Treatment outcome in early diffuse cutaneous systemic sclerosis: the European Scleroderma Observational Study (ESOS). Issue 7 (10th February 2017)
- Record Type:
- Journal Article
- Title:
- Treatment outcome in early diffuse cutaneous systemic sclerosis: the European Scleroderma Observational Study (ESOS). Issue 7 (10th February 2017)
- Main Title:
- Treatment outcome in early diffuse cutaneous systemic sclerosis: the European Scleroderma Observational Study (ESOS)
- Authors:
- Herrick, Ariane L
Pan, Xiaoyan
Peytrignet, Sébastien
Lunt, Mark
Hesselstrand, Roger
Mouthon, Luc
Silman, Alan
Brown, Edith
Czirják, László
Distler, Jörg H W
Distler, Oliver
Fligelstone, Kim
Gregory, William J
Ochiel, Rachel
Vonk, Madelon
Ancuţa, Codrina
Ong, Voon H
Farge, Dominique
Hudson, Marie
Matucci-Cerinic, Marco
Balbir-Gurman, Alexandra
Midtvedt, Øyvind
Jordan, Alison C
Jobanputra, Paresh
Stevens, Wendy
Moinzadeh, Pia
Hall, Frances C
Agard, Christian
Anderson, Marina E
Diot, Elisabeth
Madhok, Rajan
Akil, Mohammed
Buch, Maya H
Chung, Lorinda
Damjanov, Nemanja
Gunawardena, Harsha
Lanyon, Peter
Ahmad, Yasmeen
Chakravarty, Kuntal
Jacobsen, Søren
MacGregor, Alexander J
McHugh, Neil
Müller-Ladner, Ulf
Riemekasten, Gabriela
Becker, Michael
Roddy, Janet
Carreira, Patricia E
Fauchais, Anne Laure
Hachulla, Eric
Hamilton, Jennifer
İnanç, Murat
McLaren, John S
van Laar, Jacob M
Pathare, Sanjay
Proudman, Susannah
Rudin, Anna
Sahhar, Joanne
Coppere, Brigitte
Serratrice, Christine
Sheeran, Tom
Veale, Douglas J
Grange, Claire
Trad, Georges-Selim
Denton, Christopher P
… (more) - Abstract:
- Abstract : Objectives: The rarity of early diffuse cutaneous systemic sclerosis (dcSSc) makes randomised controlled trials very difficult. We aimed to use an observational approach to compare effectiveness of currently used treatment approaches. Methods: This was a prospective, observational cohort study of early dcSSc (within three years of onset of skin thickening). Clinicians selected one of four protocols for each patient: methotrexate, mycophenolate mofetil (MMF), cyclophosphamide or 'no immunosuppressant'. Patients were assessed three-monthly for up to 24 months. The primary outcome was the change in modified Rodnan skin score (mRSS). Confounding by indication at baseline was accounted for using inverse probability of treatment (IPT) weights. As a secondary outcome, an IPT-weighted Cox model was used to test for differences in survival. Results: Of 326 patients recruited from 50 centres, 65 were prescribed methotrexate, 118 MMF, 87 cyclophosphamide and 56 no immunosuppressant. 276 (84.7%) patients completed 12 and 234 (71.7%) 24 months follow-up (or reached last visit date). There were statistically significant reductions in mRSS at 12 months in all groups: −4.0 (−5.2 to −2.7) units for methotrexate, −4.1 (−5.3 to −2.9) for MMF, −3.3 (−4.9 to −1.7) for cyclophosphamide and −2.2 (−4.0 to −0.3) for no immunosuppressant (p value for between-group differences=0.346). There were no statistically significant differences in survival between protocols before (p=0.389) or afterAbstract : Objectives: The rarity of early diffuse cutaneous systemic sclerosis (dcSSc) makes randomised controlled trials very difficult. We aimed to use an observational approach to compare effectiveness of currently used treatment approaches. Methods: This was a prospective, observational cohort study of early dcSSc (within three years of onset of skin thickening). Clinicians selected one of four protocols for each patient: methotrexate, mycophenolate mofetil (MMF), cyclophosphamide or 'no immunosuppressant'. Patients were assessed three-monthly for up to 24 months. The primary outcome was the change in modified Rodnan skin score (mRSS). Confounding by indication at baseline was accounted for using inverse probability of treatment (IPT) weights. As a secondary outcome, an IPT-weighted Cox model was used to test for differences in survival. Results: Of 326 patients recruited from 50 centres, 65 were prescribed methotrexate, 118 MMF, 87 cyclophosphamide and 56 no immunosuppressant. 276 (84.7%) patients completed 12 and 234 (71.7%) 24 months follow-up (or reached last visit date). There were statistically significant reductions in mRSS at 12 months in all groups: −4.0 (−5.2 to −2.7) units for methotrexate, −4.1 (−5.3 to −2.9) for MMF, −3.3 (−4.9 to −1.7) for cyclophosphamide and −2.2 (−4.0 to −0.3) for no immunosuppressant (p value for between-group differences=0.346). There were no statistically significant differences in survival between protocols before (p=0.389) or after weighting (p=0.440), but survival was poorest in the no immunosuppressant group (84.0%) at 24 months. Conclusions: These findings may support using immunosuppressants for early dcSSc but suggest that overall benefit is modest over 12 months and that better treatments are needed. Trial registration number: NCT02339441. … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 76:Issue 7(2017)
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 76:Issue 7(2017)
- Issue Display:
- Volume 76, Issue 7 (2017)
- Year:
- 2017
- Volume:
- 76
- Issue:
- 7
- Issue Sort Value:
- 2017-0076-0007-0000
- Page Start:
- 1207
- Page End:
- 1218
- Publication Date:
- 2017-02-10
- Subjects:
- Systemic Sclerosis -- Treatment -- Cyclophosphamide -- Methotrexate
Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2016-210503 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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