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ICAAC 2013: Liver Cancer Often Diagnosed Late with Poor Survival in People with HIV

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Hepatocellular carcinoma (HCC) is frequently diagnosed at an advanced stage in HIV positive people with hepatitis B or C coinfection, contributing to a high mortality rate that has changed little in recent years, according to a report at the recent 53rd Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC 2013) in Denver.

Over years or decades chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection can lead to severe liver disease including cirrhosis and hepatocellular carcinoma, a type of primary liver cancer.

People coinfected with HIV and viral hepatitis tend to experience more rapid liver disease progression and respond less well to treatment than those with HBV or HCV alone. As antiretroviral therapy has reduced mortality due to AIDS, liver disease including HCC has become a growing cause of death among people with HIV.

Juan Berenguer from Hospital General Universitario Gregorio Marañón in Madrid presented findings from an analysis of tumor characteristics and survival among HIV positive patients with HCC. The researchers looked at how these have been affected by surveillance practices, comparing outcomes before and after publication of the American Association for the Study of the Liver (AASLD) HCC practice guideline in 2005.

Guidelines recommend that people at risk for HCC should undergo screening every 6 months. Risk factors include older age, active HBV replication or inflammatory activity, HCV infection, non-alcoholic steatosis (fatty liver), and liver cirrhosis due to any cause. Although most people develop HCC after they already have advanced fibrosis or cirrhosis, it sometimes also occurs in people with less advanced liver disease. Screening should include ultrasound imaging to detect tumors and may also include liver biopsies and measurement of alpha fetoprotein (AFP), a blood biomarker linked to HCC and other types of cancer.

Berenguer's group did a retrospective analysis of medical records from all HIV positive patients diagnosed with HCC at their center between October 1998 and April 2012. Surveillance was defined as having undergone liver imaging within the 12 months prior to HCC diagnosis. HCC was diagnosed using non-invasive methods or pathology and staged using the Barcelona Clinic Liver Cancer (BCLC) classification system:

  • 0: Very early -- single tumor <2 cm or carcinoma in situ with Child-Pugh score of A and ECOG performance status of 0;
  • A: Early -- single tumor <5 cm or 3 nodules <3 cm with Child-Pugh A or B and ECOG of 0;
  • B: Intermediate -- single tumor >5 cm or multinodular with Child-Pugh A or B and ECOG of 0;
  • C: Advanced -- portal invasion, nodes, or metastasis with Child-Pugh A or B and ECOG of 1-2;
  • D: End-stage -- any tumor pattern with Child-Pugh score of C and ECOG of 3-4.

Attempts at curative therapy such as resection (tumor removal) are generally recommended for BCLC stages 0 or A, palliative therapy for stages B or C, and management of symptoms only for stage D.

The researchers identified 53 HIV positive patients with HCC during the study period; 19 were diagnosed during 1998-2005 and 34 during 2006-2012. All but 6 (89%) were men and 82% had a history of injection drug use.

Most (87%) were on combination antiretroviral therapy. Patients diagnosed with HCC during 1998-2005 were younger (44 vs 48 years), had a higher MELD score (12 vs 10), and were more likely to have undetectable HIV viral load (47% vs 79%) than those diagnosed during 2006-2012. The median CD4 T-cell count was also lower (272 vs 357 cells/mm3), but not significantly so.

Results

  • Looking at liver disease characteristics, all patients diagnosed with HCC had HCV (77%), HBV (11%), or both (11%).
  • Almost all (95%) had cirrhosis, 60% had a Child-Pugh score of B or C, and half experienced liver decompensation.
  • More people were treated for hepatitis C with pegylated interferon/ribavirin during the second period (32% vs 47%), but the difference did not reach statistical significance; Berenguer noted that none of the treated patients achieved sustained virological response, or a cure.
  • Fewer than half of participants had HCC diagnosed through surveillance during either period (42% during 1998-2005 and 41% during 2006-2012), indicating no change after the AASLD guidelines were issued; biopsy confirmation, however, was more common during the first period (37% vs 15%).
  • People diagnosed during the first period were less likely to have single tumors (32% vs 41%), more likely to have large tumors >5 cm (67% vs 44%), had more metastases (21% vs 12%), and were more likely to have BCLC stages C or D (68% vs 47%), but none of these differences reached statistical significance.
  • People diagnosed during 1998-2005 were significantly less likely to receive treatment for HCC than those diagnosed later (42% vs 71%).
  • This included potentially curative therapies such as radiofrequency or ethanol ablation (8% vs 22%) and resection (2% vs 6%), as well as palliative therapies such as transarterial chemoembolization (11% vs 17%) and sorafenib (2% vs 9%); patients in the latter period were more than twice as likely to undergo multiple types of treatment (11% vs 24%).
  • Consistent with having less advanced disease characteristics and receiving more treatment, survival was longer during the second period compared with the first (median 2 vs 11 months).
  • Proportions of people surviving were higher during the second period for 1-year survival (37% vs 62%), 2-year survival (26% vs 37%), and 3-year survival (14% vs 28%), but none of these differences reached statistical significance, meaning they could be attributable to chance (P=0.16).
  • In a univariate analysis, factors significantly associated with higher mortality included detectable HIV viral load, higher MELD score, BCLC stage C-D vs A-B, and AFP level >200 ng/dL.
  • Receiving any type of treatment was associated with a significant 75% lower risk of death.
  • CD4 cell count, Child-Pugh score, alcohol consumption, and HCC screening had no significant impact.

"In people with HIV, HCC was frequently diagnosed at an advanced stage and outside of surveillance programs," the researchers concluded. "Mortality was very high, with no significant changes in recent years."

Berenguer stated that "probably all patients with cirrhosis" are at risk of developing liver cancer, and further studies are needed to see if some people are especially at risk. He recommended screening HIV-positive people with advanced liver disease at least every 6 months.

10/1/13

Reference

A Díaz-Sánchez, P Miralles, A Matilla, J Berenguer, et al. Tumor characteristics and survival in HIV-infected patients with hepatocellular carcinoma: the impact of surveillance‚Ä®. 53rd Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC 2013). Denver, September 10-13, 2013.Abstract H-1529.