Novel Janus-kinase (JAK) Inhibitors in Myelofibrosis.

Expert Opin Investig Drugs

Division of Hematology, Department of Internal Medicine, Cerrahpaşa Faculty of Medicine, Istanbul University-Cerrahpaşa, Istanbul, Turkey.

Published: November 2023

AI Article Synopsis

  • - JAK inhibitors (JAKis) are now a standard treatment for myelofibrosis, significantly reducing spleen size and improving patient symptoms, but challenges remain with treatment access and effectiveness.
  • - The review highlights investigational JAKis like jaktinib and momelotinib, assessing their outcomes from various clinical trials and preclinical studies.
  • - Expert opinions suggest that while some JAKis show promise in treating symptoms like anemia, more phase 3 studies are required to determine their long-term effectiveness and to create personalized treatment options.

Article Abstract

Introduction: JAK inhibitors (JAKis), used in the treatment of myelofibrosis, have entered standard treatment, providing significant improvements in spleen size and symptom burden. Although splenomegaly provides a reduction and some improvement in cytopenia, there is still a way to go. Novel JAKis are being investigated to overcome barriers to treatment access, such as therapeutic challenges, intolerance, and unresponsiveness.

Areas Covered: This review includes the current status of JAKi treatment for myelofibrosis, mainly focusing on investigational JAKis; jaktinib, lestaurtinib, itacitinib, gandotinib, BMS-911543, ilginatinib, TQ05105, and flonoltinib maleate. MEDLINE and clinicaltrials.gov were screened to identify all completed or active studies on this topic. The outcomes of the preclinical studies and clinical trials are presented and discussed for each drug.

Expert Opinion: In patients with myelofibrosis, momelotinib was effective in treating anemia, whereas jaktinib was effective in both anemia and Total Symptom Score (TSS). More phase 3 studies are needed to provide more precise evidence. The increasing variety of JAKis will allow for more personalized treatment options for myelofibrosis in the future. The potential impact on disease progression, molecular responses, and the duration of this response will become important parameters for future evaluations of these drugs.

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Source
http://dx.doi.org/10.1080/13543784.2023.2269078DOI Listing

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