Evidence map›Paper›PMID 30283148›Full record

ArticleBone marrow transplantation2019

Current use of biosimilar G-CSF for haematopoietic stem cell mobilisation.

Simon Pahnke, Torstein Egeland, Jörg Halter, Hans Hägglund, Bronwen E Shaw, Ann E Woolfrey, Jeff Szer, Working Group Medical of the World Marrow Donor Association

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Observational
  5. Review
  6. Current state and future opportunities in granulocyte colony-stimulating factor (G-CSF).Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2022
    Article
  7. Regulatory Evaluation of Biosimilars: Refinement of Principles Based on the Scientific Evidence and Clinical Experience.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2022
    Review
  8. Observational
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Extrapolation in Practice: Lessons from 10 Years with Biosimilar Filgrastim.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2019
    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

8 authors at 6 institutions in 5 countries.

Simon PahnkeDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden. simon.pahnke@medsci.uu.se.ORCID http://orcid.org/0000-0002-3541-2027
Torstein EgelandInstitute of Immunology, Oslo University Hospital-Rikshospitalet and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Jörg HalterDepartment of Hematology, University Hospital Basel and University of Basel, Basel, Switzerland.
Hans HägglundDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Bronwen E ShawCentre for International Blood and Bone Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Ann E WoolfreyDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Jeff SzerIntegrated Haematology Department, Victorian Comprehensive Cancer Centre, Royal Melbourne Hospital, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-6783-2301
Working Group Medical of the World Marrow Donor Association
Uppsala University · SEMedical College of Wisconsin · USOslo University Hospital · NOThe Royal Melbourne Hospital · AUUniversity of Basel · CHUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite biosimilars of the granulocyte-colony stimulating factor (G-CSF) filgrastim being approved by the European Medicines Agency since 2008, there is still some debate regarding their use in related and unrelated healthy haematopoietic stem cell donors. We present a review of published experiences using biosimilar filgrastim for healthy donor mobilisation as well as the results of a survey by the World Marrow Donor Association (WMDA) of its current use by register-associated transplant and collection centres for both related and unrelated donors. A total of 1287 healthy donors and volunteers are included in the reviewed studies. The pharmacokinetics and pharmacodynamics studies show a high degree of similarity to the reference product Neupogen. Mobilisation of CD34 + cells as well as reported adverse events are also found to be comparable, although there is still a lack of long-term follow up for both Neupogen and filgrastim biosimilars. No evidence is found of a higher risk of filgrastim antibody formation using filgrastim biosimilars. Based on this increased experience, the WMDA therefore recommend that Stem Cell Donor Registries can use filgrastim biosimilars for the mobilisation of peripheral blood progenitor cells in healthy donors, provided that they are approved by national and/or regional agencies.

Indexed as

FemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHumansMaleTissue DonorsGranulocyte Colony-Stimulating Factor

Identifiers

PMID30283148
OpenAlexW2895028112

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.