Evidence map›Paper›PMID 32349731›Full record

Observational studyBMC endocrine disorders2020

Ten years with biosimilar rhGH in clinical practice in Sweden - experience from the prospective PATRO children and adult studies.

Elena Lundberg, Berit Kriström, Hichem Zouater, Anna Deleskog, Charlotte Höybye

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in BMC endocrine disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Observational
  6. Review
  7. Review
  8. Article
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

5 authors at 3 institutions in 2 countries.

Elena LundbergInstitute of Clinical Science/Pediatrics, Umeå University, SE-90185, Umeå, Sweden. elena.lundberg@umu.se.
Berit KriströmInstitute of Clinical Science/Pediatrics, Umeå University, SE-90185, Umeå, Sweden.
Hichem ZouaterSandoz Biopharmaceutical, c/o HEXAL AG, Industriestr. 25, D-83607, Holzkirchen, Germany.
Anna DeleskogSandoz A/S, Copenhagen, Denmark.
Charlotte HöybyeDepartment of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.
Umeå University · SEHexal (Germany) · DEKarolinska Institutet · SE

Funding

Sandoz NA
6 · The paper itself

Abstract

backgroundIn 2007, Omnitrope® was the first biosimilar recombinant human growth hormone (rhGH) to be approved in Sweden for treatment in adults and children. Over 10 years' safety and effectiveness data for biosimilar rhGH can now be presented.

methodsPATRO Children and PATRO Adults are multicenter, longitudinal, observational, post-marketing surveillance studies. Eligible patients include children 0-18 years and adults receiving biosimilar rhGH treatment. Adverse events (AEs) are monitored for safety evaluation. Growth variables in children and metabolic data in adults are recorded for effectiveness evaluation.

resultsAs of January 2019, data from 136 children (48% male) were reported from Swedish centers. Mean age in rhGH treatment-naïve patients at study entry (n = 114) was 7.5 years, with mean 3.6 years treatment duration. No severe AEs of diabetes, impaired glucose tolerance, or malignancy were reported. The most frequently reported AE was nasopharyngitis (n = 16 patients). No clinically relevant anti-hGH or neutralizing antibodies were observed. The mean change from baseline in height standard deviation score (SDS) in naïve prepubertal GH deficiency patients was + 0.79 at 1 year, + 1.27 at 2 years, and + 1.55 at 3 years. Data from 293 adults (44% rhGH-naïve, 51% male) were included. Fatigue was the most frequently reported AE (n = 26 patients). The incidence of new neoplasms or existing neoplasm progression was 23.8 patients per 1000 patient-years. Type 2 diabetes mellitus was reported in four patients. At baseline in rhGH-naïve adults, mean (SD) body mass index (BMI) was 29.1 (5.6) kg/m

conclusionsFor the first time, Swedish data from the PATRO Children and Adults studies are presented. The 10-year data suggest that biosimilar rhGH is well tolerated across pediatric and adult indications. Safety and effectiveness were similar to previous reports for other rhGH preparations. These results need to be confirmed in larger cohorts, highlighting the importance of long-term post-marketing studies.

Indexed as

AdolescentAdultAgedAntibodies, NeutralizingBiosimilar PharmaceuticalsBody HeightChildChild, PreschoolCholesterol, HDLCholesterol, LDLDiabetes Mellitus, Type 2Duration of TherapyDwarfism, PituitaryFemaleGlucose IntoleranceGrowth DisordersAntibodies, NeutralizingBiosimilar PharmaceuticalsCholesterol, HDLCholesterol, LDLGrowth HormoneHuman Growth HormoneRecombinant ProteinsAntibodiesEffectivenessOmnitropeRecombinant growth hormoneSafety

Identifiers

PMID32349731
PMCPMC7191769
OpenAlexW3021867083

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.