Paper Details 
Original Abstract of the Article :
Over the last decade, the Janus kinase1/2 (JAK1/2) inhibitor ruxolitinib has emerged as a cornerstone of myelofibrosis (MF) management. Ruxolitinib improves splenomegaly and symptoms regardless of driver mutation status, and confers a survival advantage in patients with intermediate-2/high risk MF. ...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/32297800

データ提供:米国国立医学図書館(NLM)

Navigating the Shifting Sands of Myelofibrosis Treatment

Myelofibrosis, a bone marrow disorder, is a challenging condition, like a shifting desert landscape that requires careful navigation. This study explores the management of myelofibrosis after ruxolitinib, a JAK1/2 inhibitor, has failed to provide a durable response. The authors discuss the challenges of treating myelofibrosis in the setting of ruxolitinib resistance, highlighting the limited treatment options and the need for further research to develop more effective therapies.

A Shifting Desert Landscape: Managing Myelofibrosis Resistance

The study highlights the need for novel therapeutic approaches to manage myelofibrosis in patients who have developed resistance to ruxolitinib. While new therapies, such as fedratinib, are being explored, further research is crucial to find effective treatment strategies for this challenging condition.

Finding a Sustainable Oasis: Evolving Treatments for Myelofibrosis

This research underscores the importance of ongoing research and development of new therapies for myelofibrosis. By exploring novel approaches and understanding the mechanisms of resistance, healthcare providers can provide more effective treatments for patients with this complex condition.

Dr. Camel's Conclusion

The desert of myelofibrosis treatment is vast and unforgiving, with the emergence of drug resistance posing a significant challenge. This study highlights the urgent need for new therapeutic strategies, reminding us that the quest for effective treatments must continue.

Date :
  1. Date Completed 2021-04-27
  2. Date Revised 2021-12-04
Further Info :

Pubmed ID

32297800

DOI: Digital Object Identifier

NIHMS1621231

Related Literature

SNS
PICO Info
in preparation
Languages

English

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