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Provider Attitudes and Practice Patterns for Direct-Acting Antiviral Therapy for Patients With Hepatocellular Carcinoma.
Rich, Nicole E; Yang, Ju Dong; Perumalswami, Ponni V; Alkhouri, Naim; Jackson, Whitney; Parikh, Neehar D; Mehta, Neil; Salgia, Reena; Duarte-Rojo, Andres; Kulik, Laura; Rakoski, Mina; Said, Adnan; Oloruntoba, Omobonike; Ioannou, George N; Hoteit, Maarouf A; Moon, Andrew M; Rangnekar, Amol S; Eswaran, Sheila L; Zheng, Elizabeth; Jou, Janice H; Hanje, James; Pillai, Anjana; Hernaez, Ruben; Wong, Robert; Scaglione, Steven; Samant, Hrishikesh; Kapuria, Devika; Chandna, Shaun; Rosenblatt, Russell; Ajmera, Veeral; Frenette, Catherine T; Satapathy, Sanjaya K; Mantry, Parvez; Jalal, Prasun; John, Binu V; Fix, Oren K; Leise, Michael; Lindenmeyer, Christina C; Flores, Avegail; Patel, Nayan; Jiang, Z Gordon; Latt, Nyan; Dhanasekaran, Renumathy; Odewole, Mobolaji; Kagan, Sofia; Marrero, Jorge A; Singal, Amit G.
Afiliación
  • Rich NE; Division of Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas. Electronic address: nicole.rich@utsouthwestern.edu.
  • Yang JD; Division of Digestive and Liver Diseases, Comprehensive Transplant Center and Samuel Oschin Comprehensive Cancer Institute, Cedars Sinai Medical Center, Los Angeles, California.
  • Perumalswami PV; Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Alkhouri N; Texas Liver Institute, University of Texas Health San Antonio, San Antonio, Texas.
  • Jackson W; Division of Gastroenterology and Hepatology, University of Colorado Denver School of Medicine, Denver, Colorado.
  • Parikh ND; Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan.
  • Mehta N; Division of Gastroenterology, University of California San Francisco, San Francisco, California.
  • Salgia R; Division of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, Michigan.
  • Duarte-Rojo A; T.E. Starzl Transplantation Institute and Center for Liver Disease, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
  • Kulik L; Division of Hepatology, Northwestern University, Chicago, Illinois.
  • Rakoski M; Transplantation Institute and Division of Gastroenterology, Loma Linda University Health, Loma Linda, California.
  • Said A; Division of Gastroenterology and Hepatology, University of Wisconsin School of Medicine, Madison, Wisconsin.
  • Oloruntoba O; Division of Gastroenterology and Hepatology, Duke University Health Center, Durham, North Carolina.
  • Ioannou GN; Division of Gastroenterology and Research and Development, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, Washington.
  • Hoteit MA; Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Moon AM; Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, North Carolina.
  • Rangnekar AS; Division of Gastroenterology, Georgetown University Hospital, Washington, DC.
  • Eswaran SL; Division of Gastroenterology, Rush Medical College, Chicago, Illinois.
  • Zheng E; Division of Digestive and Liver Diseases, Columbia University, New York, New York.
  • Jou JH; Division of Gastroenterology and Hepatology, Oregon Health and Science University, Portland, Oregon.
  • Hanje J; Division of Gastroenterology, Hepatology and Nutrition, The Ohio State University Wexner Medical Center, Columbus, Ohio.
  • Pillai A; Division of Gastroenterology, Hepatology and Nutrition, University of Chicago, Chicago, Illinois.
  • Hernaez R; Section of Gastroenterology and Hepatology, Baylor College of Medicine and Michael E. Debakey Veterans Affairs Medical Center, Houston, Texas.
  • Wong R; Division of Gastroenterology and Hepatology, Alameda Health System, Oakland, California.
  • Scaglione S; Division of Hepatology, Loyola University Medical Center and Edward Hines Veterans Affairs, Chicago, Illinois.
  • Samant H; Division of Gastroenterology and Hepatology, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
  • Kapuria D; Division of Gastroenterology and Hepatology, University of New Mexico, Albuquerque, New Mexico.
  • Chandna S; Division of Gastroenterology, Hepatology and Nutrition, University of Utah, Salt Lake City, Utah.
  • Rosenblatt R; Division of Gastroenterology and Hepatology, Weill Cornell Medicine - New York-Presbyterian Hospital, New York, New York.
  • Ajmera V; Division of Gastroenterology and Hepatology, University of California San Diego, San Diego, California.
  • Frenette CT; Division of Organ Transplantation, Scripps Green Hospital, San Diego, California.
  • Satapathy SK; Division of Transplant Surgery, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Mantry P; Liver Institute at Methodist Dallas, Dallas, Texas.
  • Jalal P; Division of Abdominal Transplantation, Baylor College of Medicine, Houston, Texas.
  • John BV; Division of Gastroenterology and Hepatology, McGuire Veterans Affairs Medical Center, Richmond, Virginia.
  • Fix OK; Organ Transplant Department, Swedish Medical Center, Seattle, Washington.
  • Leise M; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Lindenmeyer CC; Digestive Disease & Surgery Institute, Cleveland Clinic, Cleveland, Ohio.
  • Flores A; Division of Gastroenterology, Washington University School of Medicine, St. Louis, Missouri.
  • Patel N; Banner Transplant Institute, Banner - University Medical Center Phoenix, Phoenix, Arizona.
  • Jiang ZG; Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Latt N; Oschner Multi-Organ Transplant Institute, Oschner Health System, New Orleans, Louisiana.
  • Dhanasekaran R; Division of Gastroenterology and Hepatology, Stanford University, Stanford, California.
  • Odewole M; Division of Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas.
  • Kagan S; Division of Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas.
  • Marrero JA; Division of Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas.
  • Singal AG; Division of Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas.
Clin Gastroenterol Hepatol ; 18(4): 974-983, 2020 04.
Article en En | MEDLINE | ID: mdl-31357028
BACKGROUND & AIMS: Direct-acting antivirals (DAAs) are effective against hepatitis C virus and sustained virologic response is associated with reduced incidence of hepatocellular carcinoma (HCC). However, there is controversy over the use of DAAs in patients with active or treated HCC and uncertainty about optimal management of these patients. We aimed to characterize attitudes and practice patterns of hepatology practitioners in the United States regarding the use of DAAs in patients with HCC. METHODS: We conducted a survey of hepatology providers at 47 tertiary care centers in 25 states. Surveys were sent to 476 providers and we received 279 responses (58.6%). RESULTS: Provider beliefs about risk of HCC recurrence after DAA therapy varied: 48% responded that DAAs reduce risk, 36% responded that DAAs do not change risk, and 16% responded that DAAs increase risk of HCC recurrence. However, most providers believed DAAs to be beneficial to and reduce mortality of patients with complete response to HCC treatment. Accordingly, nearly all providers (94.9%) reported recommending DAA therapy to patients with early-stage HCC who received curative treatment. However, fewer providers recommended DAA therapy for patients with intermediate (72.9%) or advanced (57.5%) HCC undergoing palliative therapies. Timing of DAA initiation varied among providers based on HCC treatment modality: 49.1% of providers reported they would initiate DAA therapy within 3 months of surgical resection whereas 45.9% and 5.0% would delay DAA initiation for 3-12 months and >1 year post-surgery, respectively. For patients undergoing transarterial chemoembolization (TACE), 42.0% of providers would provide DAAs within 3 months of the procedure, 46.7% would delay DAAs until 3-12 months afterward, and 11.3% would delay DAAs more than 1 year after TACE. CONCLUSIONS: Based on a survey sent to hepatology providers, there is variation in provider attitudes and practice patterns regarding use and timing of DAAs for patients with HCC. Further studies are needed to characterize the risks and benefits of DAA therapy in this patient population.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Quimioembolización Terapéutica / Carcinoma Hepatocelular / Hepatitis C Crónica / Neoplasias Hepáticas Límite: Humans Idioma: En Revista: Clin Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Quimioembolización Terapéutica / Carcinoma Hepatocelular / Hepatitis C Crónica / Neoplasias Hepáticas Límite: Humans Idioma: En Revista: Clin Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos