Long‑term follow‑up of complete remission of advanced hepatocellular carcinoma following sorafenib therapy: A case report

Introduction

Hepatocellular carcinoma (HCC) is the third-leading cause of cancer-associated mortality worldwide, accounting for more than 600,000 deaths per year (1). A large proportion of these patients are not candidates for potentially curative therapy, including surgical resection, liver transplantation or local ablation therapy, as they are diagnosed with advanced disease with vascular invasion and/or distant metastasis (2,3). Sorafenib is a multi-kinase inhibitor, which inhibits a number of kinase-dependent signaling pathways associated with tumor progression and angiogenesis, including those involving Raf serine/threonine kinase, vascular endothelial growth factor receptor (VEGFR)-2, VEGFR-3, and platelet-derived growth factor β-receptor (4,5). The efficacy of sorafenib was demonstrated in two large phase III clinical trials including the Sorafenib HCC Assessment Randomized Protocol (SHARP) trial and the Asia-Pacific trial (conducted in the Asia-Pacific region) (6,7). Although there was a survival benefit for patients with advanced HCC, only a limited number of patients demonstrated a partial response, and there were no cases of complete remission (CR). Furthermore, the marginal observed survival gain of 2.8 months in the SHARP trial and 2.3 months in the Asia-Pacific trial did not meet the expectations of clinical practice. Following the approval of sorafenib, several cases of CR subsequent to sorafenib therapy were reported worldwide (8–11). However, there is little data regarding the clinical course and safety of long-term sorafenib therapy in cases of CR. Therefore, the present study reports a case of long-term maintenance therapy with sorafenib following the achievement of CR in a patient with advanced HCC.

Case report

A 72-year-old male patient was referred for the evaluation of a liver mass identified on an abdominal ultrasound performed for routine health screening purposes. The patient was taking medications for diabetes, hypertension and an old cerebral infarction. Initial laboratory results were as follows: White blood cells 5,920/mm3 (normal range, 4–10×103/mm3), hemoglobin level 14.0 g/dl (normal range, 12–16 g/dl), platelet count 237×103/mm3 (normal range, 100–300×103/mm3), alanine aminotransferase (ALT) 29 IU/l (normal range, 0–40 IU/l), total bilirubin 1.0 mg/dl (normal range, 0.1–1.1 mg/dl), albumin 3.9 mg/dl (normal range, 4.0–5.5 mg/dl) and prothrombin time 11.6 sec (normal range, 10.4–13.3 sec). With regard to virological markers, the patient was positive for hepatitis C virus antibody and negative for hepatitis B surface antigen. The serum α-fetoprotein (AFP) level and protein induced by vitamin K absence or antagonist-II level were 60,500 ng/ml (normal range, 0–1 ng/ml) and 2,000 mAU/ml (normal range, 0–40 mAU/ml), respectively. Baseline electrocardiography (ECG) and echocardiography revealed normal left ventricular systolic function (left ventricular ejection fraction, 65%) with normal sinus rhythm. Multiphasic computed tomography (CT) scans of the abdomen demonstrated a huge, 13 cm-sized mass replacing the right lobe of the liver, with portal vein thrombosis (Fig. 1A). HCC was confirmed by ultrasound-guided percutaneous needle biopsy of the liver mass (Fig. 2). The cancer was staged as advanced HCC according to the Barcelona Clinic Liver Cancer staging system (12) and the patient's Eastern Cooperative Oncology Group performance status (13) was 1; the patient was treated with 400 mg sorafenib (Nexavar; Bayer AG, Leverkusen, Germany) twice daily. Following the initiation of sorafenib therapy, the patient experienced a grade 1 (14) hand-foot skin reaction, which was well tolerated without requiring a dose reduction.

Figure 1. Multiphasic contrast-enhanced CT of the abdomen. (A) Initial abdominal CT scan demonstrated a 13-cm mass with arterial enhancement and early wash-out accompanying tumor thrombus of the portal vein in segment 5 and 6; (B) Following 4 months of sorafenib therapy, CT scans revealed the disappearance of the enhanced mass and recanalization of the portal vein; (C) At the 52 months-follow-up, CT scans demonstrated the further decrease of a non-enhanced mass with a patent portal vein. CT, computed tomography.

Figure 2. Percutaneous liver biopsy confirmed an Edmondson-Steiner grade III hepatocellular carcinoma featuring a trabecular pattern. (A) HE staining; magnification, ×100; (B) HE staining; magnification, ×200. HE, hematoxylin and eosin.

After 40 days of sorafenib therapy, the tumor size had decreased to 6 cm and the serum AFP level had decreased to 571 ng/ml. The follow-up abdominal CT scans at 4 months demonstrated no enhancing viable lesions in the tumor and recanalization of the portal vein; additionally, serum AFP values normalized (8.42 ng/ml; Fig. 1B). The sorafenib dose was maintained at 400 mg twice daily for 16 months, after which the sorafenib dose was reduced to 400 mg a day due to the elevation of serum ALT (231 IU/ml). Sorafenib therapy was continued for 48 months until the patient experienced dyspnea due to congestive heart failure with pleural effusion (Fig. 3). An echocardiogram revealed decreased left ventricular systolic function (left ventricular ejection fraction, 40%), including new-onset atrial fibrillation on the follow-up ECG. Following the discontinuation of sorafenib and the addition of rate control medication, the patient's dyspnea improved, with the disappearance of the pleural effusion. Without sorafenib therapy, the patient remained in a state of CR, followed up with serial CT scans and tumor marker measurement, for 52 months from the time of initiation of the sorafenib therapy (Fig. 1C). Written informed consent was obtained from the patient for the publication of their clinical data and images.

Figure 3. Following 44 months of sorafenib therapy, a follow-up chest x-ray revealed an increase of the pulmonary vascular marking and cardio-thoracic ratio, with left pleural effusion. (A) Initial chest x-ray; (B) Chest x-ray from the 44 month follow-up.

Discussion

At present, sorafenib is the only chemotherapeutic agent that has been proven to increase overall survival time in patients with advanced HCC (6,7). Although partial response was achieved in only 2 and 3.3% of patients in two large phase III clinical trials, with no cases of CR (6,7), there have been several reports of CR following sorafenib therapy in patients with advanced HCC since sorafenib became available for general clinical practice (8–11). The majority of CR cases exhibited early tumor response following sorafenib therapy accompanied by a rapid radiological response and the normalization of AFP within 6 months of sorafenib therapy (8–11). In accord with previous reports, the present case exhibited a similar clinical course, including a rapid radiologic response and the normalization of serum AFP within 40 days of sorafenib therapy (Fig. 4). Early AFP response following the initiation of sorafenib therapy has previously been identified as a positive prognostic factor for patients with advanced HCC (15). Further investigation regarding the contributing factors and molecular pathophysiology of these sorafenib responders is required.

Figure 4. Clinical course and alteration of serum AFP level and tumor size based on RECIST and mRECIST. AFP, α-fetoprotein; RECIST, response evaluation criteria in solid tumor; mRECIST, modified response evaluation criteria in solid tumor; ALT, alanine aminotransferase; EF, ejection fraction.

Although CR cases following sorafenib therapy have been reported in the literature, there is limited data regarding the long-term clinical course of these cases following the achievement of CR (8–11). Therefore, there is no consensus on a management strategy for CR-achieving patients. As in the present case, if the patient can tolerate sorafenib therapy, long-term sorafenib therapy may be an option as a maintenance treatment following CR. However, in addition to the economic burden of continuing sorafenib, there is limited data on safety profiles in regard to long-term sorafenib therapy (16,17). As it targets multiple angiogenic receptors, sorafenib causes a unique spectrum of adverse events including skin rash, stomatitis and cardiovascular toxicity. During sorafenib therapy, cardiovascular adverse events, including hypertension, bleeding and cardiac or cerebrovascular events were among the most serious observed in clinical trials (6). Among these cardiovascular toxicities, hypertension and bleeding are most frequent adverse events associated with sorafenib therapy (18). Although there have been reports of cardiotoxicity from the long-term sorafenib therapy of patients with renal cell cancer and lung cancer, the present case is the first report of cardiotoxicity caused by long-term sorafenib therapy in a patient with advanced HCC; this adverse effect has been underestimated by phase III studies due to the relatively short-term treatment (19,20). The present case encourages the clinician to monitor cardiac toxicity during sorafenib therapy, particularly in elderly patients with underlying cardiovascular diseases.

Compared with the literature to date, the present case represents an HCC case with the longest follow-up subsequent to CR induced by sorafenib therapy. Although the therapeutic response was assessed by radiologic findings, rather than by pathologic confirmation, CR was confirmed by long-term sustained radiologic response with a normal AFP level, even subsequent to the termination of sorafenib therapy. The present case provides the valuable insight that long-term sorafenib therapy may be an option subsequent to achieving CR through treatment with sorafenib, and that efforts should be made to monitor for the appearance of less common adverse events in patients receiving long-term sorafenib therapy.

Acknowledgements

The present study was supported by the Kyungpook National University Research Fund, 2010 (grant no., 201014100000).

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