PURPOSE: The REVEAL risk score (RRS) predicts 1-year survival in patients with pulmonary arterial hypertension; it also improved with riociguat in patients with inoperable or persistent/recurrent chronic thromboembolic pulmonary hypertension (CTEPH) in the Phase III CHEST-1 study, and predicted survival and clinical worsening-free survival (CWFS) in the long-term extension CHEST-2. RRS 2.0, an updated RRS, was developed based on modified point values, cut-offs, and variables. This post hoc analysis aimed to validate RRS 2.0 in the CHEST database (a population not derived from REVEAL), as done previously, and assess if the tool discriminates outcomes in a carefully selected and followed patient population. METHODS: RRS 2.0 was calculated for patients receiving riociguat up to 2.5 mg tid or placebo (pbo) at CHEST-1 baseline (BL) and Week 16, and CHEST-2 Week 12. Only patients enrolled in CHEST-2 were included. Patients were stratified by RRS 2.0 into low (≤7), average/moderately high (8-9), and high/very high (≥10) risk strata at BL and Week 16. Relationship between RRS 2.0 and survival and CWFS in CHEST-2 was examined by Kaplan-Meier and Cox proportional hazards analyses. RESULTS: At baseline, mean±SD RRS 2.0 was 7.1±2.7 in riociguat patients (n=155) and 6.9±2.6 in pbo patients (n=82). Risk status at BL was low in 131 patients (55%), average/moderately high in 59 (25%), and high/very high in 47 (20%). At CHEST-1 Week 16, riociguat improved RRS 2.0 by a least squares mean difference of -1.48 vs. pbo (95% CI -1.97 to -0.99; p<0.0001); risk status improved in 70% with riociguat and 39% with pbo patients (p<0.0001). At CHEST-2 Week 12, RRS 2.0 improved to 5.5±3.1 (n=152) and 6.1±3.1 (n=79) in riociguat and former pbo patients, respectively. In CHEST-2 (median [range] treatment duration 116 [2-232] weeks), Cox proportional hazards analyses showed RRS 2.0 at CHEST-1 BL and Week 16 was significantly associated with survival and CWFS (p<0.0001). Kaplan-Meier analyses showed significant differences in survival and CWFS between patients in the three risk strata at CHEST-1 BL and Week 16 (p<0.0001). CONCLUSION: Riociguat improved RRS 2.0 and risk strata in CHEST-1. RRS 2.0 predicted survival and CWFS over two years in CHEST-2. Thus, RRS 2.0 may be a useful tool to predict outcomes in patients with CTEPH. Further assessment of the discriminatory power of RRS 2.0 vs. the original RRS will be done.
|Original language||English (US)|
|Journal||The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation|
|State||Published - Apr 1 2020|
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine
- Cardiology and Cardiovascular Medicine