bins, 163 were not used because these bins were located in low mapping regions such as the centromere and telomere. GC bias correction using the LOESS algorithm was performed for 2734 bins . The GC-corrected read counts for each bin were determined, and the percentage of sequencing reads mapped to each bin was calculated and compared with the mean value of the 14 healthy control subjects for the respective bin. A Z-score statistic was calculated using each bin’s mean and standard deviation (SD). Zj values represent the Z-score of the specific bin, which can be expressed using the following formula:
To express whole genomic instability (chromosomal instability), we developed the I-score, which is the sum of the absolute Z-scores of all usable bins with Z-score > 2 or < − 2. The I-score is defined as follows:
As a surrogate marker of whole genome instability, higher I-score means higher chromosomal instability. I-score is expected to be zero in the normal persons without any cancer.
The primary study outcome was the association between biomarkers and treatment efficacy including DCR, TTP, and OS. The Mann-Whitney test and the chi-square test were used for continuous variable data and categorical data, respectively. Kaplan-Meier method and log-rank test were used to estimate and compare TTP and OS of patients according to the level of cfDNA biomarkers (high vs. low cfDNA concentration; high vs. low I-score; high vs. low VEGFA amplification). We dichotomized the level of cfDNA biomarkers into high- and low-groups based on the median value of each biomarker. In the case of I-score, patients were also divided into four quartiles based on I-score values. Patients who did not have events (disease progression for TTP and death for OS) were censored at their last tumor assessment for TTP and at the last follow-up for OS. Univariable analyses were performed to analyze the associations of cfDNA biomarkers and clinicopathological parameters with TTP and OS, and multivariable Cox regression was performed to evaluate the effect of cfDNA biomarkers on TTP and OS, after adjusting for clinicopathological parameters that were statistically significant in the univariable analysis. Hazard ratio (HR) and 95% confidence intervals (CIs) for variables included in the multivariable model were reported. All P values reported were two-sided, and P values < 0.05 were considered statistically significant.
Among 242 patients who were enrolled in the advanced or metastatic HCC biomarker study between March 2014 and November 2016, 91 patients were excluded due to not receiving sorafenib as first-line therapy (n = 20), absence of available baseline blood samples before sorafenib (n = 38), absence of follow-up imaging data after sorafenib (n = 13), absence of evaluable lesion(s) (n = 11), and mixed cholangiocarcinoma and HCC (n = 9), leaving 151 patients eligible for this analysis (Fig. 1). Baseline characteristics are described in Table 1. Most patients had hepatitis B virus infection-associated HCC with Barcelona Clinic Liver Cancer stage C, Child-Pugh Class A liver function, and Eastern Cooperative Oncology Group performance status 0–1.
Total concentration, VEGFA amplification, and genome-wide CNAs in plasma cfDNA
The median cfDNA concentration was 0.71 ng/μL (range, 0.13–15.00) in HCC patients (n = 151) and 0.34 ng/μL (range, 0.28–0.54) in healthy controls (n = 14) (P < 0.0001) (Fig. 2 a). The cfDNA concentrations were significantly higher in HCC patients than in healthy controls (P < 0.0001). Elevated cfDNA concentration was observed in 122 patients (80.8%; 95% CI, 74.5–87.1%) compared with the 90th percentile of healthy controls.
In a calibration experiment using cancer cell lines with VEGFA amplification (OE19), VEGFA amplification was robustly detected with a copy number of 9 to 10 (median, 9.7; range, 9.3–10.4). Although the VEGFA copy number was measured only in part of the HCC cohort (n = 41) and in healthy controls, it was significantly higher in HCC patients than in healthy controls (median, 2.50 [range, 2.06–3.50] vs. 2.17 [range, 2.02–2.44], respectively; P < 0.0001) (Fig. 2b).
Whole-genome sequencing was successful in all 151 HCC patients, with a median I-score of 1637 (range, 256–28,520). A Circos plot from 151 HCC patients in which the number of regions significantly deviated from euploidy is illustrated in Fig. 3a. Most frequent chromosomal arm alterations included copy number losses in 1p, 4q, and 8p, and gains of 1q and 8q. GISTIC analysis  identified significantly recurrent focal amplifications at 1q21.3(harboring MCL1), 7q31.2 (harboring MET), 8q24.21 (harboring MYC), 11q13.3(harboring CCND1 and FGF19), 13q34, 19p13.11, and deletions at 4q35.2, 8p21.2, 13q14.2(harboring RB1), 14q24.2, 17p13.1(harboring TP53) and 19p13.3 regions. Oncogenes and tumor suppressor genes are included in such recurrent regions which were previously known as significantly altered regions in HCC .
Deletion of chromosome 1p, 4q and 8p and gain of chromosome 1q and 8q were frequently observed. Although the I-score significantly correlated with the cfDNA concentration (P < 0.0001), the degree of correlation was not high (R2 = 0.24) (Additional file 1: Figure. S1). CNA profiles were expressed as linear genomic plots for three representative patients in Fig. 3b and d.
Association between VEGFA copy numbers and treatment outcomes
Although there was no patient who had CR, two patients (1.3%) achieved PR, and 94 patients (62.3%) had SD or non-CR/non-PD as best response to sorafenib, resulting in 63.6% of the DCR. DCR did not significantly differ between the VEGFA-high group (above the cohort median; 52.6% [95% CI, 30.1–75.1%]) and the VEGFA-low group (68.2% [95% CI, 48.7–87.7%]) (P = 0.309). Similarly, TTP did not differ between the VEGFA-high group (3.8 months; 95% CI, 1.5–6.0) and the VEGFA-low group (3.5 months; 95% CI, 2.5–4.5) (P = 0.781) (Additional file 1: Figure. S2a). Although the median OS was shorter in the VEGFA-high group (7.5 months; 95% CI, 3.2–11.8) than in the VEGFA-low group (12.8 months, 95% CI, 7.7–18.0), the difference was not statistically significant (P = 0.180) (Additional file 1: Figure. S2b). We defined VEGFA amplification as a higher value than “mean + 3 x standard deviation” of VEGFA copy number in healthy controls, and cut-off value was 2.60. When we analyzed treatment outcomes according to the VEGFA amplification, TTP and OS did not significantly differ between the amplification group (n = 16) and the non-amplification group (n = 25); the median TTP values were 3.8 months (95% CI, 1.1–6.5) and 3.5 months (95% CI, 2.1–4.9) (P = 0.725), respectively, and the median OS was 8.4 months (95% CI, 6.4–10.3) and 12.6 months (95% CI, 7.1–18.0), respectively (P = 0.626). The DCR was also not different between the two groups; 56.3% in the amplification group vs. 64.0% in the non-amplification group (P = 0.620).
Association between concentration or CNAs in cfDNA and treatment outcome
Patients who did not achieve disease control had significantly higher cfDNA levels than those who did; the median levels were 0.82 ng/μL (range, 0.28–6.42) and 0.82 ng/μL (range, 0.28–6.42) vs. 0.63 ng/μL (range, 0.13–15.0), respectively (P = 0.006) (Fig. 4a). The cfDNA-high group (above the median; n = 75) had a significantly lower DCR than the cfDNA-low group (n = 76) (52.0% [95% CI, 40.7–63.3%] vs. 75.0% [95% CI, 65.3–84.7%]; P = 0.003).
Similarly, patients who did not achieve disease control had significantly larger CNAs than those who did; the median I-scores were 3405 (range, 377–28,520) 1024 (range, 256–23,380), respectively (P = 0.0017) (Fig. 4b). The I-score-high group (above the median; n = 75) had a significantly lower DCR than the I-score-low group (n = 76) (49.3% [95% CI, 38.0–60.6%] vs. 77.6% [95% CI, 68.2–87.0%]; P = 0.0003).
The cfDNA-high group had significantly worse TTP and OS than the cfDNA-low group; the median TTP values were 2.2 months (95% CI, 1.4–2.9) and 4.1 months (95% CI, 4.0–4.3), respectively (HR = 1.71 [95% CI, 1.20–2.44]; P = 0.002) (Fig. 4c), and the median OS values were 4.1 months (95% CI, 3.6–4.6) and 14.8 months (95% CI, 8.1–21.6), respectively (HR = 3.50 [95% CI, 2.36–5.20]; P < 0.0001) (Fig. 4d). Similarly, TTP and OS were significantly worse in the I-score-high group than in the I-score-low group;; the median TTP values were 2.2 months (95% CI, 1.5–2.8) and 4.1 months (95% CI, 3.9–4.3), respectively (HR = 2.09 [95% CI, 1.46–3.00]; P < 0.0001) (Fig. 4e), and the median OS values were 4.6 months (95% CI, 3.6–5.6) and 14.8 months (95% CI, 8.5–21.2), respectively (HR = 3.35 [95% CI, 2.24–5.01]; P < 0.0001) (Fig. 4f). When patients were divided into quartile groups according to the I-score, the median TTP values were 2.3 months (95% CI, 0.7–3.8; HR = 2.3), 2.0 months (95% CI, 1.0–2.9; HR = 2.1), 4.1 months (95% CI, 2.9–5.3; HR = 1.3), and 4.3 months (95% CI, 3.7–4.9; HR = 1.0) (P = 0.0025) (Fig. 4g), and the median OS value were 4.1 months (95% CI, 3.3–5.0; HR = 5.0), 5.2 months (95% CI, 2.9–7.5; HR = 3.2), 11.2 months (95% CI, 4.3–18.2; HR = 1.5), and 18.4 months (95% CI; 11.3–25.6; HR = 1.0) (P < 0.0001), for the highest, second-highest, second-lowest, and lowest quartile, respectively (Fig. 4h).
In the multivariable analysis of TTP after adjusting for the baseline AFP level, which was also associated with TTP in the univariable analysis, the I-score retained independent prognostic value (Table 2). In a multivariable analysis for OS that included the baseline AFP level, macroscopic vascular invasion, cfDNA concentrations, and I-score, which were significant in the univariable analysis, the cfDNA concentration, I-score, and AFP level remained statistically significant prognostic factors (Table 3). Patients with a higher cfDNA concentration showed a 2.51-fold (95% CI, 1.62–3.89; P < 0.0001) increased risk of death compared with those with a lower cfDNA concentration. Likewise, patients with a higher I-score showed a 1.85-fold (95% CI, 1.16–2.96; P = 0.010) increased the risk of death compared with those with a lower I-score.
Among the three, representative, specific patients in Fig. 3, the patient with the highest I-score (28,520) (Fig. 3b) had the worst treatment outcomes (median TTP, 1.2 months; median OS, 3.5 months), the patient with a middle I-score (7448) (Fig. 3c) had intermediate outcomes (median TTP, 4.2 months; median OS, 11.0 months), and the patient with the lowest I-score (500) (Fig. 3d) had the best outcomes (median TTP, 26.3+ months; median OS, 26.6+ months).
Based on genomic profiling using comprehensive high-throughput technologies, various molecular classifications were proposed in HCC [16,17,18]. Some of these molecular classifications have prognostic significance by classifying patients into favorable versus unfavorable prognosis groups after surgery; however, none has become a tangible tool in the clinical decision process because of the lack of validation and the scarcity of tissue in HCC. Furthermore, it remains unknown whether molecular subclasses and their prognostic value in surgically resected cases are preserved in unresectable HCCs subjected to systemic treatment. Therefore, there is a need to develop molecular prognostic biomarkers for advanced HCC patients receiving systemic therapy that are easily measured and address spatial and temporal tumor heterogeneity.
Tumor cfDNA is increasingly used as a biomarker in various cancers because of its potential to identify genomic alterations in tumor tissues and track the genomic evolution of metastatic tumors [19, 20]. In the present study, high pretreatment cfDNA levels in plasma were significantly associated with poor outcomes in advanced HCC patients receiving sorafenib. Patients with a higher cfDNA concentration were less likely to achieve disease control and more likely to die than those with a lower cfDNA concentration. These findings are consistent with those of previous studies in metastatic breast, ovarian, or non-small cell lung cancers, or melanoma, [19, 21,22,23,24], whereas they are inconsistent with those in metastatic colorectal or non-small cell lung cancers [25, 26]. These contradictory results could be attributed to different systemic treatments or cut-off values for cfDNA levels in the different studies.
CNA refers to a form of genomic structural variation and includes gene amplification, gain, loss, and deletion. CNAs affect a larger fraction of the genome in cancers than any other type of somatic genetic alteration and play a key role in cancer development and progression [27,28,29]. Previous studies reported both large-scale and focal chromosomal alterations in HCC, with a high level of copy number changes in oncogenes and tumor suppressors, or genes implicated in core cancer pathways including cell cycle, p53, phosphoinositide 3-kinase, mitogen-activated protein kinase, Wnt, and transforming growth factor beta signaling [30, 31]. Given that CNAs could result in genomic instability and increased genomic instability is associated with poor prognosis in multiple cancer types [32, 33], increased CNA rates across the genome are likely to be associated with poor prognosis. In this study, large genome-wide CNAs in pretreatment cfDNA was a significant independent indicator of poor TTP and OS in HCC patients receiving sorafenib. Patients with larger CNAs, as represented by a higher I-score, were more likely to have disease progression or death than those with smaller CNAs. Weiss et al reported that CNAs in plasma cfDNA indicated by copy number instability (CNI) scores were significantly higher in patients with diverse advanced cancers than noncancer controls, and the decrease in CNI scores from baseline could predict the response to systemic chemotherapy, immunotherapy, or combinations of both [34, 35]. Carter et al showed that baseline copy number profiling in circulating tumor cells could be used to classify chemo-sensitive versus chemo-refractory small cell lung cancer . These results together with those of the present study suggest that CNAs in a liquid biopsy could serve as a prognostic or predictive indicator in advanced cancer patients receiving systemic therapy. However, since the present study was exploratory biomarker study with the exploratory nature of the analysis which also had a multiplicity issue, our study results should be validated in a well-designed prospective study with the appropriate statistical power for predefined endpoints.
To express genome-wide chromosomal instability, several scores such as CIN score , PA score , and S-score  were developed by the researchers. The CIN score was devised to measure the degree of CNAs across the entire genome of a tumor taking into account the total regions of the chromosome that are altered in a tumor as well as the amplitude of these alterations. The PA score was calculated as the number of SDs from the mean of the sum of the −log of the P values for the top five chromosome Z-scores of the 10 reference samples. S-score was calculated by the summation of all the squared Z-scores. The major difference between S-score and I-score is that I-score summates Z-scores which have more than 2 or less than − 2, not all the Z-scores. Many regions with Z-score less than 2 and more than − 2 can be detected in normal samples. However, by selection of highly deviated Z-scores in the I-score system, we could reflect definite cancer signals of ctDNA and reduce the noise which could occur during NGS experiments.
In addition to genome-wide CNA, we evaluated the association between VEGFA amplification in cfDNA and treatment outcomes based on a previous study suggesting VEGFA genomic amplification in HCC tumor tissues as a predictive biomarker for sorafenib [6, 8]. Although VEGFA copy number was significantly higher in HCC patients than in healthy controls, a significant association between VEGFA copy number and sorafenib treatment outcomes was not observed. However, since VEGFA amplification was evaluated only in part of the study population because of the limited quantity of blood sample in each patient, which could be a potential bias, further investigation is required to validate the predictive value of VEGFA amplification in HCC treated with sorafenib.
In conclusion, we demonstrated that pretreatment concentration and genome-wide CNAs in cfDNA are potential biomarkers predicting treatment outcomes in advanced HCC patients receiving first-line sorafenib.
Genome-wide copy number alteration
Copy number instability
Circulating tumor DNA
Disease control rate
Digital polymerase chain reaction
Response Evaluation Criteria In Solid Tumors
Time to progression
Vascular endothelial growth factor
Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J, Jemal A. Global cancer statistics, 2012. CA Cancer J Clin. 2015;65:87–108.
Altekruse SF1, Devesa SS, Dickie LA, McGlynn KA, Kleiner DE. Histological classification of liver and intrahepatic bile duct cancers in SEER registries. J Registry Manag 2011;38(4):201–205.
Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc JF, et al. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med. 2008;359:378–90.
Cheng AL, Kang YK, Chen Z, Tsao CJ, Qin S, Kim JS, et al. Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial. Lancet Oncol. 2009;10:25–34.
Llovet JM, Pena CE, Lathia CD, Shan M, Meinhardt G, Bruix J, et al. Plasma biomarkers as predictors of outcome in patients with advanced hepatocellular carcinoma. Clin Cancer Res. 2012;18:2290–300.
Horwitz E, Stein I, Andreozzi M, Nemeth J, Shoham A, Pappo O, et al. Human and mouse VEGFA-amplified hepatocellular carcinomas are highly sensitive to sorafenib treatment. Cancer Discov. 2014;4:730–43.
Bruix J, Cheng AL, Meinhardt G, Nakajima K, De Sanctis Y, Llovet J. Prognostic factors and predictors of sorafenib benefit in patients with hepatocellular carcinoma: Analysis of two phase III studies. J Hepatol. 2017;67(5):999–1008.
Luo X, Feng GS. VEGFA genomic amplification tailors treatment of HCCs with sorafenib. Cancer Discov. 2014;4:640–1.
Ono A, Fujimoto A, Yamamoto Y, Akamatsu S, Hiraga N, Imamura M, et al. Circulating tumor DNA analysis for liver cancers and its usefulness as a liquid biopsy. Cell Mol Gastroenterol Hepatol. 2015;1(5):516–34.
Tokuhisa Y, Iizuka N, Sakaida I, Moribe T, Fujita N, Miura T, et al. Circulating cell-free DNA as a predictive marker for distant metastasis of hepatitis C virus-related hepatocellular carcinoma. Br J Cancer. 2007;97:1399–403.
Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45:228–47.
Li H. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv Preprint. 2013; https://arxiv.org/abs/1303.3997v2. Accessed 26 May 2013.
Benjamini Y, Speed TP. Summarizing and correcting the GC content bias in high-throughput sequencing. Nucleic Acids Res. 2012. https://doi.org/10.1093/nar/gks001.
Beroukhim R, Getz G, Nghiemphu L, Barretina J, Hsueh T, Linhart D, et al. Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma. Proc Natl Acad Sci U S A. 2007;104(50):20007–12.
Cancer Genome Atlas Research Network. Electronic address: firstname.lastname@example.org, Cancer genome atlas research network. Comprehensive and integrative genomic characterization of hepatocellular carcinoma. Cell. 2017;41:169–1327 e23.
Lee JS, Chu IS, Heo J, Calvisi DF, Sun Z, Roskams T, et al. Classification and prediction of survival in hepatocellular carcinoma by gene expression profiling. Hepatology. 2004;40:667–76.
Chiang DY, Villanueva A, Hoshida Y, Peix J, Newell P, Minguez B, et al. Focal gains of VEGFA and molecular classification of hepatocellular carcinoma. Cancer Res. 2008;68:6779–88.
Zucman-Rossi J, Villanueva A, Nault JC, Llovet JM. Genetic landscape and biomarkers of hepatocellular carcinoma. Gastroenterology. 2015;149(5):1226–39 e4.
Dawson SJ, Tsui DW, Murtaza M, Biggs H, Rueda OM, Chin SF, et al. Analysis of circulating tumor DNA to monitor metastatic breast cancer. N Engl J Med. 2013;368:1199–209.
Murtaza M, Dawson SJ, Tsui DW, Gale D, Forshew T, Piskorz AM, et al. Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA. Nature. 2013;497:108–12.
Bidard FC, Madic J, Mariani P, Piperno-Neumann S, Rampanou A, Servois V, et al. Detection rate and prognostic value of circulating tumor cells and circulating tumor DNA in metastatic uveal melanoma. Int J Cancer. 2014;134:1207–13.
Lee JH, Long GV, Boyd S, Lo S, Menzies AM, Tembe V, et al. Circulating tumour DNA predicts response to anti-PD1 antibodies in metastatic melanoma. Ann Oncol. 2017;28:1130–6.
Nygaard AD, Holdgaard PC, Spindler KL, Pallisgaard N, Jakobsen A. The correlation between cell-free DNA and tumour burden was estimated by PET/CT in patients with advanced NSCLC. Br J Cancer. 2014;110:363–8.
Steffensen KD, Madsen CV, Andersen RF, Waldstrom M, Adimi P, Jakobsen A. Prognostic importance of cell-free DNA in chemotherapy resistant ovarian cancer treated with bevacizumab. Eur J Cancer. 2014;50:2611–8.
Tabernero J, Lenz HJ, Siena S, Sobrero A, Falcone A, Ychou M, et al. Analysis of circulating DNA and protein biomarkers to predict the clinical activity of regorafenib and assess prognosis in patients with metastatic colorectal cancer: a retrospective, exploratory analysis of the CORRECT trial. Lancet Oncol. 2015;16:937–48.
Li BT, Drilon A, Johnson ML, Hsu M, Sima CS, McGinn C, et al. A prospective study of total plasma cell-free DNA as a predictive biomarker for response to systemic therapy in patients with advanced non-small-cell lung cancers. Ann Oncol. 2016;27:154–9.
Beroukhim R, Mermel CH, Porter D, Wei G, Raychaudhuri S, Donovan J, et al. The landscape of somatic copy-number alteration across human cancers. Nature. 2010;463:899–905.
Kim TM, Xi R, Luquette LJ, Park RW, Johnson MD, Park PJ. Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes. Genome Res. 2013;23:217–27.
Zack TI, Schumacher SE, Carter SL, Cherniack AD, Saksena G, Tabak B, et al. Pan-cancer patterns of somatic copy number alteration. Nat Genet. 2013;45:1134–40.
Wang K, Lim HY, Shi S, Lee J, Deng S, Xie T, et al. Genomic landscape of copy number aberrations enables the identification of oncogenic drivers in hepatocellular carcinoma. Hepatology. 2013;58:706–17.
Chen CF, Hsu EC, Lin KT, Tu PH, Chang HW, Lin CH, et al. Overlapping high-resolution copy number alterations in cancer genomes identified putative cancer genes in hepatocellular carcinoma. Hepatology. 2010;52:1690–701.
Pinto AE, Pereira T, Santos M, Branco M, Dias A, Silva GL, et al. DNA ploidy is an independent predictor of survival in breast invasive ductal carcinoma: a long-term multivariate analysis of 393 patients. Ann Surg Oncol. 2013;20:1530–7.
Carter SL, Eklund AC, Kohane IS, Harris LN, Szallasi Z. A signature of chromosomal instability inferred from gene expression profiles predicts clinical outcome in multiple human cancers. Nat Genet. 2006;38:1043–8.
Weiss GJ, Beck J, Braun DP, Bornemann-Kolatzki K, Barilla H, Cubello R, et al. Changes in tumor cell-free DNA copy number instability (CNI) predict therapeutic response in metastatic cancers. Cancer Res. 2016. https://doi.org/10.1158/1538-7445.AM2016-3138.
Weiss GJ, Beck J, Braun DP, Bornemann-Kolatzki K, Barilla H, Cubello R, et al. Tumor cell-free DNA copy number instability predicts therapeutic response to immunotherapy. Clin Cancer Res. 2017;23:5074–81.
Carter L, Rothwell DG, Mesquita B, Smowton C, Leong HS, Fernandez-Gutierrez F, et al. Molecular analysis of circulating tumor cells identifies distinct copy-number profiles in patients with chemosensitive and chemorefractory small-cell lung cancer. Nat Med. 2017;23:114–9.
Leary RJ, Sausen M, Kinde I, Papadopoulos N, Carpten JD, Craig D, et al. Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing. Sci Transl Med. 2012;4(162):162ra154. https://doi.org/10.1126/scitranslmed.3004742.
Heitzer E, Ulz P, Belic J, Gutschi S, Quehenberger F, Fischereder K, et al. Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing. Genome Med. 2013;5(4):30.
Availability of data and material
This study was partially supported by a grant (2015–634) from the Asan Institute for Life Sciences, Asan Medical Center, Seoul, Republic of Korea. The funder had no role in the design of the study nor in the collection, analysis, and interpretation of data, nor in writing the manuscript.
Ethics approval and consent to participate
This prospective biomarker study was conducted under approval from the Institutional Review Board (IRB) at Asan Medical Center, Korea. All patients provided written informed consent before study enrollment.
Consent for publication
EHC, JHJ, and JL are employees of Genome Research Center, Green Cross Genome. All remaining authors declare no actual or potential conflicts of interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figure S1. Scatter plot demonstrating the correlation of the I-score with the total cell-free DNA concentration. Figure S2. Kaplan-Meier curves for (A) time to progression and (B) overall survival according to the VEGFA ratio. Abbraviation: VEGFA, vascular endothelial growth factor-A. (DOCX172 Kb)
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Oh, C.R., Kong, SY., Im, HS. et al. Genome-wide copy number alteration and VEGFA amplification of circulating cell-free DNA as a biomarker in advanced hepatocellular carcinoma patients treated with Sorafenib. BMC Cancer 19, 292 (2019). https://doi.org/10.1186/s12885-019-5483-x
- Hepatocellular carcinoma
- Circulating cell-free DNA
- Genome-wide copy number alteration
- Vascular endothelial growth factor-a