Study of Symptom Severity and Adherence to Therapy of Myelofibrosis Patients Treated with Ruxolitinib

Author:

Stoeva Vera1,Petrova Guenka2ORCID,Mitov Konstantin2,Tachkov Konstantin2

Affiliation:

1. Specialized Hospital for Active Treatment of Hematological Diseases, 1756 Sofia, Bulgaria

2. Faculty of Pharmacy, Medical University of Sofia, 1756 Sofia, Bulgaria

Abstract

We aimed to explore symptom severity and adherence to therapy for patients with myelofibrosis treated with ruxolitinib in Bulgaria. It is a prospective, non-interventional study performed at the specialized hospital for active treatment of hematological diseases in Sofia during 2022–2023. Date of diagnosis, demographic characteristics, clinical indicators, ruxolitinib dose, and other data points were collected. Clinical indicators were assessed at baseline, in the middle, and at the end of observation. Severity of symptoms was measured with MPN-SAF TSS and adherence to therapy with the Morisky 4 questionnaire six times during the observation. The mean age of diagnosis was 58.5 years, with the average duration of disease of 3 years. Patients’ laboratory results were within physiological ranges, with spleen size experiencing a constant decrease. The average value for the severity of the symptoms per MPN-SAF TSS results decreased significantly, indicating better disease control. The average adherence to therapy did not change and remained high at around 9 points, except for one patient. In conclusion the treatment of myelofibrosis patients with ruxolitinib decreased symptom severity and spleen size. Patients were adherent to the therapy over the observed period, but as treatment duration increases, the risk of adherence decreases.

Funder

Bulgarian National Science Fund

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

Reference23 articles.

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2. Mesa, R., Miller, C.B., Thyne, M., Mangan, J., Goldberger, S., Fazal, S., Ma, X., Wilson, W., Paranagama, D.C., and Dubinski, D.G. (2016). Myeloproliferative neoplasms (MPNs) have a significant impact on patients’ overall health and productivity: The MPN Landmark survey. BMC Cancer, 16.

3. United States Food and Drug Administration (2011). JAKAFI (Ruxolitinib) Label, FDA.

4. EMA (2023, May 24). European Public Assessment Report. Available online: https://www.ema.europa.eu/en/medicines/human/EPAR/inrebic.

5. EMA (2023, May 24). European Assessment Report. Available online: https://www.ema.europa.eu/en/documents/product-information/jakavi-epar-product-information_bg.pdf.

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