Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2011 Jan 17:11:4.
doi: 10.1186/1471-230X-11-4.

Complete response for advanced liver cancer during sorafenib therapy: case report

Affiliations
Case Reports

Complete response for advanced liver cancer during sorafenib therapy: case report

Rodolfo Sacco et al. BMC Gastroenterol. .

Abstract

Background: Hepatocellular carcinoma (HCC) is the fifth most common neoplasia in the world. In the past, treatment of advanced HCC with conventional antineoplastic drugs did not result in satisfactory outcomes: recently, in this patient population the oral multikinase inhibitor sorafenib has been able to induce a statistically significant improvement of overall survival. Similarly to other anti-angiogenic drugs employed in other tumour types, also sorafenib seldom induces the dimensional tumour shrinking usually observed with conventional cytotoxic drugs: data gathered from studies carried out with sorafenib and other competitors under development do not report any complete response in HCV-induced HCC.

Case presentation: An 84-year old man with a long-lasting history of chronic HCV hepatitis was referred to our Institution for an ultrasonography investigation of a focal hepatic lesion. To better characterize the liver disease and clearly define the diagnosis of the focal hepatic lesion, the patient was hospitalized in our department. Laboratory and instrumental investigations confirmed the clinical picture of HCV-related liver cirrhosis and identified a hepatic lesion of about 6 cm featuring infiltrating HCC with thrombosis of the portal trunk. Due to the advanced stage of the disease, therapy with sorafenib 400 mg bid was started. Right from one month after the treatment was started, a reduction of alpha-fetoprotein level was observed which, by the third month, turned down within the normal limits. In addition the CT scan showed 50% reduction of the neoplastic lesion along with canalization of the portal trunk. At the sixth month the normalization of the alpha-fetoprotein level at the lower limit of normality was confirmed and the MRI showed complete disappearance of the neoplasia. In addition a reduction of a metallo-proteinase serum level was observed. At the twelfth month a further MRI confirmed complete response had been maintained. At present the patient is in a follow-up program to evaluate the duration of the complete response.

Conclusions: This case is worth mentioning since, to the best of our knowledge, it represents the first evidence of complete response to sorafenib in an elderly patient with advanced HCV-related HCC.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Baseline CT examination: 1a, arterious phase; 1b, portal phase; 1c, late phase. Between III and IV hepatic segment is possible to observe the presence of a solid lesion with poorly defined margins and infiltrative nature; the lesion is hyperdense in arterial phase and hypodense in the portal phase and late, and it invades the left main portal vein which is thrombosed.
Figure 2
Figure 2
three-months follow-up with CT: 2a, arterious phase; 2b, portal phase; 2c, late phase. The three months CT scan document an apparent reduction in the size of lesion, which is associated with partial recanalization of the left portal branch.
Figure 3
Figure 3
Six months follow up with MRI before and after injection of Primovist: 3a, T1-weighted; 3b, T2-weighted; 3c, arterial phase; 3d, portal venous phase; e, hepatobiliary phase. At six months of treatment, the liver injury is no longer recognizable at MRI examination and the left portal branch is fully recanalized, as with almost complete response to treatment.
Figure 4
Figure 4
Twelve-months follow up with MRI before and after after injection of Primovist: 5a, T1-weighted; 5b, T2-weighted:On baseline T1w.i and T2w.i no sign of changes of signal intensity within the liver parenchyma is appreciable, not even at the level of the previous lesion of segment III.
Figure 5
Figure 5
Twelve-months follow up with MRI before and after after injection of Primovist: 6a, arterial phase; 6b portal venous phase; 6c portal venous phase delayed; 6d hepatobiliary phase. On post contrastographic dynamic study, there is no focal enhancement on arterial phase 6a, nor signs of portal branches invasion on portal venous phase 6b, nor areas of hypointensity on delayed phase 6c. On hepatobiliary phase 6d, homogeneous enhancement of the previous neoplastic parenchyma of segment III is now appreciable.
Figure 6
Figure 6
Analysis of metallo-proteinase 9 serum level: A clear reduction of marker serum level is observed after three months of treatment

References

    1. Parkin DM, Bray F, Ferlay J, Pisani P. Estimating the world cancer burden: GLOBOCAN 2000. Int J Cancer. 2001;94:153–156. doi: 10.1002/ijc.1440. - DOI - PubMed
    1. Mazzaferro V, Regalia E, Doci R. et al.Liver transplantation for the treatment of small Hepatocellular carcinomas in patients with cirrhosis. N Engl J Med. 1996;334:693–699. doi: 10.1056/NEJM199603143341104. - DOI - PubMed
    1. Bismuth H, Majno PE, Adam R. Liver transplantation for Hepatocellular carcinoma. Semin Liver Dis. 1999;19:311–322. doi: 10.1055/s-2007-1007120. - DOI - PubMed
    1. Jonas S, Bechstein WO, Steinmuller T. et al.Vascular invasion and histopathologic grading determine outcome after liver transplantation for Hepatocellular carcinoma in cirrhosis. Hepatology. 2001;33:1080–1086. doi: 10.1053/jhep.2001.23561. - DOI - PubMed
    1. Nowak AK, Chow PK, Findlay M. Systemic therapy for advanced hepatocellular carcinoma: A review. Eur J Cancer. 2004;40:1474–1484. doi: 10.1016/j.ejca.2004.02.027. - DOI - PubMed

Publication types