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Introduction

The treatment algorithm of the Asian Pacific Association for the Study of the Liver (APASL) recommends systemic therapy or best supportive care (BSC) for patients classified as Child-Pugh A/B or C with hepatocellular carcinoma (HCC) and extrahepatic metastasis, respectively (1). The European Association for the Study of the Liver (EASL) recommends systemic therapy or BSC for patients with cirrhosis with advanced- or terminal-stage HCC (2). The American Association for the Study of Liver Diseases (AASLD) recommends the use of systemic therapy over no therapy for patients with Child-Pugh A liver cirrhosis or for well-selected patients with Child-Pugh B liver cirrhosis plus advanced-stage HCC with macrovascular invasion and/or metastatic disease (3).

Although the multi-kinase inhibitors, sorafenib and lenvatinib, are approved first-line systemic treatments for unresectable HCC, treatment with atezolizumab [an anti-programmed death ligand-1 (PD-L1) monoclonal antibody] plus bevacizumab (an anti-vascular endothelial growth factor monoclonal antibody) (4) or tremelimumab (an anti-cytotoxic T-lymphocyte-associated antigen-4 monoclonal antibody) plus durvalumab (an anti-PD-L-1 monoclonal antibody) (5) is currently used as a first-line systemic therapy for patients with HCC classified as Child-Pugh A in Japan. In general, patients with unresectable HCC have a poor prognosis (6).

The long-term prognosis of elderly patients with HCC following hepatic resection is determined by the presence of liver cirrhosis and vascular invasion (7). Increased mortality following hepatectomy has been shown to be significantly associated with an older age (8). An older age and cardiac comorbidity have been shown to be significantly associated with radiofrequency ablation-related mortality (8). Another study demonstrated that the efficacy and safety of sorafenib did not differ significantly between younger and elderly patients with HCC (9). At present, researchers have not yet determined whether immune checkpoint inhibitor (ICI)-containing therapies, such as atezolizumab plus bevacizumab, are effective and safe for use in elderly patients with advanced-stage HCC (10,11). Treatment with ICIs can increase the risk of multi-organ autoimmune inflammatory responses, which are the most common type of complication associated with this type of treatment (12).

The present study reports the case of an elderly patient with unresectable advanced-stage HCC who received atezolizumab plus bevacizumab and achieved a complete response (CR) based on the modified Response Evaluation Criteria in Solid Tumors (mRECIST) (13,14).

Case report

A male patient in his 80s who consumed alcohol experienced body weight loss (-10 kg over a period of 6 months) in addition to appetite loss 2 months prior. He was regularly examined by a local doctor for hypertension or diabetes mellitus and was being treated with 10 mg empagliflozin, 5 mg linagliptin, 50 mg vildagliptin and 0.75 mg repaglinide daily, or 50 mg losartan potassium daily. The patient was subsequently introduced to Nihon University Itabashi Hospital (Tokyo, Japan) due to multiple liver tumors and suspected lung tumors in the right apex area.

Of note, 10 and 5 years prior, the patient had undergone cataract surgery and had spinal canal stenosis, respectively. In addition, 2 years prior to his admittance to the local hospital, he had received a transfusion for colonic diverticular bleeding. The patient did not have any tattoos or any history of drug abuse, and he consumed one cup of alcohol daily.

At the time of the first visit, the body length and body weight of the patient were 172 cm and 65 kg, respectively. His blood pressure, pulse rate, O2 saturation and body temperature were 169/67 mmHg, 62/min, 97% and 36.4˚C, respectively. He was conscious, his conjunctiva were not icteric or anemic, and liver tumors were palpable in the right hypochondriac region. No edema was observed on the feet. The Eastern Cooperative Oncology Group (ECOG) performance status score was 1 (PS-1).

The laboratory data from the first visit are presented in Table I and indicated mild abnormalities in liver function. The Child-Pugh score and grade were 5 and A, respectively. The albumin-bilirubin (ALBI) score was Grade 2a. Tests for both hepatitis B surface antigen and anti-hepatitis C virus antibodies yielded negative results. Although a history of hepatitis B virus (HBV) infection was suggested, serum HBV DNA was not detected. The α-fetoprotein (AFP) and lectin-reactive protein (AFP-L3) levels were elevated. Diabetes mellitus was well controlled.

Table I Laboratory data at the first visit of the patient to the hospital.

Table I

Laboratory data at the first visit of the patient to the hospital.

Items	Values	Items	Values
White blood cell counts	5,400/µl	Blood urea nitrogen	4.2 mg/dl
Hemoglobin	12.0 g/dl	Creatinine	1.12 mg/dl
Platelet counts	235,000/µl	eGFR	48.7 ml/min/1.73 m2
PT	93%	Glucose	102 mg/dl
INR	1.04	Hemoglobin A1c	6.4%
AST	85 IU/l	HBsAg	Negative
ALT	18 IU/l	anti-HBs	Positive
ALP	103 IU/l	anti-HBc	Positive
γ-GTP	690 IU/l	anti-HCV	Negative
Total bilirubin	0.42 mg/dl	ANA	<40
Total protein	6.8 g/dl	AFP	22,771 ng/ml
Albumin	3.7 g/dl	AFP-L3	66.0%
Total cholesterol	143 mg/dl	PIVKA-II	27 mAU/ml

[i] PT, prothrombin time; INR, international normalized ratio; AST, aspartate aminotransferase; ALT, alanine aminotransferase; ALP, alkaline phosphatase; γ-GTP, γ-glutamyl transpeptidase; eGFR, estimated glomerular filtration rate; HBsAg, hepatitis B surface antigen; anti-HBc, anti-hepatitis B core antibody; anti-HCV, anti-hepatitis C virus antibody; ANA, anti-nuclear antibody; AFP, α-fetoprotein; AFP-L3, lectin-reactive profile of AFP; PIVKA-II, protein induced by vitamin K absence or antagonist II.

A pre-treatment abdominal computed tomography (CT) scan demonstrated that 110 mm and other HCC nodules were present in segment 4 (S4), S5 and S8 of the liver, respectively. The P4 portal vein was disrupted, and swelling of the lymph nodes was observed in the paraaortic lesion and other sites (Fig. 1A-C).

Figure 1 Changes in abdominal CT scan images obtained during combination therapy with atezolizumab plus bevacizumab. (A-C) Prior to therapy, a CT scan demonstrated multiple hepatocellular carcinomas in the liver and swelling of the lymph nodes in the paraaortic lesion and other sites. (D-F) After 5 months of combination therapy, a CT scan demonstrated the disappearance of any intratumoral arterial enhancement in any of the target lesions. (G-I) At 4 months after the combination treatment was suspended, a CT scan did not demonstrate any recurrences. CT, computed tomography.

The patient was diagnosed with HCC stage IVA (15) and alcohol-associated liver cirrhosis with diabetes mellitus and hypertension. After screening for autoimmune diseases and/or the presence of high-risk esophageal varices, 1,200 mg atezolizumab (Tecentriq; Chugai Pharmaceutical Co., Ltd.) was administered intravenously, followed by 900 mg bevacizumab (Avastin; Chugai Pharmaceutical Co., Ltd.) every 3-4 weeks.

When unacceptable grade 2 or 3 adverse events developed, the combination therapy was suspended. Based on the mRECIST criteria (13,14), tumor assessment was performed by a contrast-enhanced CT scan every 1-2 months.

At 5 months following the commencement of the combination therapy, when six cycles of combination therapy were completed, the tumor marker levels of the patient returned to within normal limits: AFP, 1.8 ng/ml; AFP-L3, <0.5%; and protein induced by vitamin K absence or antagonist II (PIVKA-II), 17 mAU/ml (Fig. 2). A contrast-enhanced CT scan demonstrated the disappearance of any intratumoral arterial enhancement in any of the target lesions, indicating that the treatment response was complete (Fig. 1D-F). After 6 months of combination treatment with atezolizumab plus bevacizumab, the combination treatment was terminated due to the accidental occurrence of interstitial nephritis. The patient received steroid therapy and recovered.

Figure 2 Clinical course and changes in tumor markers in hepatocellular carcinoma in the case described herein. At 5 months after the commencement of combination therapy comprising atezolizumab and bevacizumab, the tumor marker levels of the patient returned to within normal limits. AFP, α-fetoprotein; AFP-L3, lectin-reactive profile of AFP; PIVKA-II, protein induced by vitamin K absence or antagonist II. The black arrows indicate the time points of single combination therapy with atezolizumab and bevacizumab.

When eight cycles of combination therapy were completed after 6 months of commencement, the patient terminated the combination therapy of atezolizumab plus bevacizumab due to his leg edema and renal dysfunction. His serum creatinine, albumin levels and estimated glomerular filtration rates (eGFR) were 1.86 mg/dl, 2.9 g/dl and 28 ml/min/1.73 m2, respectively. Urinary protein, urinary β2 microglobulin and urinary N-acetyl-beta-glucosaminidase levels increased [594 mg/dl (normal, <5 mg/dl), 886.4 µg/dl (normal, 5-200 µg/dl) and 14.8 U/l (normal, <5 U/l), respectively]. The patient was diagnosed with interstitial nephritis. In patients with chronic kidney diseases, the eGFR in those with grade 2 or 3 renal dysfunction is 30-59 ml/min/1.73 m2, or 15-30 ml/min/1.73 m2, respectively. The patient began to take 20 mg prednisolone (generic drug; oral route) daily, and his renal function gradually improved.

At 4 months after the combination treatment was suspended, no recurrences were observed (Fig. 1G-I). The patient's tumor marker levels remained within normal limits: AFP, 1.1 ng/ml; AFP-L3, <0.5%; and PIVKA-II, 11 mAU/ml. His serum creatinine, albumin levels and eGFR were 1.60 mg/dl, 2.9 g/dl and 32.9 ml/min/1.73 m2, respectively. His urinary protein level was 90 mg/dl. His leg edema disappeared although he still took 5 mg prednisolone daily. The authors plan to follow-up the patient carefully.

Discussion

The present study reports the case of a male patient in his 80s who consumed alcohol, with unresectable advanced-stage HCC who received atezolizumab plus bevacizumab for 6 months and achieved a CR. His performance status and Child-Pugh were ECOG PS-1 and grade A, respectively. The case described herein suggests that it is critical for patients with HCC and Child-Pugh A to continue therapy for HCC, even if they are older.

It has been demonstrated that in patients with unresectable HCC (median age, 64 years; range, 56-71 years), atezolizumab combined with bevacizumab results in improved overall and progression-free survival outcomes than sorafenib (4). Hosoda et al (16) reported successful multidisciplinary treatment with a CR to atezolizumab plus bevacizumab in a 90-year-old patient with HCC recurrence. Hatanaka et al (10) also reported that treatment with atezolizumab plus bevacizumab had an efficacy comparable to that of treatment with lenvatinib in HCC patients aged ≥80 years, and a CR was observed in 7.6% (7/92) of the patients.

ICI monotherapy or the immune-based combinations are associated with an improved survival, irrespective of the ECOG PS-0 or PS-1 status (17). HCC is one of the male-dominant cancers (18-20). Santoni et al (21) reported the sex difference in the efficacy of ICIs among cancer patients. However, further studies on this point are required among patients with HCC.

For the majority of patients with advanced-stage HCC, systemic therapy or BSC can be selected (1-3). A recent meta-analysis demonstrated that ICI therapy in the Child-Pugh B grade group was safe and was associated with a significant number of radiological responses, although survival outcomes were superior in the Child-Pugh A grade group (22). The development of more effective therapies is required for patients with advanced-stage HCC with a worse liver function than those with Child-Pugh A grade (23,24).

In case described in the present study, nephrotoxicity was observed during combination therapy with atezolizumab plus bevacizumab, although a renal biopsy was not performed. Nephrotoxicity, which can cause proteinuria, is one of the complications of both chemotherapy and immunotherapy (25-27).

Combination therapy comprising atezolizumab plus bevacizumab has been reported to be safe and widely effective (4,28,29). This combination may also play critical roles as systemic adjuvant treatment in HCC (30,31). Trans-arterial chemoembolization plus ICI may play a role in the treatment of patients with HCC (32).

In conclusion, as demonstrated in the present study, combination therapy comprising atezolizumab plus bevacizumab is effective for elderly patients with unresectable HCC. Careful attention should be paid to adverse events, including immune-related adverse events during and following combination treatment in elderly patients.

Acknowledgements

Not applicable.

Funding

Funding: No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Authors' contributions

SA and TK were major contributors to the conception and design of the study, as well as to the literature search for related studies. SA, TK, MT MH, SK, RST, NM, RM, HY, MO and HK observed the patient and examined his data. TK drafted the initial manuscript and revised the manuscript. All the authors have read and approved the final manuscript.

Ethics approval and consent to participate

The present study was conducted in accordance with the Declaration of Helsinki and was approved by the Ethics Committee of Nihon University Itabashi Hospital (protocol code: RK-180911-12; dates of approval: October 5, 2018 and September 13, 2023) for studies involving human participants. Participation in the study was posted on the website of Nihon University Itabashi Hospital (Tokyo, Japan), and informed consent was obtained from the patient described herein.

Patient consent for publication

Written informed consent was obtained from the patient for the publication of the present case report and any accompanying images.

Competing interests

The authors declare that they have no competing interests.

References