|Classification and external resources|
Liver cancer or hepatic cancer (from the Greek hēpar, meaning liver) is a cancer that originates in the liver. Liver tumors are discovered on medical imaging equipment (often by accident) or present themselves symptomatically as an abdominal mass, abdominal pain, yellow skin, nausea or liver dysfunction.
The leading cause of liver cancer is viral infection with hepatitis B virus or hepatitis C virus. The cancer usually forms secondary to cirrhosis caused by these viruses. For this reason, the highest rates of liver cancer occur where these viruses are endemic, including East-Asia and sub-Saharan Africa. Liver cancers should not be confused with liver metastases, also known as secondary liver cancer, which are cancers that originate from organs elsewhere in the body and migrate to the liver. They are formed from either the liver itself or from structures within the liver, including blood vessels or the bile duct. Five year survival rates are 17% in the United States.
- 1 Classification
- 2 Signs and symptoms
- 3 Causes
- 4 Diagnosis
- 5 Prevention
- 6 Treatment
- 7 Epidemiology
- 8 Research
- 9 References
- 10 External links
The most frequent liver cancer, accounting for approximately 75% of all primary liver cancers, is hepatocellular carcinoma (HCC) (also named hepatoma, which is a misnomer because adenomas are usually benign). HCC is a cancer formed by liver cells, known as hepatocytes, that become malignant. Another type of cancer formed by liver cells is hepatoblastoma, which is specifically formed by immature liver cells. It is a rare malignant tumor that primarily develops in children, and accounts for approximately 1% of all cancers in children and 79% of all primary liver cancers under the age of 15. Most of these tumors form in the right lobe.
Liver cancer can also form from other structures within the liver such as the bile duct, blood vessels and immune cells. Cancer of the bile duct (cholangiocarcinoma and cholangiocellular cystadenocarcinoma) account for approximately 6% of primary liver cancers. There is also a variant type of HCC that consists of both HCC and cholangiocarcinoma. Tumors of the blood vessels (angiosarcoma and hemangioendothelioma, embryonal sarcoma and fibrosarcoma are produced from a type of connective tissue known as mesenchyme. Cancers produced from muscle in the liver are leiomyosarcoma and rhabdomyosarcoma. Other less common liver cancers include carcinosarcomas, teratomas, yolk sac tumours, carcinoid tumours and lymphomas. Lymphomas usually have diffuse infiltration to liver, but It may also form a liver mass in rare occasions.
Many cancers found within the liver are not true liver cancers, but are cancers from other sites in the body that have spread to the liver (known as metastases). Frequently, the site of origin is the gastrointestinal tract (such as colon cancer and carcinoid tumors mainly of the appendix), but also from breast cancer, ovarian cancer, lung cancer, renal cancer, prostate cancer.
Signs and symptoms
Because liver cancer is an umbrella term for many types of cancer, the signs and symptoms depend on what type of cancer is present. Cholangiocarcinoma is associated with sweating, jaundice, abdominal pain, weight loss and hepatomegaly. Hepatocellular carcinoma is associated with abdominal mass, abdominal pain, emesis, anemia, back pain, jaundice, itching, weight loss and fever.
Viral infection with either hepatitis C virus (HCV) or Hepatitis B virus (HBV) is the primary cause of liver cancer, accounting for 80% of hepatocellular carcinoma (HCC). The viruses cause HCC because massive inflammation, fibrosis and eventual cirrhosis occurs within the liver. HCC usually arises after cirrhosis, with an annual incidence of 1.7% in cirrhotic HCV-infected individuals. Around 5-10% of individuals that become infected with HBV become chronic carriers, and around 30% of these acquire chronic liver disease, which can lead to HCC. HBV infection is also linked to cholangiocarcinoma. The role of viruses other than HCV or HBV in liver cancer is much less clear, although there is some evidence that co-infection of HBV and hepatitis D virus may increase the risk of HCC.
Many genetic and epigenetic changes are formed in liver cells during HCV and HBV infection, which is a major factor in the production of the liver tumours. The viruses promote malignant characteristics of cells by altering gene methylation, affecting gene expression and promoting or repressing cellular signal transduction pathways. By doing this the viruses can prevent cells from undergoing a programmed form of cell death (apoptosis) and promote viral replication and persistence.
In addition to virus-related cirrhosis described above, other causes of cirrhosis can lead to HCC. Alcohol intake correlates with risk of HCC, and the risk is far greater in individuals with an alcohol-induced cirrhotic liver. There are a few disorders that are known cause cirrhosis and lead to cancer, including hereditary hemochromatosis and primary biliary cirrhosis.
Aflatoxin exposure can lead to the development of HCC. The aflatoxins are a group of chemicals produced by the fungi Aspergillus flavus (the name comes from A. flavus toxin) and A. parasiticus. Food contamination by the fungi leads to ingestion of the chemicals, which are very toxic to the liver. Common foodstuffs contaminated with the toxins are cereals, peanuts and other vegetables. Contamination of food is common in Africa, South-East Asia and China. HBV infection and aflatoxin exposure increases the risk to over three times that seen in HBV infected individuals without exposure. The mechanism by which aflatoxins cause cancer is through genetic mutation of a gene required for the prevention of cancer: p53.
Other causes in adults
- High grade dysplastic nodules are precancerous lesions of the liver. Within 2 years, there is a risk of cancer arising from these nodules of 30-40%.
- Obesity has emerged as an important risk factor as it can lead to steatohepatitis.
- Diabetes increases the risk of HCC.
- Smoking increases the risk of HCC compared to non-smokers and previous smokers.
- There is around 5-10% lifetime risk of cholangiocarcinoma in people with Primary sclerosing cholangitis.
- Liver fluke infection increases the risk of cholangiocarcinoma, and is the reason Thailand has particularly high rates of this cancer.
Risk factors in children
Increased risk of liver cancer in children can be caused by Beckwith-Wiedemann Syndrome (associated with hepatoblastoma), familial adenomatous polyposis (associated with hepatoblastoma), low birth weight (associated with hepatoblastoma), Progressive familial intrahepatic cholestasis (associated with HCC) and Trisomy 18 (associated with hepatoblastoma).
Many imaging modalities are used to aid in the diagnosis of primary liver cancer. For HCC these include sonography (ultrasound), computed tomography (CT) and magnetic resonance imaging (MRI). Positron emission tomography (PET) is commonly used for imaging cancers by detecting cells with high metabolic rates; a common feature of cancer cells. In HCC, PET has little effectiveness due to the high metabolic activity of normal liver cells. When imaging the liver with ultrasound, a mass greater than 2 cm has more than 95% chance of being HCC. The majority of cholangiocarcimas occur in the hilar region of the liver, and often present as bile duct obstruction. If the cause of obstruction is suspected to be malignant, endoscopic retrograde cholangiopancreatography (ERCP), ultrasound, CT, MRI and magnetic resonance cholangiopancreatography (MRCP) are used.
Tumor markers, chemicals sometimes found in blood of people with cancer, can be used to diagnose liver cancers. High levels of alpha-fetoprotein (AFP) in the blood can be found in many cases of HCC and intrahepatic cholangiocarcinoma. Cholangiocarcinoma can be detected with the commonly used tumor makers; carbohydrate antigen 19-9 (CA 19-9), carcinoembryonic antigen (CEA) and cancer antigen 125 (CA125). Although these tumour markers are found in primary liver cancers, they are also found in cancer and other disorders.
Prevention of cancers can be separated into primary, secondary and tertiary prevention. Primary prevention preemptively reduces exposure to a risk factor for liver cancer. One of the most successful primary liver cancer preventions is vaccination against hepatitis B. Vaccination for hepatitis C virus is currently unavailable. Other forms of primary prevention are aimed at limiting transmission of these viruses by promotion of safe injection practice, screening of blood donation products and screening of high risk asymptomatic individuals. Aflatoxin exposure can be avoided by post-harvest intervention, which has been effective in west Africa. Reducing alcohol abuse, obesity, and diabetes would also reduce rates of liver cancer. Diet control in hemochromatosis could decrease the risk of iron overload, decreasing the risk of cancer.
Secondary prevention includes both cure of the agent involved in the formation of cancer (carcinogenesis) and the prevention of carcinogenesis if this is not possible. Cure of virus-infected individuals is not possible, but treatment with antiviral drugs such as interferon can decrease the risk of liver cancer. Chlorophyllin may have potential in reducing the effects of aflatoxin.
Tertiary prevention includes treatments to prevent the recurrence of liver cancer. These include the use of chemotherapy drugs, and antiviral drugs.
Surgical resection is often the treatment of choice for non-cirrhotic livers. Increased risk of complications such as liver failure can occur with resection of cirrhotic livers. 5-year survival rates after resection has massively improved over the last few decades and can now exceed 50%. Recurrence rates after resection due to the spread of the initial tumor or formation of new tumors exceeds 70%. Liver transplantation can also be used in cases of HCC where this form of treatment can be tolerated and the tumor fits specific criteria (such as the Milan criteria). Less than 30-40% of individuals with HCC are eligible for surgery and transplant because the cancer is often detected late stage. Also, HCC can progress during the waiting time for liver transplants, which can prevent transplant due to the strict criteria.
Percutaneous ablation is the only non-surgical treatment that can offer cure. There are many forms of percutaneous ablation, which consist of either injecting chemicals into the liver (ethanol or acetic acid) or producing extremes of temperature using radio frequency ablation, microwaves, lasers or cryotherapy. Of these, radio frequency ablation has one of the best reputations in HCC, but the limitations include inability to treat tumors close to other organs and blood vessels due to heat generation and the heat sync effect, respectively.
Systemic chemotherapeutics are not routinely used in HCC, although local chemotherapy may be used in a procedure known as transarterial chemoembolization. In this procedure, cytotoxic drugs such as doxorubicin or cisplatin with lipiodol are administered and the arteries supplying the liver are blocked by gelatin sponge or other particles. Because most systemic drugs have no efficacy in the treatment of HCC, research into the molecular pathways involved in the production of liver cancer produced Sorafenib, a targeted therapy drug that prevents cell proliferation and blood cell growth. This drug provides a survival benefit for advanced HCC.
Radiotherapy is not often used in HCC because the liver is not tolerant to radiation. Although with modern technology it is possible to provide well targeted radiation to the tumor, minimizing the dose to the rest of the tumor. Dual treatments of radiotherapy plus chemoembolization, local chemotherapy, systemic chemotherapy or targeted therapy drugs may show benefit over radiotherapy alone.
Resection is an option in cholangiocarcinoma, but less than 30% of cases of cholangiocarcinoma are resectable at diagnosis. After surgery, recurrence rates are up to 60%. Liver transplant may be used where partial resection is not an option, and adjuvant chemoradiation may benefit some cases.
60% of cholangiocarcinomas form in the perihilar region and photodynamic therapy can be used to improve quality of life and survival time in these cases. Photodynamic therapy is a novel treatment that utilitizes light activated molecules to treat the tumor. The compounds are activated in the tumor region by laser light, which causes the release of toxic reactive oxygen species, killing tumor cells.
Removing the tumor by either surgical resection or liver transplant can be used in the treatment of hepatoblastoma. In some cases surgery can offer a cure. Chemotherapy may be used before and after surgery and transplant.
Chemotherapy, including cisplatin, vincristine, cyclophosphamide, and doxorubicin are used for the systemic treatment of hepatoblastoma. Out of these drugs, cisplatin seems to be the most effective.
Globally, as of 2010[update], liver cancer resulted in 754,000 deaths, up from 460,000 in 1990, making it the third leading cause of cancer death after lung and stomach. In 2012, it represented 7% of cancer diagnoses in men, the 5th most diagnosed cancer that year. Of these deaths 340,000 were secondary to hepatitis B, 196,000 were secondary to hepatitis C, and 150,000 were secondary to alcohol. HCC, the most common form of liver cancer, shows a striking geographical distribution. China has 50% of HCC cases globally, and more than 80% of total cases occur in sub-Saharan Africa or in East-Asia due to hepatitis B virus. Cholangiocarcinoma also has a significant geographical distribution, with Thailand showing the highest rates worldwide due to the presence of liver fluke.
Liver cancer is the eighteenth most common cancer in the UK (round 4,300 people were diagnosed with liver cancer in the UK in 2011), and it is the twelfth most common cause of cancer death (around 4,500 people died of the disease in 2012).
- Jemal, A; Bray, F; Center, MM; Ferlay, J; Ward, E; Forman, D (Mar–Apr 2011). "Global cancer statistics.". CA: a cancer journal for clinicians 61 (2): 69–90. doi:10.3322/caac.20107. PMID 21296855.
- "SEER Stat Fact Sheets: Liver and Intrahepatic Bile Duct Cancer". NCI. Retrieved 18 June 2014.
- World Cancer Report 2014. World Health Organization. 2014. pp. Chapter 1.1. ISBN 9283204298.
- Ahmed, Ahmed, I; Lobo D.N.; Lobo, Dileep N. (January 2009). "Malignant tumours of the liver". Surgery (Oxford) 27 (1): 30–37. doi:10.1016/j.mpsur.2008.12.005.
- Emre, S; McKenna, GJ (December 2004). "Liver tumors in children.". Pediatric transplantation 8 (6): 632–8. doi:10.1111/j.1399-3046.2004.00268.x. PMID 15598339.
- Khan, SA; Davidson, BR; Goldin, RD; Heaton, N; Karani, J; Pereira, SP; Rosenberg, WM; Tait, P; Taylor-Robinson, SD; Thillainayagam, AV; Thomas, HC; Wasan, H; British Society of, Gastroenterology (December 2012). "Guidelines for the diagnosis and treatment of cholangiocarcinoma: an update". Gut 61 (12): 1657–69. doi:10.1136/gutjnl-2011-301748. PMID 22895392.
- Arzumanyan, A; Reis, HM; Feitelson, MA (February 2013). "Pathogenic mechanisms in HBV- and HCV-associated hepatocellular carcinoma.". Nature reviews. Cancer 13 (2): 123–35. doi:10.1038/nrc3449. PMID 23344543.
- Rosen, HR (Jun 23, 2011). "Clinical practice. Chronic hepatitis C infection.". The New England Journal of Medicine 364 (25): 2429–38. doi:10.1056/NEJMcp1006613. PMID 21696309.
- "General Information About Adult Primary Liver Cancer". National Cancer Institute. Retrieved 13 January 2013.
- Jeong, SW; Jang, JY; Chung, RT (December 2012). "Hepatitis C virus and hepatocarcinogenesis.". Clinical and molecular hepatology 18 (4): 347–56. doi:10.3350/cmh.2012.18.4.347. PMID 23323249.
- Ralphs, S; Khan, SA (May 2013). "The role of the hepatitis viruses in cholangiocarcinoma.". Journal of viral hepatitis 20 (5): 297–305. doi:10.1111/jvh.12093. PMID 23565610.
- Kew, MC (March 2013). "Hepatitis viruses (other than hepatitis B and C viruses) as causes of hepatocellular carcinoma: an update.". Journal of viral hepatitis 20 (3): 149–57. doi:10.1111/jvh.12043. PMID 23383653.
- Fattovich, G; Stroffolini, T; Zagni, I; Donato, F (November 2004). "Hepatocellular carcinoma in cirrhosis: incidence and risk factors.". Gastroenterology 127 (5 Suppl 1): S35–50. doi:10.1053/j.gastro.2004.09.014. PMID 15508101.
- Kensler, TW; Roebuck, BD; Wogan, GN; Groopman, JD (March 2011). "Aflatoxin: a 50-year odyssey of mechanistic and translational toxicology". Toxicological sciences : an official journal of the Society of Toxicology. 120 Suppl 1: S28–48. doi:10.1093/toxsci/kfq283. PMC 3043084. PMID 20881231.
- Chuang, SC; La Vecchia, C; Boffetta, P (Dec 1, 2009). "Liver cancer: descriptive epidemiology and risk factors other than HBV and HCV infection". Cancer letters 286 (1): 9–14. doi:10.1016/j.canlet.2008.10.040. PMID 19091458.
- Di Tommaso, L; Sangiovanni, A; Borzio, M; Park, YN; Farinati, F; Roncalli, M (April 2013). "Advanced precancerous lesions in the liver.". Best practice & research. Clinical gastroenterology 27 (2): 269–84. doi:10.1016/j.bpg.2013.03.015. PMID 23809245.
- Razumilava, N; Gores, GJ (January 2013). "Classification, diagnosis, and management of cholangiocarcinoma.". Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 11 (1): 13–21.e1; quiz e3–4. doi:10.1016/j.cgh.2012.09.009. PMID 22982100.
- DeBaun, MR; Tucker, MA (March 1998). "Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry.". The Journal of pediatrics 132 (3 Pt 1): 398–400. doi:10.1016/S0022-3476(98)70008-3. PMID 9544889.
- Spector, LG; Birch, J (November 2012). "The epidemiology of hepatoblastoma.". Pediatric blood & cancer 59 (5): 776–9. doi:10.1002/pbc.24215. PMID 22692949.
- Davit-Spraul, A; Gonzales, E; Baussan, C; Jacquemin, E (Jan 8, 2009). "Progressive familial intrahepatic cholestasis". Orphanet journal of rare diseases 4: 1. doi:10.1186/1750-1172-4-1. PMC 2647530. PMID 19133130.
- Ariff, B; Lloyd, CR; Khan, S; Shariff, M; Thillainayagam, AV; Bansi, DS; Khan, SA; Taylor-Robinson, SD; Lim, AK (Mar 21, 2009). "Imaging of liver cancer". World journal of gastroenterology : WJG 15 (11): 1289–300. doi:10.3748/wjg.15.1289. PMC 2658841. PMID 19294758.
- Malaguarnera, G; Paladina, I; Giordano, M; Malaguarnera, M; Bertino, G; Berretta, M (2013). "Serum markers of intrahepatic cholangiocarcinoma". Disease markers 34 (4): 219–28. doi:10.3233/DMA-130964 (inactive 2014-11-10). PMID 23396291.
- Zhao, Y; Qiang, J; Li, C, Guan-Cheng; Ju, Q; Li, G. C. (2013). "Tumor markers for hepatocellular carcinoma (Review)". Molecular and Clinical Oncology 1 (4): 593–598. doi:10.3892/mco.2013.119. PMC 3915636. PMID 24649215.
- Hoshida, Y; Fuchs, BC; Tanabe, KK (Nov 1, 2012). "Prevention of hepatocellular carcinoma: potential targets, experimental models, and clinical challenges.". Current cancer drug targets 12 (9): 1129–59. doi:10.2174/156800912803987977. PMID 22873223.
- Bruix, J; Sherman, M; American Association for the Study of Liver, Diseases (March 2011). "Management of hepatocellular carcinoma: an update". Hepatology (Baltimore, Md.) 53 (3): 1020–2. doi:10.1002/hep.24199. PMID 21374666.
- Wang, ZG; Zhang, GF; Wu, JC; Jia, MK (August 2013). "Adjuvant therapy for hepatocellular carcinoma: Current situation and prospect.". Drug discoveries & therapeutics 7 (4): 137–143. doi:10.5582/ddt.2013.v7.4.137. PMID 24071575.
- de Lope, CR; Tremosini, S; Forner, A; Reig, M; Bruix, J (2012). "Management of HCC.". Journal of hepatology. 56 Suppl 1: S75–87. doi:10.1016/S0168-8278(12)60009-9. PMID 22300468.
- Feng, M; Ben-Josef, E (October 2011). "Radiation therapy for hepatocellular carcinoma.". Seminars in radiation oncology 21 (4): 271–7. doi:10.1016/j.semradonc.2011.05.002. PMID 21939856.
- Ulstrup, T; Pedersen, FM (Feb 25, 2013). "[Photodynamic therapy of cholangiocarcinomas].". Ugeskrift for laeger 175 (9): 579–82. PMID 23608009.
- Kuhlmann, JB; Blum, HE (May 2013). "Locoregional therapy for cholangiocarcinoma.". Current opinion in gastroenterology 29 (3): 324–8. doi:10.1097/MOG.0b013e32835d9dea. PMID 23337933.
- Ortner, MA (September 2011). "Photodynamic therapy for cholangiocarcinoma". Lasers in surgery and medicine 43 (7): 776–80. doi:10.1002/lsm.21106 (inactive 2014-11-10). PMID 22057505.
- Valero V, 3rd; Cosgrove, D; Herman, JM; Pawlik, TM (August 2012). "Management of perihilar cholangiocarcinoma in the era of multimodal therapy.". Expert review of gastroenterology & hepatology 6 (4): 481–95. doi:10.1586/egh.12.20. PMID 22928900.
- Meyers, RL; Czauderna, P; Otte, JB (November 2012). "Surgical treatment of hepatoblastoma.". Pediatric blood & cancer 59 (5): 800–8. doi:10.1002/pbc.24220. PMID 22887704.
- Perilongo, G; Malogolowkin, M; Feusner, J (November 2012). "Hepatoblastoma clinical research: lessons learned and future challenges.". Pediatric blood & cancer 59 (5): 818–21. doi:10.1002/pbc.24217. PMID 22678761.
- "WHO Disease and injury country estimates". World Health Organization. 2009. Retrieved Nov 11, 2009.
- Lozano, R; Naghavi, M; Foreman, K; Lim, S; Shibuya, K; Aboyans, V; Abraham, J; Adair, T; Aggarwal, R; Ahn, S. Y.; Alvarado, M; Anderson, H. R.; Anderson, L. M.; Andrews, K. G.; Atkinson, C; Baddour, L. M.; Barker-Collo, S; Bartels, D. H.; Bell, M. L.; Benjamin, E. J.; Bennett, D; Bhalla, K; Bikbov, B; Bin Abdulhak, A; Birbeck, G; Blyth, F; Bolliger, I; Boufous, S; Bucello, C et al. (Dec 15, 2012). "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010". Lancet 380 (9859): 2095–128. doi:10.1016/S0140-6736(12)61728-0. PMID 23245604.
- World Cancer Report 2014. International Agency for Research on Cancer, World Health Organization. 2014. ISBN 978-92-832-0432-9.
- El-Serag, HB; Rudolph, KL (June 2007). "Hepatocellular carcinoma: epidemiology and molecular carcinogenesis.". Gastroenterology 132 (7): 2557–76. doi:10.1053/j.gastro.2007.04.061. PMID 17570226.
- Khan, SA; Toledano, MB; Taylor-Robinson, SD (2008). "Epidemiology, risk factors, and pathogenesis of cholangiocarcinoma.". HPB : the official journal of the International Hepato Pancreato Biliary Association 10 (2): 77–82. doi:10.1080/13651820801992641. PMID 18773060.
- "Liver cancer statistics". Cancer Research UK. Retrieved 28 October 2014.
- "Liver cancer survival time tripled by virus". New Scientist. 10 February 2013. Retrieved 22 June 2013.
|Wikimedia Commons has media related to Liver cancer.|
- The Liver Cancer Web Page at Johns Hopkins University
- Liver cancer at Mayo Clinic
- Clinically reviewed liver cancer information