TY - JOUR
T1 - Influence of HIV infection on the natural history of hepatocellular carcinoma: Results from a global multicohort study
AU - Pinato, David J.
AU - Allara, Elias
AU - Chen, Ting Yi
AU - Trevisani, Franco
AU - Minguez, Beatriz
AU - Zoli, Marco
AU - Harris, Marianne
AU - Pria, Alessia Dalla
AU - Merchante, Nicolás
AU - Platt, Heather
AU - Jain, Mamta
AU - Caturelli, Eugenio
AU - Kikuchi, Luciana
AU - Pineda, Juan
AU - Nelson, Mark
AU - Farinati, Fabio
AU - Rapaccini, Gian Ludovico
AU - Aytaman, Ayse
AU - Yin, Michael
AU - Tan, Chee Kiat
AU - Bower, Mark
AU - Giannini, Edoardo G.
AU - Bräu, Norbert
PY - 2019/2/1
Y1 - 2019/2/1
N2 - © 2018 by American Society of Clinical Oncology. PURPOSE Conflicting evidence indicates that HIV seropositivity may influence the outcome of patients with hepatocellular carcinoma (HCC), a leading cause of mortality in people with HIV. We aimed to verify whether HIV affected the overall survival (OS) of patients with HCC, independent of treatment and geographic origin. PATIENTS AND METHODS We designed an international multicohort study of patients with HCC accrued from four continents who did not receive any anticancer treatment. We estimated the effect of HIV seropositivity on patients’ OS while accounting for common prognostic factors and demographic characteristics in uni- and multivariable models. RESULTS A total of 1,588 patients were recruited, 132 of whom were HIV positive. Most patients clustered within Barcelona Clinic Liver Cancer (BCLC) C or D criteria (n = 1,168 [74%]) and Child-Turcotte-Pugh (CTP) class B (median score, 7; interquartile range [IQR], 3). At HCC diagnosis, the majority of patients who were HIV-positive (n = 65 [64%]) had been on antiretrovirals for a median duration of 8.3 years (IQR, 8.59 years) and had median CD4 + cell counts of 256 (IQR, 284) with undetectable HIV RNA (n = 68 [52%]). OS decreased significantly throughout BCLC stages 0 to D (16, 12, 7.5, 3.1, and 3 months, respectively; P, .001). Median OS of patients who were HIV-positive was one half that of their HIV-uninfected counterparts (2.2 months [bootstrap 95% CI, 1.2 to 3.1 months] v 4.1 months [95% CI, 3.6 to 4.4 months]). In adjusted analyses, HIV seropositivity increased the hazard of death by 24% (P = .0333) independent of BCLC (P, .0001), CTP (P, .0001), a-fetoprotein (P, .0001), geographical origin (P, .0001), and male sex (P = .0016). Predictors of worse OS in patients who were HIV-positive included CTP (P = .0071) and a-fetoprotein (P, .0001). CONCLUSION Despite adequate antiretroviral treatment, HIV seropositivity is associated with decreased survival in HCC, independent of stage, anticancer treatment, and geographical origin. Mechanistic studies investigating the immunobiology of HIV-associated HCC are urgently required.
AB - © 2018 by American Society of Clinical Oncology. PURPOSE Conflicting evidence indicates that HIV seropositivity may influence the outcome of patients with hepatocellular carcinoma (HCC), a leading cause of mortality in people with HIV. We aimed to verify whether HIV affected the overall survival (OS) of patients with HCC, independent of treatment and geographic origin. PATIENTS AND METHODS We designed an international multicohort study of patients with HCC accrued from four continents who did not receive any anticancer treatment. We estimated the effect of HIV seropositivity on patients’ OS while accounting for common prognostic factors and demographic characteristics in uni- and multivariable models. RESULTS A total of 1,588 patients were recruited, 132 of whom were HIV positive. Most patients clustered within Barcelona Clinic Liver Cancer (BCLC) C or D criteria (n = 1,168 [74%]) and Child-Turcotte-Pugh (CTP) class B (median score, 7; interquartile range [IQR], 3). At HCC diagnosis, the majority of patients who were HIV-positive (n = 65 [64%]) had been on antiretrovirals for a median duration of 8.3 years (IQR, 8.59 years) and had median CD4 + cell counts of 256 (IQR, 284) with undetectable HIV RNA (n = 68 [52%]). OS decreased significantly throughout BCLC stages 0 to D (16, 12, 7.5, 3.1, and 3 months, respectively; P, .001). Median OS of patients who were HIV-positive was one half that of their HIV-uninfected counterparts (2.2 months [bootstrap 95% CI, 1.2 to 3.1 months] v 4.1 months [95% CI, 3.6 to 4.4 months]). In adjusted analyses, HIV seropositivity increased the hazard of death by 24% (P = .0333) independent of BCLC (P, .0001), CTP (P, .0001), a-fetoprotein (P, .0001), geographical origin (P, .0001), and male sex (P = .0016). Predictors of worse OS in patients who were HIV-positive included CTP (P = .0071) and a-fetoprotein (P, .0001). CONCLUSION Despite adequate antiretroviral treatment, HIV seropositivity is associated with decreased survival in HCC, independent of stage, anticancer treatment, and geographical origin. Mechanistic studies investigating the immunobiology of HIV-associated HCC are urgently required.
KW - Aged
KW - Anti-HIV Agents/therapeutic use
KW - Australia/epidemiology
KW - Carcinoma, Hepatocellular/diagnosis
KW - Europe/epidemiology
KW - Female
KW - HIV Infections/diagnosis
KW - HIV Seropositivity
KW - Humans
KW - Liver Neoplasms/diagnosis
KW - Male
KW - Middle Aged
KW - North America/epidemiology
KW - Prognosis
KW - Risk Assessment
KW - Risk Factors
KW - South America/epidemiology
KW - Time Factors
UR - http://www.mendeley.com/research/influence-hiv-infection-natural-history-hepatocellular-carcinoma-results-global-multicohort-study
U2 - 10.1200/JCO.18.00885
DO - 10.1200/JCO.18.00885
M3 - Article
C2 - 30562130
SN - 0732-183X
VL - 37
SP - 296
EP - 304
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
ER -