Evidence map›Paper›PMID 33823167›Full record

ArticleTransplantation and cellular therapy2021

Myeloablative Busulfan/Melphalan Consolidation following Induction Chemotherapy for Patients with Newly Diagnosed High-Risk Neuroblastoma: Children's Oncology Group Trial ANBL12P1.

M Meaghan Granger, Arlene Naranjo, Rochelle Bagatell, Steven G DuBois, Jeannine S McCune, Sheena C Tenney, Brian D Weiss, Yael P Mosse, Shahab Asgharzadeh, Stephen A Grupp and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 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

22 authors at 16 institutions in 2 countries.

M Meaghan GrangerDepartment of Pediatrics, Cook Children's Medical Center, Fort Worth, Texas. Electronic address: Meaghan.GrangerMD@cookchildrens.org.
Arlene NaranjoChildren's Oncology Group Statistics & Data Center, Department of Biostatistics, University of Florida, Gainesville, Florida.
Rochelle BagatellDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Steven G DuBoisDana-Farber / Boston Children's Cancer and Blood Disorder Center and Harvard Medical School, Boston, Massachusetts.
Jeannine S McCuneDepartment of Population Sciences, City of Hope, Duarte, California.
Sheena C TenneyChildren's Oncology Group Statistics & Data Center, Department of Biostatistics, University of Florida, Gainesville, Florida.
Brian D WeissDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Yael P MosseDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Shahab AsgharzadehDepartment of Pediatrics, Children's Hospital of Los Angeles, Los Angeles, California.
Stephen A GruppDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Michael D HogartyDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Julie M Gastier-FosterInstitute for Genomic Medicine, Nationwide Children's Hospital and Departments of Pathology and Pediatrics, Ohio State University College of Medicine, Columbus, Ohio.
Denise MillsDepartment of Nursing, Hospital for Sick Children, Toronto, Ontario, Canada.
Barry L ShulkinDepartment of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
Marguerite T ParisiDepartments of Radiology, Seattle Children's Hospital/University of Washington School of Medicine, Seattle, Washington.
Wendy B LondonDana-Farber / Boston Children's Cancer and Blood Disorder Center and Harvard Medical School, Boston, Massachusetts.
John Han-ChangDepartment of Radiation Oncology, University of Oklahoma Health Science Center, Oklahoma City, Oklahoma.
Joseph PanoffDepartment of Radiation Oncology, Miami Cancer Institute, Baptist Health South Florida.
Daniel von AllmenDepartment of Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Jason A JarzembowskiDepartment of Pathology, Midwest Children's Cancer Center, Milwaukee, Wisconsin.
Julie R ParkDepartments of Pediatrics, Seattle Children's Hospital/University of Washington School of Medicine, Seattle, Washington.
Gregory A YanikDepartment of Pediatrics, University of Michigan Medical Center, Ann Arbor, Michigan.
University of Pennsylvania · USCincinnati Children's Hospital Medical Center · USHarvard University · USUniversity of Florida · USBaptist Health South Florida · USChildren's Cancer Center · USChildren's Hospital of Los Angeles · USChildren's Hospital of Philadelphia · USCity of Hope · USCook Children's Medical Center · USHospital for Sick Children · CANationwide Children's Hospital · USSeattle Children's Hospital · USSt. Jude Children's Research Hospital · USUniversity of Michigan–Ann Arbor · USUniversity of Oklahoma Health Sciences Center · 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
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
QUALITY ASSURANCE REVIEW CENTER (QARC)U10CA029511 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FITZGERALD, THOMAS J. · 1985 to 2013
$23.4M
Optimizing Busulfan: Efficacy, Toxicity, and PharmacometabolomicsR01CA182963 · NCI · UNIVERSITY OF WASHINGTON · PI MCCUNE, JEANNINE S · 2014 to 2018
$2.5M
NCI NIH HHS R01 CA182963NCI NIH HHS U10 CA029511NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

Consolidation using high-dose chemotherapy with autologous stem cell transplantation (ASCT) is an important component of frontline therapy for children with high-risk neuroblastoma. The optimal preparative regimen is uncertain, although recent data support a role for busulfan/melphalan (BuMel). The Children's Oncology Group (COG) conducted a trial (ANBL12P1) to assess the tolerability and feasibility of BuMel ASCT following a COG induction. Patients with newly diagnosed high-risk neuroblastoma who did not progress during induction therapy and met organ function requirements received i.v. busulfan (every 24 hours for 4 doses based on age and weight) and melphalan (140 mg/m

Indexed as

Hematopoietic Stem Cell TransplantationNeuroblastomaBusulfanChildHumansInduction ChemotherapyMelphalanTransplantation, AutologousBusulfanMelphalanBusulfanMelphalanNeuroblastomaPharmacokineticsSinusoidal obstruction syndromeTransplantation

Identifiers

PMID33823167
PMCPMC8855886
OpenAlexW3134469664

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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.