Protection against disease and treatment toxicity

Investigating novel treatment options in Systemic Sclerosis

2024-06-14

(Press-News.org) Autologous hematopoietic stem cell transplantation (aHSCT) for SSc has been proven the most effective treatment strategy with regard to overall and event free survival in selected patients.2 But a key limitation is its toxicity, and new treatment options are needed. Two abstracts presented at the 2024 EULAR congress in Vienna focused on novel approaches.

Jörg Henes presented on behalf of the AST MOMA investigators. This prospective, open-label, study evaluated the feasibility of aHSCT in patients with impaired lung or heart function, and also assessed the efficacy of a reduced-toxicity regimen. Patients were stratified according to their manifestations, and mobilisation was conducted with reduced (2x 1000 mg) cyclophosphamide plus lenograstim before CD34+ selection. For patients with active alveolitis, cyclophosphamide was increased to 2 x 1500 mg, and those with functional heart involvement received a conditioning regimen with thiotepa, a half dose of cyclophosphamide, and rATG before reinfusion of the selected stem cells. The primary endpoint was overall survival.

Over 3-year follow-up, 8 of the 35 included patients died. The overall response rate was 71.4% after 12 months and 60% after 36 months. Progressive disease was reported in 4 patients, and 1 relapsed during the first year – whereas 4 others relapsed at a later time point. Overall, the primary endpoint was reached, since the overall survival rate after 3 years was comparable to available data.3 The treatment-related mortality rate of 11.4% was higher than the researchers had expected, but could be attributed to a high-risk population – being predominately male, with functional cardiac involvement, and over 90% having diffuse cutaneous disease. The authors believe this is the first prospective study using a reduced cyclophosphamide mobilising and conditioning regimen in patients with cardiac involvement, and it is impressive that this reduced-toxicity regimen showed a comparable outcome regarding the overall survival.

Within the same session, Panagiota Xanthouli presented new data from the EDITA trial, focusing on patients with SSc and mild pulmonary arterial hypertension (PAH) treated with ambrisentan. Previous data show this option delivered a significant decline of pulmonary vascular resistance (PVR) but not of mean pulmonary arterial pressure (mPAP) versus placebo after 6 months.4 The current study aimed to assess the long-term effects of continued therapy with ambrisentan versus a control group which received no vasodilative treatment. The primary endpoint was to assess whether continued treatment with ambrisentan prevented the development of PAH according to the new definition.5

The results revealed significant improvement of mPAP in the group receiving ambrisentan versus control. Additionally, 4 patients in the control group developed new PAH with mPAP >20 mmHg, compared to none of the patients receiving ambrisentan. This suggests that continued targeted PAH therapy protects patients with SSc from deteriorating haemodynamics.

Taken together, these new findings could have an important bearing on the current standard of care for patients with SSc.

Source

Pecher AC, et al. Highdose Chemotherapy and transplantation of 34+ selected stem cells for progressive systemic sclerosis with or without cardiac involvement or alveolitis - Modification according to manifestation (AST MOMA). Presented at EULAR 2024; OP0212.

Ann Rheum Dis 2024; DOI: 10.1136/annrheumdis-2024-eular.1742.

Xanthouli P, et al. Effect of treatment with ambrisentan in patients with systemic sclerosis and mild pulmonary arterial hypertension: long-term follow-up data from EDITA study. Presented at EULAR 2024; OP0241.

Ann Rheum Dis 2024; DOI: 10.1136/annrheumdis-2024-eular.1986.

References

1. Del Galdo F, et al. 2023 UPDATE OF EULAR RECOMMENDATIONS FOR THE TREATMENT OF SYSTEMIC SCLEROSIS. Presented at EULAR 2023; OP0234.

2. van Laar JM, et al. Autologous hematopoietic stem cell transplantation vs intravenous pulse cyclophosphamide in diffuse cutaneous systemic sclerosis: a randomized clinical trial. JAMA 2014;311(24):2490–8.

3. Farge D, et al. Autologous hematopoietic stem cell transplantation for autoimmune diseases: an observational study on 12 years' experience from the European Group for Blood and Marrow Transplantation Working Party on Autoimmune Diseases. Haematologica 2010;95(2):284–92.

4. Pan Z, et al. Early treatment with ambrisentan of mildly elevated mean pulmonary arterial pressure associated with systemic sclerosis: a randomized, controlled, double-blind, parallel group study (EDITA study). Arthritis Res Ther 2019;21(1):217.

5. Humbert M, et al. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Heart J 2022;43(38):3618–731.

About EULAR

EULAR is the European umbrella organisation representing scientific societies, health professional associations and organisations for people with rheumatic and musculoskeletal diseases (RMDs). EULAR aims to reduce the impact of RMDs on individuals and society, as well as improve RMD treatments, prevention, and rehabilitation. To this end, EULAR fosters excellence in rheumatology education and research, promotes the translation of research advances into daily care, and advocates for the recognition of the needs of those living with RMDs by EU institutions.

Contact

EULAR Communications, communications@eular.org

Notes to Editors

EULAR Recommendations

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