Oxaliplatin-induced hepatic sinusoidal obstruction syndrome in a patient with gastric cancer: A case report

Introduction

Gastric cancer is one of the leading causes of cancer-related mortality worldwide. Despite a decrease in its incidence in some regions of the world, gastric cancer remains a major clinical challenge as the majority of cases are diagnosed in an advanced stage, with a poor prognosis and limited treatment options (1). Oxaliplatin, a platinum-based antineoplastic agent, is used as an essential part of chemotherapeutic regimens for colorectal liver metastasis (2). Oxaliplatin-based regimens have been associated with the development of injury to the hepatic parenchyma in the form of hepatic sinusoidal obstruction syndrome (HSOS) (3–6). Since oxaliplatin-induced severe hepatic sinusoidal obstruction was first reported in 2004 (7), oxaliplatin-induced hepatic injury has become a major concern in patients with metastatic colorectal cancer (8–11). To the best of our knowledge, there have been no previously published reports on oxaliplatin-induced HSOS in other types of solid cancer. The present study described a case of oxaliplatin-induced HSOS in a patient with gastric cancer who received oxaliplatin-containing chemotherapy.

Case report

A 52-year-old man received gastroscopy because of dysphagia at Union hospital, Tongji Medical College (Wuhan, China) in Feb 2016. Gastroscopic examination indicated cardia-fundus neoplasia and pathological examination demonstrated gastric adnenocarcinoma. Subsequently, the patient underwent proximal gastrectomy for cardia-fundus gastric carcinoma and the pathological diagnosis was stage pT3N0M0 moderately and well-differentiated tubular adenocarcinoma. For treatment, the patient received five cycles of S-1 and oxaliplatin (SOX) regimen, consisting of intravenous injection of 130 mg/m2 oxaliplatin (Sanofi Pharmaceutical, Gentilly, France) on day 1 followed by oral administration of 50 mg TGOP capsules (50 mg tegafur, 14.5 mg gimeracil and 49 mg oteracil potassium; Qilu Pharmaceutical Co., Ltd., Jinan, China) twice daily on days 1–14, every 3 weeks. Following the five cycles of SOX, the patient presented no abnormal symptoms, and the results of blood routine examination and liver function tests were normal. The patient had no previous history of liver disease and denied alcohol use.

The patient received a general check-up before the sixth cycle of SOX on schedule. Peripheral blood routine examination results were as follows: White blood cells, 3.79×109 cells/l; red blood cells, 3.38×1012 cells/l; and platelet count, 179×109 cells/l. Liver function test results were as follows: Total bilirubin, 6.6 mmol/l; direct bilirubin, 4.4 mmol/l; alanine aminotransferase, 34 U/l (normal range, 21–72 U/l); aspartate aminotransferase, 55 U/l (normal range, 17–59 U/l); alkaline phosphatase, 190 U/l (normal range, 40–150 U/l); γ-glutamyl transferase, 58 U/l (normal range, 17–53 U/l); total protein, 64.9 g/l; and albumin, 32.1 g/l. Non-invasive fibrosis scores were as follows: Aspartate aminotransferase to platelet ratio index, 0.52; and fibrosis-4 score, 2.74. Tests for hepatitis A, B, C, and E, Epstein-Barr virus, and cytomegalovirus infection were negative. Anti-nuclear antibody was weak positive; other autoantibodies were negative; immunoglobulin G level (18.3 g/l; normal range, 7.51–15.6 g/l) was increased and other immunoglobulin levels were within the normal range.

Enlargement of the lymph nodes was not observed in the patient through physical examination and ultrasonography. Contrast-enhanced computed tomography (CT) revealed that liver parenchyma appeared heterogeneous and demonstrated predominantly moderate hypoattenuation in the left and right lobe of the liver (Fig. 1) (8). On dynamic contrast-enhanced magnetic resonance imaging (12), heterogeneous hypointensity was demonstrated in the portal-venous phase (Fig. 2). In addition, the patient received liver biopsy. Tissue sections (5-µm thick) were fixed in formalin at room temperature, and paraffin-embedded liver samples were stained at room temperature with hematoxylin and eosin for standard histological examination using a light microscope. Pathological examination indicated distinctive multifocal sinusoidal dilatation without piecemeal necrosis, hepatic rosette formation and emperipolesis (Fig. 3). Written informed consent was obtained from the patient prior to publication of the present case report.

Figure 1. Contrast-enhanced CT demonstrating heterogeneous hypoattenuation in the liver. (A) Pre-contrast, (B) artery phase, (C) portal phase and (D) hepatic venous phase images. Heterogeneous hypoattenuation (arrows) was demonstrated in the portal phase of contrast CT. CT, computed tomography.

Figure 2. Liver parenchyma with a heterogeneous and predominantly hypointense appearance on T1-weighted gadolinium-enhanced MRI. (A) Pre-contrast, (B) artery phase, (C) portal phase and (D) hepatic venous phase images. A heterogeneous hypointense appearance (arrows) was revealed on the portal phase of contrast-enhanced MRI. MRI, magnetic resonance imaging.

Figure 3. Pathological hematoxylin and eosin staining demonstrating distinctive sinusoidal dilatation (arrows) in the liver of a patient with gastric cancer who received oxaliplatin-containing chemotherapy (magnification, ×400).

Discussion

HSOS, also known as veno-occlusive disease, is an obliterative venulitis of the terminal hepatic venules (6). It occurs as a result of cytoreductive therapy prior to hematopoietic stem cell transplantation (HSCT), following oxaliplatin-containing chemotherapy for colorectal carcinoma metastatic to the liver, in patients taking pyrrolizidine alkaloid-containing herbal remedies (5,13,14). It is histologically characterized by sinusoidal dilatation, hepatocyte necrosis and obliterated hepatic venules due to damage to the sinusoidal endothelial cells (4). Sinusoidal changes induced by chemotherapeutic agents or pyrrolizidine alkaloid-containing herbals are caused by a direct toxicity to sinusoidal endothelial cells (12). In addition, toxic agents have an adverse effect on bone marrow progenitors of endothelial cells that are responsible for the repair of sinusoidal lesions (15). The clinical presentations of HSOS include jaundice, right upper-quadrant pain and tender hepatomegaly, ascites and unexplained weight gain. The diagnosis of a HSOS result from HSCT or pyrrolizidine alkaloid (PA)-containing herbals is based on a history of taking PAs-containing herbs and a classical triad of weight gain, painful hepatomegaly and jaundice (13,14). However, clinical manifestations of the patients with oxaliplatin-induced HSOS appear to be mild or absent (10). Thus, it is challenge to define HSOS in patients who have received oxaliplatin-contained chemotherapy. Notably, patients with oxaliplatin-induced HSOS may give rise to elevated morbidity rates and increased bleeding risk. Thus, it is important to identify HSOS in patients who receive oxaliplatin-contained chemotherapy.

The diagnosis of HSOS is established by histological examination; however, the patchy nature of HSOS incurs sampling variability that confines the diagnostic yield of the biopsy. Previous studies have demonstrated that CT and/or MRI scans may provide excellent strategies for the screening of oxaliplatin-induced HSOS (8,10,11,16). In the present study, heterogeneous and predominantly hypoattenuation of the hepatic parenchyma was a distinctive radiological sign of oxaliplatin-induced HSOS on the CT scan. In addition, reticular hypointensity was an important indicator of oxaliplatin-induced HSOS observed from MRI in the patient. These imaging signs were also reported in previous studies (8,10,11,16). Notably, various studies have demonstrated that oxaliplatin-induced HSOS manifested as focal liver lesions and mimicked metastatic colon cancer in the liver (17,18). Thus, HSOS should have been differentiated from metastatic gastric cancer. Details of history, careful observation of radiological findings, and histological examination provide assistance in distinguishing oxaliplatin-induced HSOS from metastatic cancer.

In conclusion, the present case report detailed oxaliplatin-induced HSOS in a patient with gastric cancer. HSOS should be considered as one of the potential causes of newly-developed hepatic lesions in patients with gastric cancer who receive oxaliplatin. The present case highlights that oxaliplatin may induce HSOS not only in metastatic colon cancer in the liver, but also in other types of cancer, such as gastric cancer. Further studies are required to identify characteristics that predispose individuals to HSOS secondary to oxaliplatin and the prognosis of oxaliplatin-induced HSOS in gastric cancer.

Acknowledgments

The present study was supported by the National Natural Science Foundation of China (grant nos. 81570555 and 81270506).

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