Evidence map›Paper›PMID 25270958›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

TNF-receptor inhibitor therapy for the treatment of children with idiopathic pneumonia syndrome. A joint Pediatric Blood and Marrow Transplant Consortium and Children's Oncology Group Study (ASCT0521).

Gregory A Yanik, Stephan A Grupp, Michael A Pulsipher, John E Levine, Kirk R Schultz, Donna A Wall, Bryan Langholz, Christopher C Dvorak, Keith Alangaden, Rakesh K Goyal and 6 more

Open access · bronzeAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.2field-weighted citation impact, top 3% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 78 citations in OpenAlex.

  1. CALIPSO: A Randomized Controlled Trial of Calfactant for Acute Lung Injury in Pediatric Stem Cell and Oncology Patients.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Trial
  2. Diagnostic and Prognostic Plasma Biomarkers for Idiopathic Pneumonia Syndrome after Hematopoietic Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Trial
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  20. Pulmonary Complications in Pediatric and Adolescent Patients Following Allogeneic Hematopoietic Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 13 institutions in 2 countries.

Gregory A YanikDepartment of Pediatrics, Blood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan. Electronic address: gyanik@umich.edu.
Stephan A GruppDivision of Oncology, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Michael A PulsipherDivision of Hematology and Hematological Malignancies, Primary Children's Hospital, Salt Lake City, Utah.
John E LevineDepartment of Pediatrics, Blood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan.
Kirk R SchultzDepartment of Pediatrics, Pediatric Hematology/Oncology/BMT, British Columbia Children's Hospital and University of British Columbia, Vancouver, British Columbia, Canada.
Donna A WallDepartment of Pediatrics, University of Manitoba, Winnipeg, Manitoba, Canada.
Bryan LangholzChildren's Oncology Group Statistics and Data Center, University of Southern California, Arcadia, California.
Christopher C DvorakDepartment of Pediatrics, UCSF Benioff Children's Hospital, University of California San Francisco, San Francisco, California.
Keith AlangadenDepartment of Pediatrics, Blood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan.
Rakesh K GoyalDivision of Pediatric Hematology-Oncology, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Eric S WhiteDivision of Critical Care and Pulmonary Medicine, University of Michigan, Ann Arbor, Michigan.
Jennifer M ColluraSchool of Pharmacy, Indiana University-Riley Children's Hospital, Indianapolis, Indiana.
Micah A SkeensDepartment of Nursing, Nationwide Children's Hospital, Columbus, Ohio.
Saada EidDivision of Hematology and Oncology, Department of Pediatrics, Case Western Reserve University, School of Medicine, Cleveland, Ohio.
Elizabeth M PierceDivision of Hematology and Oncology, Department of Pediatrics, Case Western Reserve University, School of Medicine, Cleveland, Ohio.
Kenneth R CookeDepartment of Oncology, Sidney Kimmel Cancer Center, Johns Hopkins University, School of Medicine, Baltimore, Maryland.
University of Michigan · USCase Western Reserve University · USChildren's Hospital of Pittsburgh · USJohns Hopkins University · USNationwide Children's Hospital · USPrimary Children's Hospital · USRiley Hospital for Children · USUCSF Benioff Children's Hospital · USUniversity of British Columbia · CAUniversity of Manitoba · CAUniversity of Pennsylvania · USUniversity of Southern California · USUniversity School · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
PULMONARY CELLULAR AND MOLECULAR BIOLOGY TRAININGT32HL007749 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Pickett Dickson · 1993 to 2026
$19.9M
Pediatric Blood and Marrow Transplant ConsortiumU01HL069254 · NHLBI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI PULSIPHER, MICHAEL A · 2001 to 2010
$2.0M
Re-Engineering the Clinical Research EnterpriseN01HC045220 · HC · NATIONAL CHILDHOOD CANCER FOUNDATION · PI REAMAN, GREGORY H · 2004 to 2004
–
ONTOGENY OF AIRWAY SMOOTH MUSCLE FUNCTIONR29HL045220 · NHLBI · KAPI'OLANI MEDICAL CENTER/WOMEN/CHILDRN · PI NAKAMURA, KENNETH T · 1990 to 1994
–
NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NHLBI NIH HHS 2U01HL069254NHLBI NIH HHS N01 HC045220NHLBI NIH HHS N01 HC-45220/HHSN268200425220CNHLBI NIH HHS T32 HL007749NHLBI NIH HHS U01 HL069254
6 · The paper itself

Abstract

Idiopathic pneumonia syndrome (IPS) is an acute, noninfectious lung disorder associated with high morbidity and mortality after hematopoietic cell transplantation. Previous studies have suggested a role for TNFα in the pathogenesis of IPS. We report a multicenter phase II trial investigating a soluble TNF-binding protein, etanercept (Enbrel, Amgen, Thousand Oaks, CA), for the treatment of pediatric patients with IPS. Eligible patients were < 18 years old, within 120 days after transplantation, and with radiographic evidence of a diffuse pneumonitis. All patients underwent a pretherapy broncho-alveolor lavage (BAL) to establish the diagnosis of IPS. Systemic corticosteroids (2.0 mg/kg/day) plus etanercept (.4 mg/kg twice weekly × 8 doses) were administered. Response was defined as survival and discontinuation of supplemental oxygen support by day 28 of study. Thirty-nine patients (median age, 11 years; range, 1 to 17) were enrolled, with 11 of 39 patients nonevaluable because of identification of pathogens from their pretherapy BAL. In the remaining 28 patients, the median fraction of inspired oxygen at study entry was 45%, with 17 of 28 requiring mechanical ventilation. Complete responses were seen in 20 (71%) patients, with a median time to response of 10 days (range, 1 to 24). Response rates were higher for patients not requiring mechanical ventilation at study entry (100% versus 53%, P = .01). Overall survival at 28 days and 1 year after therapy were 89% (95% confidence interval [CI], 70% to 96%) and 63% (95% CI, 42% to 79%), respectively. Plasma levels of proinflammatory cytokines were significantly increased at onset of therapy, subsequently decreasing in responding patients. The addition of etanercept to high-dose corticosteroids was associated with high response rates and survival in children with IPS.

Indexed as

AdolescentAdrenal Cortex HormonesBronchoalveolar Lavage FluidChildChild, PreschoolCytokinesDrug Therapy, CombinationEtanerceptFemaleHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansIdiopathic Interstitial PneumoniasImmunoglobulin GImmunosuppressive AgentsInfantAdrenal Cortex HormonesCytokinesEtanerceptImmunoglobulin GImmunosuppressive AgentsReceptors, Tumor Necrosis FactorBone marrow transplantationEtanerceptIdiopathic pneumonia syndrome

Identifiers

PMID25270958
PMCPMC4286345
OpenAlexW2028833388

What OpenQuestion holds

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Registered trials

None linked

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.