TY - JOUR
T1 - Cachexia is Prevalent in Patients With Hepatocellular Carcinoma and Associated With Worse Prognosis
AU - Rich, Nicole E.
AU - Phen, Samuel
AU - Desai, Nirali
AU - Mittal, Sukul
AU - Yopp, Adam C.
AU - Yang, Ju Dong
AU - Marrero, Jorge A
AU - Iyengar, Puneeth
AU - Infante, Rodney E.
AU - Singal, Amit G.
N1 - Funding Information:
Conflicts of interest These authors disclose the following: Nicole Rich serves as a consultant for AstraZeneca. Jorge Marrero has served as a consultant for Glycotest and received research funding from AstraZeneca. Amit Singal has been on advisory boards and served as a consultant for Wako Diagnostics, Roche, Exact Sciences, Glycotest, GRAIL, Bayer, Eisai, Exelixis, BMS, AstraZeneca, Genentech, and TARGET-RWE. Pfizer, Inc. is currently supporting a collaborative project with the laboratory of Rodney Infante that is independent of all data presented in this manuscript. The remaining authors disclose no conflicts.
Funding Information:
Nicole E. Rich (Conceptualization: Equal; Data curation: Lead; Formal analysis: Equal; Methodology: Equal; Visualization: Lead; Writing – original draft: Lead; Writing – review & editing: Equal), Samuel Phen (Data curation: Equal; Writing – review & editing: Supporting; data abstraction: Equal), Nirali Desai (Data curation: Equal; Writing – review & editing: Supporting; data abstraction: Equal), Sukul Mittal (Data curation: Equal; Writing – review & editing: Supporting; data abstraction: Supporting), Adam C. Yopp (Writing – review & editing: Supporting), Ju Dong Yang (Visualization: Supporting; Writing – review & editing: Supporting), Jorge A. Marrero (Visualization: Equal; Writing – review & editing: Supporting), Puneeth Iyengar (Formal analysis: Supporting; Writing – review & editing: Supporting), Rodney E. Infante (Conceptualization: Equal; Formal analysis: Supporting; Writing – review & editing: Supporting), Amit G. Singal (Conceptualization: Equal; Data curation: Supporting; Formal analysis: Supporting; Funding acquisition: Lead; Methodology: Equal; Project administration: Lead; Resources: Lead; Software: Lead; Supervision: Lead; Visualization: Equal; Writing – original draft: Supporting; Writing – review & editing: Equal)
Funding Information:
Funding Amit G. Singal is supported by National Institutes of Health grants R01 CA222900 and R01 MD12565. Jorge A. Marrero is supported by National Institutes of Health grant R01 CA237659. Rodney E. Infante is supported by Burroughs Wellcome Fund Career Awards for Medical Scientists (1019692); American Gastroenterological Association Scholar Award (2019AGARSA3); American Cancer Society grant (133889-RSG-19-195-01-TBE); Cancer Prevention and Research Institute of Texas (RP200170); and the V Foundation Scholar Award (V2019-014). Nicole E. Rich is supported by the American College of Gastroenterology Junior Faculty Development Award and the Texas Health Resources Clinical Scholar Award. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2022 AGA Institute
PY - 2022/5
Y1 - 2022/5
N2 - Background & Aims: Cancer cachexia is a wasting syndrome associated with functional impairment and reduced survival that impacts up to 50% of patients with gastrointestinal cancers. However, data are limited on the prevalence and clinical significance of cachexia in patients with hepatocellular carcinoma (HCC). Methods: We performed a retrospective cohort study of patients diagnosed with HCC at 2 United States health systems between 2008 and 2018. Patient weights were recorded 6 months prior to and at time of HCC diagnosis. Cachexia was defined as >5% weight loss (or >2% weight loss if body mass index <20 kg/m2), and precachexia was defined as 2% to 5% weight loss. We used multivariable logistic regression models to identify correlates of cachexia and multivariable Cox proportional hazard models to identify factors associated with overall survival. Results: Of 604 patients with HCC, 201 (33.3%) had precachexia and 143 (23.7%) had cachexia at diagnosis, including 19.0%, 23.5%, 34.7%, and 34.0% of patients with Barcelona Clinic Liver Cancer stages 0/A, B, C, and D, respectively. Patients with cachexia were less likely to receive HCC treatment (odds ratio, 0.38; 95% confidence interval, 0.21–0.71) and had worse survival than those with precachexia or stable weight (11.3 vs 20.4 vs 23.5 months, respectively; P <.001). Cachexia remained independently associated with worse survival (hazard ratio, 1.43; 95% confidence interval, 1.11–1.84) after adjusting for age, sex, race, ethnicity, Child Pugh class, alpha-fetoprotein, Barcelona Clinic Liver Cancer stage, and HCC treatment. Conclusions: Nearly 1 in 4 patients with HCC present with cachexia, including many with compensated cirrhosis or early stage tumors. The presence of cancer-associated weight loss appears to be an early and independent predictor of worse outcomes in patients with HCC.
AB - Background & Aims: Cancer cachexia is a wasting syndrome associated with functional impairment and reduced survival that impacts up to 50% of patients with gastrointestinal cancers. However, data are limited on the prevalence and clinical significance of cachexia in patients with hepatocellular carcinoma (HCC). Methods: We performed a retrospective cohort study of patients diagnosed with HCC at 2 United States health systems between 2008 and 2018. Patient weights were recorded 6 months prior to and at time of HCC diagnosis. Cachexia was defined as >5% weight loss (or >2% weight loss if body mass index <20 kg/m2), and precachexia was defined as 2% to 5% weight loss. We used multivariable logistic regression models to identify correlates of cachexia and multivariable Cox proportional hazard models to identify factors associated with overall survival. Results: Of 604 patients with HCC, 201 (33.3%) had precachexia and 143 (23.7%) had cachexia at diagnosis, including 19.0%, 23.5%, 34.7%, and 34.0% of patients with Barcelona Clinic Liver Cancer stages 0/A, B, C, and D, respectively. Patients with cachexia were less likely to receive HCC treatment (odds ratio, 0.38; 95% confidence interval, 0.21–0.71) and had worse survival than those with precachexia or stable weight (11.3 vs 20.4 vs 23.5 months, respectively; P <.001). Cachexia remained independently associated with worse survival (hazard ratio, 1.43; 95% confidence interval, 1.11–1.84) after adjusting for age, sex, race, ethnicity, Child Pugh class, alpha-fetoprotein, Barcelona Clinic Liver Cancer stage, and HCC treatment. Conclusions: Nearly 1 in 4 patients with HCC present with cachexia, including many with compensated cirrhosis or early stage tumors. The presence of cancer-associated weight loss appears to be an early and independent predictor of worse outcomes in patients with HCC.
KW - Body Mass Index
KW - Cachexia
KW - Liver Cancer
KW - Wasting
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U2 - 10.1016/j.cgh.2021.09.022
DO - 10.1016/j.cgh.2021.09.022
M3 - Article
C2 - 34555519
AN - SCOPUS:85124143272
SN - 1542-3565
VL - 20
SP - e1157-e1169
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 5
ER -