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Results from a post hoc analysis of the phase IIIb JUMP (NCT01493414) trial evaluating ruxolitinib ± anemia-supporting therapies in patients with myelofibrosis (MF) and anemia (hemoglobin [Hb] <12.0 g/dL) were published in Hematology by Vachhani et al. The analysis set included patients who initiated erythropoiesis-stimulating agent (ESA) or danazol <3 months post-enrollment and maintained ESA/danazol for ≥3 months (Hb <12.0 g/dL, n = 101; Hb <10.0 g/dL, n = 52); patients who had Hb <12.0 g/dL but did not initiate anemia-supporting medications within 3 months acted as an unmatched comparator (n = 1,242). Patients were evaluated for spleen length response (SLR), defined as ≥50% reduction from baseline in palpable spleen length, at Weeks 12 and 24, and for Functional Assessment of Cancer Therapy–Lymphoma (FACT-Lym) total score (TS) symptom response, defined as an ≥6.5-point increase from baseline, at Week 24.
Key data: Mean total daily ruxolitinib dose was maintained at near or above 25 mg throughout the study in all subgroups. At Week 12, 41.6% of patients in the analysis set demonstrated an SLR, including 42.3% of patients in the Hb <10.0 g/dL subset, compared with 35.0% of patients who did not initiate anemia-supporting therapies. At Week 24, 36.6% of patients in the analysis set had an SLR, including 34.6% of patients in the Hb < 10.0g/dL subset, compared with 28.4% of patients who did not initiate anemia-supporting therapies and 31.5% of patients in the total JUMP population. At Week 24, a FACT-Lym TS symptom response was demonstrated by 25.7% of patients in the analysis set, including 23.1% of patients in the Hb <10.0 g/dL subset; similar rates were observed in patients who did not initiate anemia-supporting therapies (26.5%) and the overall JUMP population (26.9%). Hb levels dropped through Week 4 but recovered to baseline by Week 48.
Key learning: In this post hoc analysis of the JUMP trial, the addition of anemia-supporting therapies to ruxolitinib preserved spleen and symptom response rates in patients with MF and anemia.
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This content is accurate as of the date of publication and is not updated retrospectively. Please refer to the latest available evidence, guidelines, and relevant regulatory information when making clinical decisions.
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Among patients with myelofibrosis and isolated anemia at presentation, with no indication for treatment with a JAK inhibitor, how often do you use anemia-directed treatments (EMAs, ESAs, danazol, etc.) as monotherapy?