Liquid biopsy in esophageal cancer: a case report of false-positive circulating tumor DNA detection due to clonal hematopoiesis

Introduction

For patients with resectable locally advanced esophageal cancer, active surveillance after a clinically complete response to neoadjuvant chemoradiotherapy (nCRT) is currently being investigated as a novel treatment option (1-3). Limitations to organ-sparing approaches presently under investigation consist of a 10% risk of subclinical residual disease, and risk of patient non-compliance due to the high burden of invasive diagnostics (4,5). A promising new diagnostic approach in active surveillance is analysis of circulating tumor DNA (ctDNA). This involves detection of DNA fragments that enter the circulation by release from necrotic or apoptotic tumor tissue, or by active release from vital tumor cells (6). Tumor-specific genetic alterations can be identified in plasma-derived cell-free DNA (cfDNA) by next generation sequencing (NGS) (7-9). Ideally, residual or recurrent tumors after neoadjuvant treatment can be detected using these so-called “liquid biopsies”. For esophageal cancer, the application of liquid biopsies is still in its infancy. However, in some malignancies like non-small cell lung cancer and colorectal carcinoma it is already an accepted and valued modality for diagnosis of actionable mutations and detection of targeted treatment resistance mechanisms (10). Nevertheless, occasionally NGS of cfDNA yields mutations that cannot be matched with mutations found in tissue samples of the primary tumor. Hu et al. for example reported a series of thirty-three non-small cell lung cancer cases with a confirmed TP53 mutation in plasma genotyping of whom nineteen could not be identified in tumor biopsy (11). In that report, NGS of peripheral white blood cells reveals concordant somatic mutations within non-malignant hematopoietic cells associated with clonal hematopoiesis in five of these false-positive cases (12). Clonal hematopoiesis refers to clonal outgrowth of hematopoietic progenitor cells with somatic mutations. This phenomenon is not uncommon in the general population and affects 5–13% of people over 70 years old and 25% of cancer patients (12-15). White blood cells are the source of a significant proportion of circulating cfDNA (16). Therefore, clonal hematopoiesis potentially is a major factor in discordance between tumor genotyping and plasma cfDNA in not only non-small cell lung cancer, but other malignancies as well.

Herein we describe a patient with adenocarcinoma of the esophagogastric junction who underwent nCRT followed by surgical resection in whom genotyping of plasma cfDNA was discordant with matched tumor tissue due to clonal hematopoiesis. We present the following article in accordance with the CARE reporting checklist (available at https://dx.doi.org/10.21037/atm-21-525) (17).

Case presentation

A 66-year-old male was referred to our tertiary referral hospital in February 2016 (Figure 1). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient to perform comprehensive genomic testing and to publish his information. The patient had a medical history of gastroesophageal reflux disease and Barrett’s esophagus. He had no medical history of other malignancies. After standard diagnostic workup involving endoscopy with tumor biopsies plus endoscopic ultrasonography, diagnostic computed tomography (CT) and positron emission tomography with CT (PET-CT), the patient was diagnosed with cT3N0M0 (7^th ed. UICC TNM staging manual) adenocarcinoma of the gastroesophageal junction (t=0). NGS of tumor biopsies revealed a TP53 missense mutation (c.524G>A; p.R175H) with a variant allele frequency (VAF) of 71% (Table 1). The patient was initially treated with nCRT according to the ChemoRadiotherapy for Oesophageal cancer followed by Surgery Study (CROSS)-regimen (18). The patient participated in the preSANO trial, which aimed to assess the accuracy of diagnostic response evaluations after nCRT (5). In context of this trial, 14 weeks (t=2) as well as 21 weeks after baseline (t=3), post-nCRT endoscopy was performed during which no macroscopic tumor could be found. At these points in time, biopsies were taken of the tumor site, showing no residual tumor cells.

Figure 1 Timeline of events from baseline to death of the patient. cfDNA, cell-free DNA; nCRT, neoadjuvant chemoradiotherapy; CROSS, ChemoRadiotherapy for Oesophageal cancer followed by Surgery Study; CRE, clinical response evaluation; EGD, esophago-gastro-duodenoscopy; PET-CT, positron emission tomography plus computed tomography; EUS-FNA, endoscopic ultrasonography with fine-needle aspiration; TRG, tumor regression grade.

Table 1 Characteristics of next generation sequencing outcomes of resection specimens, tumor biopsies and cfDNA per point in time
Full table

Liquid biopsies were obtained at baseline (t=0) as well as 14 weeks after baseline (t=2; i.e., 8 weeks after completion of nCRT) and 21 weeks after baseline (t=3; i.e., 13 weeks after completion of nCRT). Analysis of cfDNA with Oncomine NGS at these points in time did not identify TP53 c.524G>A; p.R175H at baseline (t=0) and 14 weeks after baseline (t=2), in 3 or more independent molecules and a VAF of >0.1% (for 20 ng input). NGS did, however, consistently result in identification of a TP53 c.646G>A; p.V216M (VAF 0.37%, 0.34% and 0.32%, respectively) mutation. Twenty-two weeks after baseline (t=4; i.e., 14 weeks after completion of nCRT) the patient underwent a standard transhiatal esophagectomy. Resection specimen showed ypT1bN0 (all 19 removed lymph nodes negative) with Mandard’s Tumor Regression Grade 2 (1–10% residual vital tumor cells). The resection specimen did not contain sufficient residual tumor tissue for NGS.

Twenty-one months after initial diagnosis (t=5), biopsy from a solitary mass in the distal semimembranosus muscle revealed adenocarcinoma proving the patient had metastatic disease. Tissue mutation analysis revealed a TP53 c.524G>A; p.R175H mutation, confirming it being a metastasis from the forementioned esophageal carcinoma. The patient received palliative chemotherapy (t=6) with 6 cycles of intravenous paclitaxel and carboplatin. PET-CT imaging post-chemotherapy continued to show only this solitary soft tissue metastasis, therefore, the patient underwent surgical resection of this mass (t=7). Pathological analysis of metastatic tissue did not reveal remarkable mitotic activity. TP53 c.524G>A; p.R175H mutation again was identified after NGS of the resected metastasis. Twenty-seven months after baseline (t=8), during follow-up at the surgical outpatient clinic, liquid biopsies were obtained revealing TP53 c.646G>A; p.V216M (VAF 0.59%) mutation. The patient experienced a significant progression of symptoms 30 months after baseline (t=9) reporting pain, weight loss and malaise. Another set of liquid biopsies was obtained and at this point in time NGS identified TP53 c.524G>A; p.R175H (VAF 0.23%) as well as TP53 c.646G>A; p.V216M (VAF 0.86%) in cfDNA. Imaging studies showed a total of 12 skeletal- and soft-tissue metastases located in the vertebral column, the dorsal musculature, the pelvis and the bones and muscles of the right lower extremity (Figure 2). The patient received palliative treatment with analgesic medication and localized external beam radiation therapy on symptomatic bone metastases.

Figure 2 Variant allele frequency dynamics over time in cell-free DNA and white blood cells with corresponding PET-CT images. Images from left to right: baseline PET-CT image showing FDG-avid esophageal tumor; CRE-II (t=3) PET-CT image showing radiologically complete response to nCRT; PET-CT image at 21 months after baseline (t=5) showing FDG-avid lesion suspect for metastasis within the semimembranosus muscle; PET-CT image 26 months after baseline (t=7) of semimembranosus lesion showing decreased intensity after induction chemotherapy; PET-CT image 30 months after baseline (t=9) showing FDG-avid lesions suspect for metastasis within the adductor muscles of the right lower extremity, bilaterally in the pelvic acetabulum and in the transverse process of a thoracic vertebra. VAF, variant allele frequency; cfDNA, cell-free deoxyribonucleic acid; WBCs, white blood cells; PET-CT, positron emission tomography-computed tomography; nCRT, neoadjuvant chemoradiotherapy; FDG, 18-fluoride-fluorodeoxyglucose; CRE-II clinical response evaluation-II.

NGS of white blood cell DNA obtained at 30 months (t=9) and 33 months after baseline (t=10) revealed the presence of the TP53 c.646G>A; p.V216M mutation (VAF 0.77%), which was identical to the mutation consistently identified in previous plasma genotyping. Furthermore, a TP53 c.659A>G; p.Y220C mutation was identified in two independent white blood cell samples (Table 1). Analysis of cfDNA samples by droplet digital PCR (ddPCR) confirmed earlier results from NGS with Oncomine colon panel (Table 2). At the time of writing this report the patient has passed away, 46 months after initial diagnosis of esophageal cancer.

Table 2 Characteristics of ddPCR outcomes of cfDNA per point in time
Full table

Analyses

Blood samples drawn at t=0, t=2 and t=3 were collected using EDTA tubes. Plasma was separated, isolated and frozen within one hour after collection in order to provide stable cfDNA levels. All other samples were collected using CellSave tubes in which cfDNA levels are stable up to 96 hours after collection and were isolated and frozen within 48 hours (19). Isolation of cfDNA from plasma samples was performed with QIAamp Circulating Nucleic Acid kits (Qiagen, Hilden, Germany). DNA from white blood cells was extracted by a nucleospin kit. Concentrations of cfDNA were quantified using Quant-iT™ dsDNA High-Sensitivity Assay Kit (Thermo Fisher Scientific, Waltham, Massachusetts, USA) and Qubit^® 2.0 fluorometer (Thermo Fisher Scientific). Sequencing was performed on the Ion Torrent S5 GeneStudio Prime system (Thermo Fisher Scientific). Sequencing of tumor tissue DNA was completed using a dedicated custom-made cancer NGS panel for detection of TP53 aberrations. The entire coding region and the exon-intron boundaries of TP53 are covered by this panel. TP53 mutations in cfDNA of plasma samples were analyzed with cfDNA NGS kits with unique molecular identifiers (UMI: single molecule barcoding, Oncomine cfDNA assays, Thermo Fisher Scientific). Mean read coverage depths were >1,000 reads and >20,000 for diagnostic tissue and cfDNA NGS assays, respectively. In the cfDNA analysis identified variants were considered reliable when detected with at least 3 independent molecules (UMIs). To confirm our findings, tumor tissue DNA was also analyzed with Oncomine cfDNA assays and cfDNA in plasma samples were also analyzed using digital polymerase chain reaction (Crystal digital PCR, Stilla Technology, Villejuif, France).

Discussion

In this case report we describe the long-term follow-up of an esophageal carcinoma patient with false-positive plasma genotyping due to clonal hematopoiesis. In our patient a TP53 c.524G>A; p.R175H mutation was identified in the primary tumor via endoscopic biopsy. This is a well-described pathogenic variant associated with a variety of malignancies (20). Mutant p53 has been demonstrated to result in enhanced integrin and epidermal growth factor receptor (EGFR) trafficking causing increased cell scattering and invasion (21). Frequent plasma-derived cfDNA genotyping was performed aiming to find an association between disease activity and traceability of TP53 c.524G>A; p.R175H in plasma cfDNA. This mutation became detectable only after distant metastases had already been confirmed by clinical symptoms and standard imaging- and biopsy techniques. Surprisingly, plasma genotyping in our case consistently identified a TP53 c.646G>A; p.V216M mutation that was not found in the tumor tissues. TP53 c.646G>A; p.V216M variants have been associated with various malignancies. Although pathogenicity has as yet not been clearly established, it has been mentioned as a recurrent clonal hematopoietic variant (22,23). The VAF of the p.V216M variant was constant between baseline and 21 weeks while the patient developed a clinically complete response, which would suggest a clonal hematopoietic origin. Of interest, the VAF of TP53 c.646G>A; p.V216M doubled at 27 months and increased further at 30 months. This would have made it hard to ascribe it to clonal hematopoiesis if leukocyte analysis had not been performed. Eventual NGS of white blood cells identified this latter mutation in normal appearing white blood cells of the patient. Analysis of circulating tumor cells was performed which resulted in the finding of no epithelial cell adhesion molecule (EpCAM)-positive cells, rendering contamination of white blood cells by circulating tumor cells improbable and confirming the TP53 c.646G>A; p.V216M mutation was of clonal hematopoietic origin. In the present case-report we focused on TP53 mutation analysis.

Our case illustrates a number of challenges currently associated with cfDNA diagnostics in esophageal carcinoma. The tumor suppressor gene 53 (TP53) is one of the most frequently mutated genes in human cancers and codes for the p53 protein which has been referred to as “the guardian of the genome” (24,25). Esophageal adenocarcinoma displays an exceptionally high rate of TP53 mutations that reaches up to 70% (26). TP53, apart from frequently being altered in malignancy, is 1 out of 6 frequently mutated genes in clonal hematopoiesis as well (14). Over the past few years there has been an increased attention for clonal hematopoiesis. Acquisition of somatic mutations in hematopoietic cells results in abnormal clonal expansion that is associated with an increased risk of myeloid and lymphoid malignancies. Presence of clonal hematopoiesis in other types of malignancy is associated with worse outcomes and an increased risk of all-cause mortality (12). Clonal hematopoiesis is nevertheless most frequently a phenomenon of indeterminate malignant potential and can be found in 1 out of 10 people of 70 years and older and is present in a quarter of patients with any type of malignancy (13,14). This means that if cfDNA analysis in the future possibly becomes a diagnostic option in esophageal cancer, clinicians will have to consider the possibility of finding mutations that originate from clonal hematopoiesis rather than from a malignant lesion. This risk of false-positive test results can be readily averted by screening for clonal hematopoiesis in patients who have cfDNA mutations that cannot be matched with mutations in tumor biopsies.

NGS of cfDNA isolated from peripheral blood is a relatively new diagnostic modality that is already employed in a variety of cancers and has fueled great expectations of broad applicability. Application of this technique in active surveillance of esophageal carcinoma potentially replaces modalities such as endoscopy and PET-CT. This could have important benefits with regard to cost-effectiveness, invasiveness, and patient compliance. cfDNA analysis does however not yet capitalize on its potential value in the case we describe. Failure to detect TP53 c.524G>A; p.R175H in cfDNA is most likely due to the amount of ctDNA in the cfDNA fraction being below the limit of detection for NGS and ddPCR analyses. Recent data from esophageal carcinoma indicate that analysis using Cancer Personalized Profiling by deep sequencing (CAPP-seq, analysis of multiple tumor-specific DNA variants) can detect ctDNA down to 0.07%, well before tumor progression can be radiologically detected (27). Our case does however demonstrate the possibility of finding mutations originating from clonal hematopoiesis. We recommend correlation of mutations in cfDNA with mutations in tumor biopsies. If mutations in cfDNA cannot be matched with tumor mutations, performing NGS of white blood cells can confirm clonal hematopoiesis and preclude false-positive outcomes.

Acknowledgments

The authors thank Bo Noordman, Sjoerd Lagarde, Bianca Mostert for their contributions in obtainment of tissue- and blood samples and Ronald van Marion for his help with the NGS analyses. The authors would also like to acknowledge the contribution of Katharina Biermann in pathological analysis of the resection specimens.

Funding: None.

Footnote

Reporting Checklist: The authors have completed the CARE reporting checklist. Available at https://dx.doi.org/10.21037/atm-21-525

Peer Review File: Available at https://dx.doi.org/10.21037/atm-21-525

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://dx.doi.org/10.21037/atm-21-525). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient to perform comprehensive genomic testing and to publish his information.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

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