Evidence map›Paper›PMID 25833390›Full record

Trial reportBritish journal of haematology2015

A phase 2 study of bortezomib in combination with ifosfamide/vinorelbine in paediatric patients and young adults with refractory/recurrent Hodgkin lymphoma: a Children's Oncology Group study.

Terzah M Horton, Richard A Drachtman, Lu Chen, Peter D Cole, Kathleen McCarten, Stephan Voss, Robert P Guillerman, Allen Buxton, Scott C Howard, Shirley M Hogan and 9 more

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

Trial report in British journal of haematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

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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

19 authors at 11 institutions in 1 country.

Terzah M HortonDepartment of Pediatrics, Division of Pediatric Haematology-Oncology, Texas Children's Cancer Center and Baylor College of Medicine, Houston, TX, USA.
Richard A DrachtmanUMDNJ-Robert Wood Johnson Medical School, Brunswick, NJ, USA.
Lu ChenChildren's Oncology Group, Statistics and Data Center, Monrovia, CA, USA.
Peter D ColeDepartment of Pediatrics, The Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA.
Kathleen McCartenQuality Assurance Response Centre (QARC), Brown University, Providence, RI, USA.
Stephan VossBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Robert P GuillermanDepartment of Pediatric Radiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Allen BuxtonChildren's Oncology Group, Statistics and Data Center, Monrovia, CA, USA.
Scott C HowardDepartment of Oncology, St. Jude's Children's Research Hospital, Memphis, TN, USA.
Shirley M HoganDepartment of Pharmacy, University of Mississippi, Jackson, MS, USA.
Andrea M SheehanDepartment of Pathology, Texas Children's Hospital and Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Dolores López-TerradaDepartment of Pathology, Texas Children's Hospital and Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Matthew D MrazekDepartment of Pediatrics, Division of Pediatric Haematology-Oncology, Texas Children's Cancer Center and Baylor College of Medicine, Houston, TX, USA.
Neeraj AgrawalDepartment of Pediatrics, Division of Pediatric Haematology-Oncology, Texas Children's Cancer Center and Baylor College of Medicine, Houston, TX, USA.
Meng-Fen WuDivision of Biostatistics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Hao LiuDivision of Biostatistics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Pedro A De AlarconSt. Jude Midwest Affiliate, Peoria, IL, USA.
Tanya M TrippetMemorial Sloan-Kettering Cancer Centre, New York, NY, USA.
Cindy L SchwartzDepartment of Pediatrics, MD Anderson Cancer Center, Houston, TX, USA.
Baylor College of Medicine · USChildren's Cancer Center · USChildren's Oncology Group · USAlbert Einstein College of Medicine · USBrown University · USHarvard University · USJohnson University · USMemorial Sloan Kettering Cancer Center · USSt. Jude Children's Research Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity of Mississippi · 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
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ANDERSON, JAMES R · 2003 to 2013
$67.5M
Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, HELEN E HESLOP · 2007 to 2026
$51.4M
QUALITY ASSURANCE REVIEW CENTER (QARC)U10CA029511 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FITZGERALD, THOMAS J. · 1985 to 2013
$23.4M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
Identifying Cell Stress Proteins that Predict Clinical Response in Pediatric AMLR01CA164024 · NCI · BAYLOR COLLEGE OF MEDICINE · PI HORTON, TERZAH M · 2013 to 2017
$1.7M
Proteosome Inhibition Therapy for Hematologic MalignancyK23CA113775 · NCI · BAYLOR COLLEGE OF MEDICINE · PI HORTON, TERZAH M · 2006 to 2010
$670k
NCI NIH HHS CA113775NCI NIH HHS CA125123NCI NIH HHS K23 CA113775NCI NIH HHS P30 CA125123NCI NIH HHS P50 CA126752NCI NIH HHS P50CA126752NCI NIH HHS R01 CA164024NCI NIH HHS U10 CA029511NCI NIH HHS U10 CA098413NCI NIH HHS U10CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U24 CA114766
6 · The paper itself

Abstract

A Children's Oncology Group clinical trial aimed to determine if bortezomib (B) increased the efficacy of ifosfamide and vinorelbine (IV) in paediatric Hodgkin lymphoma (HL). This study enrolled 26 relapsed HL patients (<30 years) treated with two to four cycles of IVB. The primary endpoint was anatomic complete response (CR) after two cycles. Secondary endpoints included overall response (OR: CR + partial response) at study completion compared to historical controls [72%; 95% confidence interval (CI): 59-83%]. Although few patients achieved the primary objective, OR with IVB improved to 83% (95% CI: 61-95%; p = 0.32). Although not statistically different, results suggest IVB may be a promising combination.

Indexed as

AdultAntineoplastic Combined Chemotherapy ProtocolsBoronic AcidsBortezomibChildChild, PreschoolDisease-Free SurvivalHodgkin DiseaseHumansIfosfamideNeoplasm Recurrence, LocalPyrazinesVinblastineVinorelbineYoung AdultBoronic AcidsBortezomibIfosfamidePyrazinesVinblastineVinorelbinechildhood haematological malignanciesclinical trialsNF-κBpaediatric oncology

Identifiers

PMID25833390
PMCPMC4478135
OpenAlexW2124658474

What OpenQuestion holds

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Registered trials

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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.