Evidence map›Paper›PMID 28589389›Full record

ArticleZeitschrift fur Rheumatologie2018

[Safety and efficacy of off-label use of biologic therapies in patients with inflammatory rheumatic diseases refractory to standard of care therapy : Data from a nationwide German registry (GRAID2)].

F Proft, H Schulze-Koops, M Grunke, E Schrezenmeier, F Halleck, J Henes, L Unger, E Schmidt, C Fiehn, A Jacobi and 14 more

Abstract read
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In one paragraph

Article in Zeitschrift fur Rheumatologie, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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

24 authors at 17 institutions in 1 country.

F ProftSektion Rheumatologie und Klinische Immunologie, Medizinische Klinik IV, Klinikum der Universität München, München, Deutschland. Fabian.Proft@charite.de.
H Schulze-KoopsSektion Rheumatologie und Klinische Immunologie, Medizinische Klinik IV, Klinikum der Universität München, München, Deutschland.
M GrunkeSektion Rheumatologie und Klinische Immunologie, Medizinische Klinik IV, Klinikum der Universität München, München, Deutschland.
E SchrezenmeierMedizinische Klinik m.S. Nephrologie, Campus Mitte, Charité Universitätsmedizin, Berlin, Deutschland.
F HalleckMedizinische Klinik m.S. Nephrologie, Campus Mitte, Charité Universitätsmedizin, Berlin, Deutschland.
J HenesAbteilung für Onkologie, Hämatologie, klinische Immunologie, Rheumatologie, Pulmologie, Medizinische Klinik II, Universität Tübingen, Tübingen, Deutschland.
L UngerAbteilung für Rheumatologie, I. Medizinische Klinik, Städtisches Klinikum Dresden, Dresden, Deutschland.
E SchmidtKlinik für Dermatologie, Allergologie und Venerologie, Universität zu Lübeck, Lübeck, Deutschland.
C FiehnPraxis für Rheumatologie und klinische Immunologie, Baden-Baden, Deutschland.
A JacobiMedizinische Klinik B, Ruppiner Kliniken, Medizinische Hochschule Brandenburg Theodor Fontane, Neuruppin, Deutschland.
C Iking-KonertKlinik für Nephrologie und Rheumatologie, UKE-Hamburg-Eppendorf und Klinik für Rheumatologie und Immunologie, Klinikum Bad Bramstedt, Bad Bramstedt, Deutschland.
C KneitzKlinik für Innere Medizin II, Rheumatologie und klinische Immunologie, Klinikum Suedstadt Rostock, Rostock, Deutschland.
R E SchmidtKlinik für Immunologie und Rheumatologie, Medizinische Hochschule Hannover, Hannover, Deutschland.
B BannertKlinik für Rheumatologie und Klinische Immunologie, Universitätsklinikum Freiburg, Medizinische Fakultät, Albert-Ludwigs-Universität Freiburg, Freiburg, Deutschland.
R E VollKlinik für Rheumatologie und Klinische Immunologie, Universitätsklinikum Freiburg, Medizinische Fakultät, Albert-Ludwigs-Universität Freiburg, Freiburg, Deutschland.
R Fischer-BetzPoliklinik für Rheumatologie & Hiller-Forschungszentrum, Universitätsklinikum, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Deutschland.
I KötterAbteilung für Onkologie, Hämatologie, klinische Immunologie, Rheumatologie, Pulmologie, Medizinische Klinik II, Universität Tübingen, Tübingen, Deutschland.
H P TonyAbteilung für Rheumatologie und klinische Immunologie, Zentrum für Innere Medizin, Universitätsklinikum Würzburg, Würzburg, Deutschland.
J HolleKlinik für Rheumatologie und Immunologie, Klinikum Bad Bramstedt, Bad Bramstedt, Deutschland.
M AringerMedizinische Klinik und Poliklinik III, Universitätsklinikum und Medizinische Fakultät Carl Gustav Carus an der TU Dresden, Dresden, Deutschland.
A ErlerMedizinische Klinik und Poliklinik III, Universitätsklinikum und Medizinische Fakultät Carl Gustav Carus an der TU Dresden, Dresden, Deutschland.
F BehrensCIRI/Rheumatologie und Fraunhofer Institut IME, Translationale Medizin und Pharmakologie, Universitätsklinikum Goethe Universität Frankfurt am Main, Frankfurt am Main, Deutschland.
G R BurmesterMedizinische Klinik m.S. Rheumatologie und Klinische Immunologie, Campus Mitte, Charité Universitätsmedizin Berlin, Berlin, Deutschland.
T DörnerMedizinische Klinik m.S. Rheumatologie und Klinische Immunologie, Campus Mitte, Charité Universitätsmedizin Berlin, Berlin, Deutschland.
Charité - Universitätsmedizin Berlin · DELMU Klinikum · DEKlinik und Poliklinik für Psychotherapie und Psychosomatik · DEAsklepios Klinik Altona · DEGoethe University Frankfurt · DEHeinrich Heine University Düsseldorf · DEHNO Bad Bramstedt · DEKlinikum Südstadt Rostock · DEMedizinische Hochschule Brandenburg Theodor Fontane · DEMedizinische Hochschule Hannover · DEStädtisches Klinikum Dresden · DEUniversität Hamburg · DEUniversitätsklinikum Würzburg · DEUniversity Medical Center Freiburg · DEUniversity of Freiburg · DEUniversity of Lübeck · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe German Registry of Autoimmune Diseases 2 (GRAID2) is a retrospective, non-interventional, multicenter registry study collecting data from patients with inflammatory, mainly rheumatic diseases refractory to standard of care therapy and treated with an off-label biologic therapy. The retrospective documentation comprised case history, diagnosis, course of disease (including safety and global efficacy). The objective was to evaluate the global clinical outcome and safety of off-label biologic therapy in clinical practice.

resultsData from 311 patients with an overall observation period of 338.5 patient-years were collected. The mean patients age was 47.8 years with 56.9% females. The most frequently documented diagnoses comprised rejection prophylaxis/therapy after renal transplantation (NTX, 18.3%), ANCA-vasculitides (17.4%), systemic lupus erythematosus (SLE, 10.3%), autoinflammatory fever syndromes (8.4%), autoimmune myositis (7.4%) and pemphigus (5.8%). Documented biologic therapies included rituximab (RTX, 70.1%), tocilizumab (TCZ, 9.3%), infliximab (IFX, 7.1%), anakinra (ANK, 5.5%), adalimumab (ADA, 3.5%), etanercept (ETA, 2.3%) and certolizumab (CTZ, 0.6%). After initiation of off-label biologic treatment, tolerability was assessed by the physicians as "very good"/"good" in 95.5%. Altogether, 275 adverse events were documented and of these, 104 were classified as serious adverse events and occurred in 62 patients. In 19 of these patients severe infections (30.6%) were documented, resulting in a rate of 5.6 severe infections per 100 patient years. A total of six deaths were documented, while five of these cases were rated as not related to the biologics treatment. Notably, the use of RTX in patients with small vessel vasculitides and of TCZ in patients with large vessel vasculitides prior to their approval support their relevance in clinical management of patients with severe diseases.

conclusionThe results of this registry together with data of GRAID1 provide evidence that use of off-label biologic therapies in patients with inflammatory rheumatic diseases refractory to conventional treatment did not result in any new safety signal already known for these compounds or subsequently shown by clinical trials in certain entities.

Indexed as

Autoimmune DiseasesBiological TherapyOff-Label UseFemaleHumansMaleRegistriesRetrospective StudiesStandard of CareBiological therapyFever syndromesGRAIDLupusVasculitis

Identifiers

PMID28589389
OpenAlexW2623064104

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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.