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International, evidence-based consensus treatment guidelines for idiopathic multicentric Castleman disease.
van Rhee, Frits; Voorhees, Peter; Dispenzieri, Angela; Fosså, Alexander; Srkalovic, Gordan; Ide, Makoto; Munshi, Nikhil; Schey, Stephen; Streetly, Matthew; Pierson, Sheila K; Partridge, Helen L; Mukherjee, Sudipto; Shilling, Dustin; Stone, Katie; Greenway, Amy; Ruth, Jason; Lechowicz, Mary Jo; Chandrakasan, Shanmuganathan; Jayanthan, Raj; Jaffe, Elaine S; Leitch, Heather; Pemmaraju, Naveen; Chadburn, Amy; Lim, Megan S; Elenitoba-Johnson, Kojo S; Krymskaya, Vera; Goodman, Aaron; Hoffmann, Christian; Zinzani, Pier Luigi; Ferrero, Simone; Terriou, Louis; Sato, Yasuharu; Simpson, David; Wong, Raymond; Rossi, Jean-Francois; Nasta, Sunita; Yoshizaki, Kazuyuki; Kurzrock, Razelle; Uldrick, Thomas S; Casper, Corey; Oksenhendler, Eric; Fajgenbaum, David C.
Afiliação
  • van Rhee F; Myeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR.
  • Voorhees P; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, NC.
  • Dispenzieri A; Division of Hematology/Oncology, Mayo Clinic, Rochester, MN.
  • Fosså A; Department of Oncology, Oslo University Hospital-Norwegian Radium Hospital, Oslo, Norway.
  • Srkalovic G; Herbert-Herman Cancer Center, Michigan State University College of Human Medicine, Lansing, MI.
  • Ide M; Department of Hematology, Takamatsu Red Cross Hospital, Takamatsu, Kagawa, Japan.
  • Munshi N; Dana-Farber Cancer Institute, VA Boston Healthcare System, Harvard Medical School, Boston, MA.
  • Schey S; Guys and St. Thomas' NHS Foundation Trust, London, United Kingdom.
  • Streetly M; Guys and St. Thomas' NHS Foundation Trust, London, United Kingdom.
  • Pierson SK; Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Partridge HL; Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Mukherjee S; Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
  • Shilling D; Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Stone K; Myeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR.
  • Greenway A; Myeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR.
  • Ruth J; Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
  • Lechowicz MJ; Department of Hematology and Medical Oncology, and.
  • Chandrakasan S; Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University, Atlanta, GA.
  • Jayanthan R; Department of Medicine, Baylor College of Medicine, Houston, TX.
  • Jaffe ES; National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Leitch H; Division of Hematology, Department of Medicine, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Pemmaraju N; Division of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Chadburn A; Department of Pathology, Weill Cornell Medical College, New York, NY.
  • Lim MS; Department of Pathology and Laboratory Medicine, and.
  • Elenitoba-Johnson KS; Department of Pathology and Laboratory Medicine, and.
  • Krymskaya V; Penn Center for Pulmonary Biology, Pulmonary, Allergy, and Critical Care Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Goodman A; Division of Hematology/Oncology, Department of Medicine, University of California San Diego, La Jolla, CA.
  • Hoffmann C; University of Schleswig Holstein, Campus Kiel, Kiel, Germany.
  • Zinzani PL; ICH Study Center, Hamburg, Germany.
  • Ferrero S; Institute of Hematology "L. e A. Seràgnoli," University of Bologna, Bologna, Italy.
  • Terriou L; Division of Hematology, Department of Molecular Biotechnologies and Health Sciences University of Torino/AOU "Città della Salute e della Scienza di Torino," Turin, Italy.
  • Sato Y; Department of Internal Medicine-Hematology, Hôpital Claude Huriez-CHRU Lille, Lille, France.
  • Simpson D; Division of Pathophysiology, Okayama University Graduate School of Health Sciences, Okayama, Japan.
  • Wong R; North Shore Hospital, Auckland, New Zealand.
  • Rossi JF; Sir Y. K. Pao Centre for Cancer and Department of Medicine & Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
  • Nasta S; Department of Hematology, CHU de Montpellier, INSERM U1040, Université Montpellier I, Montpellier, France.
  • Yoshizaki K; Division of Hematology/Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Kurzrock R; Department of Organic Fine Chemicals, The Institute of Scientific and Industrial Research, Osaka University, Osaka, Japan.
  • Uldrick TS; Center for Personalized Therapy and Clinical Trials Office, UC San Diego Moore's Cancer Center, La Jolla, CA.
  • Casper C; Fred Hutch Global Oncology, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Oksenhendler E; Infectious Disease Research Institute, Departments of Medicine and Global Health, University of Washington, Seattle, WA; and.
  • Fajgenbaum DC; Department of Clinical Immunology, Hôpital Saint-Louis, Paris, France.
Blood ; 132(20): 2115-2124, 2018 11 15.
Article em En | MEDLINE | ID: mdl-30181172
Castleman disease (CD) describes a group of heterogeneous hematologic disorders with characteristic histopathological features. CD can present with unicentric or multicentric (MCD) regions of lymph node enlargement. Some cases of MCD are caused by human herpesvirus-8 (HHV-8), whereas others are HHV-8-negative/idiopathic (iMCD). Treatment of iMCD is challenging, and outcomes can be poor because no uniform treatment guidelines exist, few systematic studies have been conducted, and no agreed upon response criteria have been described. The purpose of this paper is to establish consensus, evidence-based treatment guidelines based on the severity of iMCD to improve outcomes. An international Working Group of 42 experts from 10 countries was convened by the Castleman Disease Collaborative Network to establish consensus guidelines for the management of iMCD based on published literature, review of treatment effectiveness for 344 cases, and expert opinion. The anti-interleukin-6 monoclonal antibody siltuximab (or tocilizumab, if siltuximab is not available) with or without corticosteroids is the preferred first-line therapy for iMCD. In the most severe cases, adjuvant combination chemotherapy is recommended. Additional agents are recommended, tailored by disease severity, as second- and third-line therapies for treatment failures. Response criteria were formulated to facilitate the evaluation of treatment failure or success. These guidelines should help treating physicians to stratify patients based on disease severity in order to select the best available therapeutic option. An international registry for patients with CD (ACCELERATE, #NCT02817997) was established in October 2016 to collect patient outcomes to increase the evidence base for selection of therapies in the future.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperplasia do Linfonodo Gigante / Corticosteroides / Anticorpos Monoclonais / Antineoplásicos Tipo de estudo: Clinical_trials / Guideline / Systematic_reviews Limite: Humans Idioma: En Revista: Blood Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperplasia do Linfonodo Gigante / Corticosteroides / Anticorpos Monoclonais / Antineoplásicos Tipo de estudo: Clinical_trials / Guideline / Systematic_reviews Limite: Humans Idioma: En Revista: Blood Ano de publicação: 2018 Tipo de documento: Article