Evidence map›Paper›PMID 31188727›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2019

Antibodies Predict Pegaspargase Allergic Reactions and Failure of Rechallenge.

Yiwei Liu, Colton A Smith, John C Panetta, Wenjian Yang, Lauren E Thompson, Jacob P Counts, Alejandro R Molinelli, Deqing Pei, Nancy M Kornegay, Kristine R Crews and 8 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
11.8field-weighted citation impact, top 1% 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.

NCT00137111 phase3completednot on this map

Total XV - Total Therapy Study XV for Newly Diagnosed Patients With Acute Lymphoblastic Leukemia

TypeinterventionalSponsorSt. Jude Children's Research HospitalRan2000 to 2014Enrolled501ConditionsLymphoblastic Leukemia, AcuteArmsPrednisone, Dexamethasone, Vincristine, Daunorubicin, Doxorubicin, L-asparaginase, PEG-L-asparaginase, Erwinia asparaginase, Methotrexate, Cyclophosphamide, Cytarabine, Etoposide, Mercaptopurine, Imatinib, chemotherapy, intrathecal chemotherapy
NCT00549848 phase3completednot on this map

Total Therapy Study XVI for Newly Diagnosed Patients With Acute Lymphoblastic Leukemia

TypeinterventionalSponsorSt. Jude Children's Research HospitalRan2007 to 2022Enrolled600ConditionsAcute Lymphoblastic LeukemiaArmsPrednisone, Vincristine, Daunorubicin, PEG-L-asparaginase, Erwinia L-asparaginase, Doxorubicin, Cyclophosphamide, Cytarabine, Thioguanine, Clofarabine, Methotrexate, Mercaptopurine, Dexamethasone, Etoposide, Dasatinib
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Lipid nanoparticle-mediated in vivo generation of panCAR immune cells for solid tumor immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. A 12-Step Desensitization Protocol for Calaspargase Pegol-mknl.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article
  16. Article
  17. Adverse Impacts of PEGylated Protein Therapeutics: A Targeted Literature Review.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Yiwei Liu1St Jude Children's Research Hospital, Memphis, TN.
Colton A Smith1St Jude Children's Research Hospital, Memphis, TN.
John C Panetta1St Jude Children's Research Hospital, Memphis, TN.
Wenjian Yang1St Jude Children's Research Hospital, Memphis, TN.
Lauren E Thompson2University of Colorado Anschutz Medical Campus, Aurora, CO.
Jacob P Counts3University of Tennessee Health Science Center, Memphis, TN.
Alejandro R Molinelli1St Jude Children's Research Hospital, Memphis, TN.
Deqing Pei1St Jude Children's Research Hospital, Memphis, TN.
Nancy M Kornegay1St Jude Children's Research Hospital, Memphis, TN.
Kristine R Crews1St Jude Children's Research Hospital, Memphis, TN.
Hope Swanson1St Jude Children's Research Hospital, Memphis, TN.
Cheng Cheng1St Jude Children's Research Hospital, Memphis, TN.
Seth E Karol1St Jude Children's Research Hospital, Memphis, TN.
William E Evans1St Jude Children's Research Hospital, Memphis, TN.
Hiroto Inaba1St Jude Children's Research Hospital, Memphis, TN.
Ching-Hon Pui1St Jude Children's Research Hospital, Memphis, TN.
Sima Jeha1St Jude Children's Research Hospital, Memphis, TN.
Mary V Relling1St Jude Children's Research Hospital, Memphis, TN.
St. Jude Children's Research Hospital · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Tennessee Health Science Center · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
CPML - Project 3: Genome-wide Studies of Adverse EffectsP50GM115279 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI RELLING, MARY V · 2015 to 2019
$15.1M
PHARMACOGENOMICS OF CHILDHOOD LEUKEMIA (ALL)R37CA036401 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI EVANS, WILLIAM E · 1987 to 2014
$9.7M
PROFESSIONAL ONCOLOGY EDUCATION PROGRAMR25CA023944 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SUZANNE A. GRONEMEYER · 1986 to 2026
$8.3M
Glucocorticoids in Lymphoblastic LeukemiaR01CA142665 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI RELLING, MARY V · 2010 to 2020
$4.6M
NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA142665NCI NIH HHS R25 CA023944NCI NIH HHS R37 CA036401NIGMS NIH HHS P50 GM115279
6 · The paper itself

Abstract

purposePegaspargase (PEG-ASP) has largely replaced native PATIENTS AND

methodsPEG-ASP was administered to 598 patients in St Jude's Total XVI study. Results were compared with Total XV study (ClinicalTrials.gov identifiers: NCT00549848 and NCT00137111), which used native L-ASP. Serum samples (n = 5,369) were analyzed for anti-PEG-ASP immunoglobulin G by enzyme-linked immunosorbent assay. Positive samples were tested for anti-polyethylene glycol (PEG) and anti-L-ASP. We analyzed potential risk factors for reactions and associations between antibodies and reactions, rechallenge outcomes, and PEG-ASP pharmacokinetics.

resultsGrade 2 to 4 reactions were less common in the Total XVI study with PEG-ASP (81 [13.5%] of 598) than in the Total XV study with L-ASP (169 [41.2%] of 410;

conclusionLess IT therapy was the only independent clinical risk factor for reactions to PEG-ASP. PEG, and not L-ASP, is the major antigen that causes allergic reactions. Anti-PEG-ASP has utility in predicting and confirming clinical reactions to PEG-ASP as well as in identifying patients who are most likely to experience failure with rechallenge.

Indexed as

AntibodiesAntineoplastic AgentsAsparaginaseFemaleHumansHypersensitivityMalePolyethylene GlycolsRisk FactorsAntibodiesAntineoplastic AgentsAsparaginasepegaspargasePolyethylene Glycols

Identifiers

PMID31188727
PMCPMC6804844
OpenAlexW2952798265

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.