Evidence map›Paper›PMID 30181172›Full record

ArticleBlood2018

International, evidence-based consensus treatment guidelines for idiopathic multicentric Castleman disease.

Frits van Rhee, Peter Voorhees, Angela Dispenzieri, Alexander Fosså, Gordan Srkalovic, Makoto Ide, Nikhil Munshi, Stephen Schey, Matthew Streetly, Sheila K Pierson and 32 more

Registry-linked trialAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02817997 (ACCELERATE), which is not on this map. Cited by 251 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
251citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02817997 recruitingnot on this map

ACCELERATE (Advancing Castleman Care With an Electronic Longitudinal Registry, E-Repository, And Treatment/Effectiveness Research): An International Registry for Patients With Castleman Disease

Typeobservational_patient_registrySponsorUniversity of PennsylvaniaRan2016 to 2027Enrolled1,000ConditionsCastleman Disease, Castleman's Disease, Giant Lymph Node Hyperplasia, Angiofollicular Lymph Hyperplasia
3 · Its place in the literature

Who cites it

251 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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191 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

42 authors.

Frits van RheeMyeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR.ORCID 0000-0001-9959-1282
Peter VoorheesDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, NC.
Angela DispenzieriDivision of Hematology/Oncology, Mayo Clinic, Rochester, MN.
Alexander FossåDepartment of Oncology, Oslo University Hospital-Norwegian Radium Hospital, Oslo, Norway.
Gordan SrkalovicHerbert-Herman Cancer Center, Michigan State University College of Human Medicine, Lansing, MI.
Makoto IdeDepartment of Hematology, Takamatsu Red Cross Hospital, Takamatsu, Kagawa, Japan.
Nikhil MunshiDana-Farber Cancer Institute, VA Boston Healthcare System, Harvard Medical School, Boston, MA.
Stephen ScheyGuys and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Matthew StreetlyGuys and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Sheila K PiersonDivision of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Helen L PartridgeDivision of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Sudipto MukherjeeDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
Dustin ShillingDivision of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Katie StoneMyeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR.
Amy GreenwayMyeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR.
Jason RuthDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Mary Jo LechowiczDepartment of Hematology and Medical Oncology, and.
Shanmuganathan ChandrakasanAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University, Atlanta, GA.
Raj JayanthanDepartment of Medicine, Baylor College of Medicine, Houston, TX.
Elaine S JaffeNational Cancer Institute, National Institutes of Health, Bethesda, MD.
Heather LeitchDivision of Hematology, Department of Medicine, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
Naveen PemmarajuDivision of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Amy ChadburnDepartment of Pathology, Weill Cornell Medical College, New York, NY.
Megan S LimDepartment of Pathology and Laboratory Medicine, and.
Kojo S Elenitoba-JohnsonDepartment of Pathology and Laboratory Medicine, and.
Vera KrymskayaPenn Center for Pulmonary Biology, Pulmonary, Allergy, and Critical Care Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Aaron GoodmanDivision of Hematology/Oncology, Department of Medicine, University of California San Diego, La Jolla, CA.
Christian HoffmannUniversity of Schleswig Holstein, Campus Kiel, Kiel, Germany.
Pier Luigi ZinzaniInstitute of Hematology "L. e A. Seràgnoli," University of Bologna, Bologna, Italy.
Simone FerreroDivision of Hematology, Department of Molecular Biotechnologies and Health Sciences University of Torino/AOU "Città della Salute e della Scienza di Torino," Turin, Italy.
Louis TerriouDepartment of Internal Medicine-Hematology, Hôpital Claude Huriez-CHRU Lille, Lille, France.
Yasuharu SatoDivision of Pathophysiology, Okayama University Graduate School of Health Sciences, Okayama, Japan.
David SimpsonNorth Shore Hospital, Auckland, New Zealand.
Raymond WongSir Y. K. Pao Centre for Cancer and Department of Medicine & Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.ORCID 0000-0002-9011-4268
Jean-Francois RossiDepartment of Hematology, CHU de Montpellier, INSERM U1040, Université Montpellier I, Montpellier, France.
Sunita NastaDivision of Hematology/Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Kazuyuki YoshizakiDepartment of Organic Fine Chemicals, The Institute of Scientific and Industrial Research, Osaka University, Osaka, Japan.
Razelle KurzrockCenter for Personalized Therapy and Clinical Trials Office, UC San Diego Moore's Cancer Center, La Jolla, CA.
Thomas S UldrickFred Hutch Global Oncology, Fred Hutchinson Cancer Research Center, Seattle, WA.
Corey CasperInfectious Disease Research Institute, Departments of Medicine and Global Health, University of Washington, Seattle, WA; and.ORCID 0000-0002-3609-661X
Eric OksenhendlerDepartment of Clinical Immunology, Hôpital Saint-Louis, Paris, France.
David C FajgenbaumDivision of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-7367-8184

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI EDWIN ROBERTO ORELLANA · 1988 to 2026
$104.9M
Hematopathology DiagnosisZIABC011070 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$14.5M
mTOR as a Central Regulator of iMCD Pathogenesis and Novel Therapeutic TargetR01HL141408 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Taku Kambayashi · 2018 to 2026
$6.1M
Atlanta Pediatric Scholars ProgramK12HD072245 · NICHD · EMORY UNIVERSITY · PI Shari Barkin · 2012 to 2026
$5.5M
NHLBI NIH HHS R01 HL141408NIAID NIH HHS P30 AI027757NICHD NIH HHS K12 HD072245
6 · The paper itself

Abstract

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.

Indexed as

Adrenal Cortex HormonesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsCastleman DiseaseClinical Trials as TopicCritical IllnessDisease ManagementEvidence-Based MedicineHumansPractice Guidelines as TopicAdrenal Cortex HormonesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic Agentssiltuximabtocilizumab

Identifiers

PMID30181172
PMCPMC6238190

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.