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Liver cancer: Difference between revisions
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(Created page with "Hepatocellular carcinoma (<abbr>HCC</abbr>) is the most common primary malignant tumor of the liver. It’s mostly a disease of older men. In almost all cases it develops in an already cirrhotic liver, so the risk factors for HCC are the same as those for cirrhosis. The incidence of HCC is increasing. Due to the long asymptomatic period, most cases are irresectable at presentation. This gives it a poor prognosis, with a 5-year survival of 30 – 50%. == Etiology == Com...") |
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Hepatocellular carcinoma (<abbr>HCC</abbr>) is the most common primary malignant tumor of the liver. It’s mostly a disease of older men. In almost all cases it develops in an already cirrhotic liver, so the risk factors for HCC are the same as those for cirrhosis. | '''Hepatocellular carcinoma''' (<abbr>HCC</abbr>) is the most common primary malignant tumor of the liver. It’s mostly a disease of older men. In almost all cases it develops in an already [[Cirrhosis|cirrhotic]] liver, so the risk factors for HCC are the same as those for cirrhosis. | ||
The incidence of HCC is increasing. Due to the long asymptomatic period, most cases are irresectable at presentation. This gives it a poor prognosis, with a 5-year survival of 30 – 50%. | The incidence of HCC is increasing. Due to the long asymptomatic period, most cases are irresectable at presentation. This gives it a poor prognosis, with a 5-year survival of 30 – 50%. | ||
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Common causes: | Common causes: | ||
* Chronic HBV or HCV infection | * Chronic [[Hepatitis B|HBV]] or [[Hepatitis C|HCV]] infection | ||
* | * [[Metabolic associated fatty liver disease]] | ||
* Alcoholic liver disease | * [[Alcoholic liver disease]] | ||
* Aflatoxin | * [[Aflatoxin]] (rare outside the developing world) | ||
Rare causes: | Rare causes: | ||
* Hepatotoxic drugs like paracetamol | * Hepatotoxic drugs like [[paracetamol]] | ||
* Haemochromatosis | * [[Haemochromatosis]] | ||
* Autoimmune hepatitis | * [[Autoimmune hepatitis]] | ||
* Alpha-1-antitrypsin deficiency | * [[Alpha-1-antitrypsin deficiency]] | ||
* | * [[Wilson disease]] | ||
* Hepatic adenoma | * [[Benign liver tumours and tumour-like lesions|Hepatic adenoma]] | ||
== Pathology == | == Pathology == | ||
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Hepatitis B may incorporate the HBsAg into the host genome. Hepatitis C has no such capacity. Both viruses increase cancer risk due to the chronic inflammation and high cell turnover they cause. | Hepatitis B may incorporate the HBsAg into the host genome. Hepatitis C has no such capacity. Both viruses increase cancer risk due to the chronic inflammation and high cell turnover they cause. | ||
Aflatoxin causes a very characteristic mutation in the p53 gene called a signature mutation. If this mutation is present in an HCC it’s certain that the etiology was aflatoxin | Aflatoxin causes a very characteristic mutation in the p53 gene called a signature mutation. If this mutation is present in an HCC it’s certain that the etiology was aflatoxin. | ||
A special form of HCC called ''fibrolamellar HCC'' is very rare. Only 200 new cases are diagnosed every year. This type of HCC develops in young adults without cirrhosis or other risk factors for HCC. | A special form of HCC called ''fibrolamellar HCC'' is very rare. Only 200 new cases are diagnosed every year. This type of HCC develops in young adults without cirrhosis or other risk factors for HCC. | ||
== Clinical features == | == Clinical features == | ||
The tumour itself is usually asymptomatic, but the patient usually has symptoms from the underlying disease (cirrhosis or hepatitis). Constitutional cancer symptoms like weight loss, weakness, abdominal pain may be present but may also be caused by the underlying disease | The tumour itself is usually asymptomatic, but the patient usually has symptoms from the underlying disease ([[cirrhosis]] or [[hepatitis]]), like [[ascites]] and [[jaundice]]. [[Constitutional cancer symptom|Constitutional cancer symptoms]] like weight loss, weakness, abdominal pain may be present but may also be caused by the underlying disease. | ||
== Diagnosis and evaluation == | == Diagnosis and evaluation == | ||
Patients at high risk for <abbr>HCC</abbr> (cirrhosis of any cause, chronic hep B) should be screened regularly for HCC. Screening involves measuring abdominal ultrasound and AFP levels. Focal lesions in a cirrhotic liver are primary liver cancer until proven otherwise. AFP is elevated only in 50% of cases, in which case the level correlates with the tumour size. | Patients at high risk for <abbr>HCC</abbr> (cirrhosis of any cause, chronic hep B) should be screened regularly for HCC. Screening involves measuring abdominal [[ultrasound]] and [[AFP]] levels. Focal lesions in a cirrhotic liver are primary liver cancer until proven otherwise. AFP is elevated only in 50% of cases, in which case the level correlates with the tumour size. | ||
Contrast CT or MR confirms the diagnosis and shows extrahepatic spread. Typical features on imaging include early contrast uptake, “washout”, and vascular spread. | Contrast [[CT]] or [[MR]] confirms the diagnosis and shows extrahepatic spread. Typical features on imaging include early contrast uptake, “washout”, and vascular spread. | ||
Liver biopsy is often not needed as the definitive diagnosis can be made with imaging, and biopsy carries a risk of bleeding and tumour spread. | [[Liver biopsy]] is often not needed as the definitive diagnosis can be made with imaging, and biopsy carries a risk of bleeding and tumour spread. | ||
== Staging == | == Staging == | ||
The Barcelona Clinic Liver Cancer (BCLC) staging is the most frequently used staging system, and at least the one preferred in POTE. The Child-Pugh score and ECOG are important in determining the BCLC stage. | The Barcelona Clinic Liver Cancer (BCLC) staging is the most frequently used staging system, and at least the one preferred in POTE. The Child-Pugh score and ECOG are important in determining the BCLC stage. | ||
The Child-Pugh score involves multiple parameters that reflect liver function (bilirubin, albumin, PTT, INR, etc.) and classifies the function as Child-Pugh A, B, or C, where A is good liver function and C is poor liver function. | The [[Child-Pugh score]] involves multiple parameters that reflect liver function (bilirubin, albumin, PTT, INR, etc.) and classifies the function as Child-Pugh A, B, or C, where A is good liver function and C is poor liver function. | ||
The BCLC staging determines which stage the disease is in, based on the TNM staging, ECOG, and Child-Pugh score: | The BCLC staging determines which stage the disease is in, based on the TNM staging, ECOG, and Child-Pugh score: | ||
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*** Sectionectomy | *** Sectionectomy | ||
** Atypical resection | ** Atypical resection | ||
* Liver transplantation | * [[Liver transplantation]] | ||
* Local ablation | * Local [[ablation]] | ||
** Radiofrequency or microwave ablation | ** Radiofrequency or microwave ablation | ||
** Percutaneous ethanol injection | ** Percutaneous ethanol injection | ||
* Oncotherapy[[File:Treatment of HCC.gif|thumb|Treatment of HCC. From <nowiki>https://abdominalkey.com/liver-transplantation-for-hcc-the-milan-criteria/</nowiki>]] | * Oncotherapy[[File:Treatment of HCC.gif|thumb|Treatment of HCC. From <nowiki>https://abdominalkey.com/liver-transplantation-for-hcc-the-milan-criteria/</nowiki>]] | ||
** TACE (transarterial chemo-embolisation) | ** TACE (transarterial chemo-embolisation) | ||
** Targeted drug therapy (sorafenib) | ** Targeted drug therapy ([[sorafenib]]) | ||
The choice of modality depends on the BCLC stage. | The choice of modality depends on the BCLC stage. | ||