Literature DB >> 22072024

Current state of evidence on 'off-label' therapeutic options for systemic lupus erythematosus, including biological immunosuppressive agents, in Germany, Austria and Switzerland--a consensus report.

M Aringer1, H Burkhardt, G R Burmester, R Fischer-Betz, M Fleck, W Graninger, F Hiepe, A M Jacobi, I Kötter, H J Lakomek, H M Lorenz, B Manger, G Schett, R E Schmidt, M Schneider, H Schulze-Koops, J S Smolen, C Specker, T Stoll, A Strangfeld, H P Tony, P M Villiger, R Voll, T Witte, T Dörner.   

Abstract

Systemic lupus erythematosus (SLE) can be a severe and potentially life-threatening disease that often represents a therapeutic challenge because of its heterogeneous organ manifestations. Only glucocorticoids, chloroquine and hydroxychloroquine, azathioprine, cyclophosphamide and very recently belimumab have been approved for SLE therapy in Germany, Austria and Switzerland. Dependence on glucocorticoids and resistance to the approved therapeutic agents, as well as substantial toxicity, are frequent. Therefore, treatment considerations will include 'off-label' use of medication approved for other indications. In this consensus approach, an effort has been undertaken to delineate the limits of the current evidence on therapeutic options for SLE organ disease, and to agree on common practice. This has been based on the best available evidence obtained by a rigorous literature review and the authors' own experience with available drugs derived under very similar health care conditions. Preparation of this consensus document included an initial meeting to agree upon the core agenda, a systematic literature review with subsequent formulation of a consensus and determination of the evidence level followed by collecting the level of agreement from the panel members. In addition to overarching principles, the panel have focused on the treatment of major SLE organ manifestations (lupus nephritis, arthritis, lung disease, neuropsychiatric and haematological manifestations, antiphospholipid syndrome and serositis). This consensus report is intended to support clinicians involved in the care of patients with difficult courses of SLE not responding to standard therapies by providing up-to-date information on the best available evidence.

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Year:  2011        PMID: 22072024     DOI: 10.1177/0961203311426569

Source DB:  PubMed          Journal:  Lupus        ISSN: 0961-2033            Impact factor:   2.911


  24 in total

1.  Connective tissue disease: Trial of SLE therapies in real-world settings.

Authors:  Manuel Ramos-Casals; Munther A Khamashta
Journal:  Nat Rev Rheumatol       Date:  2012-02-07       Impact factor: 20.543

Review 2.  Challenges and opportunities in targeting the CD28/CTLA-4 pathway in transplantation and autoimmunity.

Authors:  Rebecca L Crepeau; Mandy L Ford
Journal:  Expert Opin Biol Ther       Date:  2017-05-30       Impact factor: 4.388

3.  Allogeneic mesenchymal stem cell transplantation for lupus nephritis patients refractory to conventional therapy.

Authors:  Fei Gu; Dandan Wang; Huayong Zhang; Xuebing Feng; Gary S Gilkeson; Songtao Shi; Lingyun Sun
Journal:  Clin Rheumatol       Date:  2014-08-14       Impact factor: 2.980

4.  [Recipes systemic lupus erythematosus].

Authors:  M Aringer; M Schneider
Journal:  Z Rheumatol       Date:  2014-08       Impact factor: 1.372

Review 5.  [Tapering and termination of immunosuppressive therapy : Systemic lupus erythematosus].

Authors:  M Aringer; N Leuchten; R Fischer-Betz
Journal:  Z Rheumatol       Date:  2017-02       Impact factor: 1.372

6.  Neuropsychiatric Symptoms in Lupus.

Authors:  Maria Gulinello; Jing Wen; Chaim Putterman
Journal:  Psychiatr Ann       Date:  2012-09

7.  [Shared decision making even for complex systemic autoimmune diseases such as Systemic Lupus Erythematosus (SLE)?]

Authors:  M Schneider; H Carnarius; T Schlegl
Journal:  Z Rheumatol       Date:  2017-04       Impact factor: 1.372

Review 8.  Drugs in early clinical development for Systemic Lupus Erythematosus.

Authors:  Mariana Postal; Nailú Angélica Sinicato; Simone Appenzeller; Timothy B Niewold
Journal:  Expert Opin Investig Drugs       Date:  2016-04-07       Impact factor: 6.206

Review 9.  [Established medications : new areas of application].

Authors:  I Kötter; J C Henes
Journal:  Z Rheumatol       Date:  2013-11       Impact factor: 1.372

10.  Retinoic acid-producing, ex-vivo-generated human tolerogenic dendritic cells induce the proliferation of immunosuppressive B lymphocytes.

Authors:  V Di Caro; B Phillips; C Engman; J Harnaha; M Trucco; N Giannoukakis
Journal:  Clin Exp Immunol       Date:  2013-11       Impact factor: 4.330

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