Evidence map›Paper›PMID 33299233›Full record

ArticleHaematologica2022

Pre-existing antibodies against polyethylene glycol reduce asparaginase activities on first administration of pegylated E. coli asparaginase in children with acute lymphocytic leukemia.

Alaeddin Khalil, Gudrun Würthwein, Jana Golitsch, Georg Hempel, Manfred Fobker, Joachim Gerss, Anja Möricke, Martin Zimmermann, Petr Smisek, Massimo Zucchetti and 9 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Observational
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Adverse Impacts of PEGylated Protein Therapeutics: A Targeted Literature Review.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Comment on Ammonia level as a proxy of asparaginase inactivation in children: A strategy for classification of infusion reactions.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2021
    Article
  20. Potential mechanisms of anaphylaxis to COVID-19 mRNA vaccines.The Journal of allergy and clinical immunology · 2021
    Review
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 13 institutions in 8 countries.

Alaeddin KhalilDepartment of Pediatric Hematology and Oncology, University Children's Hospital Muenster.
Gudrun WürthweinDepartment of Pediatric Hematology and Oncology, University Children's Hospital Muenster.
Jana GolitschDepartment of Pediatric Hematology and Oncology, University Children's Hospital Muenster.
Georg HempelDepartment of Pharmaceutical and Medical Chemistry, Clinical Pharmacy, University of Muenster.
Manfred FobkerCenter of Laboratory Medicine, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149 Muenster.
Joachim GerssInstitute of Biostatistics and Clinical Research, University of Muenster.
Anja MörickeDepartment of Pediatrics, University Medical Center Schleswig-Holstein, Campus Kiel, Kiel.
Martin ZimmermannDepartment of Pediatric Hematology and Oncology, Medical School Hannover.
Petr SmisekDepartment of Pediatric Hematology and Oncology, University Hospital Motol, Praha, Czech Republic.
Massimo ZucchettiLaboratory of Cancer Pharmacology, Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan.
Christa NathDepartments of Biochemistry and Oncology, The Children's Hospital at Westmead, Sydney Pharmacy School, University of Sydney, Sydney.
Andishe AttarbaschiDepartment of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna.
Arend Von StackelbergDepartments of Pediatric Oncology/Hematology and of General Pediatrics, Charité - University Medicine Berlin, Berlin.
Nicola GökbugetDepartment of Medicine, University Hospital, Frankfurt a.M.
Carmelo RizzariPediatric Hematology-Oncology Unit, Department of Pediatrics, University of Milano-Bicocca, MBBM Foundation, ASST-Monza, Monza.
Valentino ConterPediatric Hematology-Oncology Unit, Department of Pediatrics, University of Milano-Bicocca, MBBM Foundation, ASST-Monza, Monza.
Martin SchrappeDepartment of Pediatrics, University Medical Center Schleswig-Holstein, Campus Kiel, Kiel.
Joachim BoosDepartment of Pediatric Hematology and Oncology, University Children's Hospital Muenster.
Claudia Lanvers-KaminskyDepartment of Pediatric Hematology and Oncology, University Children's Hospital Muenster. lanvers@uni-muenster.de.
Children's Clinical University Hospital · LVUniversity Hospital and Clinics · USUniversity of Milano-Bicocca · ITUniwersytecki Szpital Dziecięcy · PLCharité - Universitätsmedizin Berlin · DEChildren's Hospital at Westmead · AUMario Negri Institute for Pharmacological Research · ITMedizinische Hochschule Hannover · DESt Anna Children's Hospital · ATUniversity Hospital Frankfurt · DEUniversity Hospital in Motol · CZUniversity Hospital Münster · DEUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies against polyethylene glycol (PEG) in healthy subjects raise concerns about the efficacy of pegylated drugs. We evaluated the prevalence of antibodies against PEG among patients with acute lymphoblastic leukemia (ALL) prior to and/or immediately after their first dose of pegylated E.coli asparaginase (PEG-ASNase). Serum samples of 701 children, 673 with primary ALL, 28 with relapsed ALL, and 188 adults with primary ALL were analyzed for anti-PEG IgG and IgM. Measurements in 58 healthy infants served as reference to define cut-points for antibody-positive and -negative samples. Anti-PEG antibodies were detected in ALL patients prior the first PEG-ASNase with a prevalence of 13.9% (anti-PEG IgG) and 29.1% (anti-PEG IgM). After administration of PEG-ASNase the prevalence of anti-PEG antibodies decreased to 4.2% for anti-PEG IgG and to 4.5% for anti-PEG IgM. Pre-existing anti-PEG antibodies did not inhibit PEG-ASNase activity but significantly reduced PEGASNase activity levels in a concentration dependent manner. Although pre-existing anti-PEG antibodies did not boost, pre-existing anti-PEG IgG were significantly associated with firstexposure hypersensitivity reactions (CTCAE grade 2) (p.

Indexed as

Antineoplastic AgentsPrecursor Cell Lymphoblastic Leukemia-LymphomaAdultAntibodiesAsparaginaseChildEscherichia coliHumansInfantPolyethylene GlycolsAntibodiesAntineoplastic AgentsAsparaginasePolyethylene Glycols

Identifiers

PMID33299233
PMCPMC8719085
OpenAlexW3112842577

What OpenQuestion holds

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LicenceCC BY-NC
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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.