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A matching-adjusted indirect comparison analysis compared OS in patients with MF who were previously treated with ruxolitinib and received momelotinib in a phase III trial (SIMPLIFY-1; NCT01969838; N = 432, SIMPLIFY-2; NCT02101268; N = 156, or MOMENTUM; NCT04173494; N = 195) or BAT from the retrospective RUX-MF study (n = 267).1 This analysis included two models, with model 2 having fewer matched characteristics to increase the ESS.1 Results were presented at the 66th ASH Annual Meeting and Exposition by Palandri.1 |
Key learnings |
In the matched analysis, OS was improved with momelotinib vs BAT in model 1 (ESS = 89; HR, 0.512; 95% CI, 0.358–0.732; p < 0.001) and in model 2 (ESS = 117; HR, 0.484; 95% CI, 0.347–0.675; p < 0.001). |
In the sensitivity analyses excluding ruxolitinib-randomized patients in SIMPLIFY-1 and momelotinib-randomized patients in MOMENTUM, respectively, the OS benefit of momelotinib vs BAT remained significant for both models. |
In the matched analysis for the anemic subgroup, OS favored momelotinib vs BAT (n = 174) in model 1 (ESS = 98; HR, 0.542; 95% CI, 0.387–0.759; p <0.001) and model 2 (ESS = 146; HR, 0.487; 95% CI, 0.360–0.660; p <0.001). |
Results from this analysis suggest that momelotinib improves OS vs BAT in patients with MF who were previously treated with ruxolitinib, both overall and in patients with anemia. |
Abbreviations: ASH, American Society of Hematology; BAT, best available therapy; CI, confidence interval; ESS, effective sample size; HR, hazard ratio; MF, myelofibrosis; OS, overall survival.
References
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