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SAT0463 Initial Therapy with an Endothelin Receptor Antagonist (ERA) is Associated with Worse Outcomes in Patients with Systemic Sclerosis and Pulmonary Arterial Hypertension: Observations from the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma Cohort (Pharos)
  1. M.R. Lammi1,
  2. L.A. Saketkoo2,
  3. S.C. Mathai3,
  4. R.T. Domsic4,
  5. V. Steen5,
  6. D.E. Furst6
  7. on behalf of the PHAROS Investigators
  1. 1Louisiana State University
  2. 2UMC Scleroderma and Sarcoidosis Patient Care and Research Center, Tulane University, New Orleans
  3. 3Johns Hopkins School of Medicine, Baltimore
  4. 4University of Pittsburgh Medical Center, Pittsburgh
  5. 5Georgetown University, Washington DC
  6. 6University of California, Los Angeles, United States


Background Pulmonary arterial hypertension (PAH) is a leading cause of mortality in systemic sclerosis (SSc). Although medications have improved their prognosis, optimal therapy remains undefined. The goal of this study was to compare time to clinical worsening (TTCW) and survival based on initial oral PAH therapy.

Methods Using data from the PHAROS registry (a multicenter prospective observational study enrolling SSc patients with incident pulmonary hypertension), patients with group I PAH, 6 months of initial therapy with either an endothelin-receptor antagonist (ERA), phosphodiesterase-5 inhibitor (PDE5), or a combination of ERA/PDE5 were included. Patients treated initially with prostacyclins were excluded. The starting point for all analyses was the date of therapy initiation. Outcomes were survival and TTCW, defined as the first occurrence of death, PAH-related hospitalization, lung transplant, initiation of parenteral prostacyclin, or worsening symptoms.

Results Ninety-eight patients (initial ERA=24, initial PDE5=59, initial ERA/PDE5=15) were included; no significant differences in baseline variables existed. TTCW was significantly worse in patients initially started on ERA compared to PDE5 or ERA/PDE5 (p=0.0001). Baseline factors independently associated with shorter TTCW were initial ERA (HR 2.63, p=0.009), lower DLCO (HR 0.69 per 10% change, p=0.04), and higher PVR (HR 1.10 per Wood unit change, p=0.007). Three year survival was significantly worse in the initial ERA group (52.9%) compared to the PDE5 (91.5%) or ERA/PDE5 group (92.9%, p=0.004). The only baseline factor independently associated with risk for death in this cohort was initial ERA therapy (HR 4.55, p=0.004).

Conclusions Compared to PDE5 or combination ERA/PDE5, initial therapy with an ERA in SSc-PAH patients was associated with a significantly worse TTCW and survival, even after adjustment for commonly accepted prognostic factors. Although these findings may be the result of unmeasured imbalances between groups, it is plausible that known ERA side effects such as fluid retention may have led to clinical worsening. Limitations include data collection over non-uniform points in time and limited supplementary information as well as potential selection-bias in medication assignment. Further study into the optimal initial oral therapy in patients with SSc-PAH is needed.

Acknowledgements PHAROS is supported by an investigator initiated grant from Gilead Science.

Disclosure of Interest M. Lammi: None declared, L. A. Saketkoo Grant/research support from: ACR/EULAR Exchange Awardee; Gilead, S. Mathai Grant/research support from: National Heart and Blood Institute, Consultant for: Actelion Pharmaceuticals US, Bayer, R. Domsic: None declared, V. Steen Grant/research support from: Actelion Pharmaceuticals US Bayer CSL Berhing Intermune Roche Pharmaceuticals Sanofi-Aventis Pharmaceutical UCB United Therapeutics, D. Furst: None declared

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