Real-world clinical outcomes of patients with myelofibrosis treated with ruxolitinib: a medical record review

Future Oncol. 2022 Jun;18(18):2217-2231. doi: 10.2217/fon-2021-1358. Epub 2022 Apr 7.

Abstract

Aim: To assess real-world ruxolitinib treatment patterns and outcomes in patients diagnosed with primary or secondary myelofibrosis. Materials & methods: Patient medical records were reviewed in six countries. Results: Eligible patients (n = 469) had a mean age of 63.5 years, and most were male (66.5%) with primary myelofibrosis (78.5%). Median duration of ruxolitinib treatment was 13.1 months; 40% of patients initiated treatment at the recommended dose. The Kaplan-Meier estimate of median survival from ruxolitinib initiation was 44.4 months (95% CI, 38.8-50.2 months). Approximately one quarter (23%) of patients continued ruxolitinib after progression. Conclusion: These results suggest an unmet need for more effective treatments for patients with myelofibrosis who failed ruxolitinib.

Keywords: medical record review; myelofibrosis; real-world data; ruxolitinib; survival analysis.

MeSH terms

  • Female
  • Humans
  • Male
  • Medical Records
  • Middle Aged
  • Nitriles / therapeutic use
  • Primary Myelofibrosis* / drug therapy
  • Pyrazoles / therapeutic use
  • Pyrimidines / therapeutic use
  • Treatment Outcome

Substances

  • Nitriles
  • Pyrazoles
  • Pyrimidines
  • ruxolitinib

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