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Hepatocellular Carcinoma Demonstrates Heterogeneous Growth Patterns in a Multicenter Cohort of Patients With Cirrhosis.
Rich, Nicole E; John, Binu V; Parikh, Neehar D; Rowe, Ian; Mehta, Neil; Khatri, Gaurav; Thomas, Smitha M; Anis, Munazza; Mendiratta-Lala, Mishal; Hernandez, Christopher; Odewole, Mobolaji; Sundaram, Latha T; Konjeti, Venkata R; Shetty, Shishir; Shah, Tahir; Zhu, Hao; Yopp, Adam C; Hoshida, Yujin; Yao, Francis Y; Marrero, Jorge A; Singal, Amit G.
Afiliación
  • Rich NE; Division of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • John BV; Division of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, VA.
  • Parikh ND; Division of Gastroenterology and Hepatology, Virginia Commonwealth University, Richmond, VA.
  • Rowe I; Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, MI.
  • Mehta N; Leeds Institute for Data Analytics, University of Leeds, Leeds, United Kingdom.
  • Khatri G; Leeds Liver Unit, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
  • Thomas SM; Division of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, CA.
  • Anis M; Department of Radiology, University of Texas Southwestern Medical Center, Dallas, TX.
  • Mendiratta-Lala M; Department of Radiology, McGuire VA Medical Center, Richmond, VA.
  • Hernandez C; Department of Radiology, McGuire VA Medical Center, Richmond, VA.
  • Odewole M; Department of Radiology, University of Michigan, Ann Arbor, MI.
  • Sundaram LT; Division of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • Konjeti VR; Division of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • Shetty S; Division of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, VA.
  • Shah T; Division of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, VA.
  • Zhu H; Centre for Liver Research, University of Birmingham and Liver and Hepatobiliary Unit, Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom.
  • Yopp AC; Liver and Hepatobiliary Unit, Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom.
  • Hoshida Y; Children's Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.
  • Yao FY; Department of Surgery, University of Texas Southwestern Medical Center, Dallas, TX.
  • Marrero JA; Division of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • Singal AG; Division of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, CA.
Hepatology ; 72(5): 1654-1665, 2020 11.
Article en En | MEDLINE | ID: mdl-32017165
ABSTRACT
BACKGROUND AND

AIMS:

There are limited data on hepatocellular carcinoma (HCC) growth patterns, particularly in Western cohorts, despite implications for surveillance, prognosis, and treatment. Our study's aim was to quantify tumor doubling time (TDT) and identify correlates associated with indolent and rapid growth. APPROACH AND

RESULTS:

We performed a retrospective multicenter cohort study of patients with cirrhosis diagnosed with HCC from 2008 to 2017 at six US and European health systems with two or more contrast-enhanced imaging studies performed ≥ 30 days apart prior to HCC treatment. Radiologists independently measured tumors in three dimensions to calculate TDT and specific growth rate (SGR). We used multivariable ordinal logistic regression to identify factors associated with indolent (TDT > 365 days) and rapid (TDT < 90 days) tumor growth. In the primary cohort (n = 242 patients from four centers), median TDT was 229 days (interquartile range [IQR], 89-627) and median SGR was 0.3% per day (IQR, 0.1%-0.8%). Over one-third (38%) of HCCs had indolent growth, 36.8% intermediate growth, and 25.2% rapid growth. In multivariable analysis, indolent growth was associated with larger tumor diameter (odds ratio [OR], 1.15, 95% confidence interval [CI], 1.03-1.30) and alpha-fetoprotein < 20 ng/mL (OR, 1.90; 95% CI, 1.12-3.21). Indolent growth was more common in nonviral than viral cirrhosis (50.9% versus 32.1%), particularly in patients with T1 HCC (OR, 3.41; 95% CI, 1.08-10.80). Median TDT (169 days; IQR 74-408 days) and SGR (0.4% per day) were similar in an independent cohort (n = 176 patients from two centers).

CONCLUSIONS:

In a large Western cohort of patients with HCC, we found heterogeneous tumor growth patterns, with one-fourth exhibiting rapid growth and over one-third having indolent growth. Better understanding different tumor growth patterns may facilitate a precision approach to prognostication and treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Cirrosis Hepática / Neoplasias Hepáticas Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatology Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Cirrosis Hepática / Neoplasias Hepáticas Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatology Año: 2020 Tipo del documento: Article