Targeted therapy in juvenile myelomonocytic leukemia: Where are we now?
Nele De VosMattias HofmansTim LammensBram De WildeNadine Van RoyBarbara De MoerloosePublished in: Pediatric blood & cancer (2022)
Juvenile myelomonocytic leukemia (JMML) is a rare and aggressive clonal neoplasm of early childhood, classified as an overlap myeloproliferative/myelodysplastic neoplasm by the World Health Organization. In 90% of the patients with JMML, typical initiating mutations in the canonical Ras pathway genes NF1, PTPN11, NRAS, KRAS, and CBL can be identified. Hematopoietic stem cell transplantation (HSCT) currently is the established standard of care in most patients, although long-term survival is still only 50-60%. Given the limited therapeutic options and the important morbidity and mortality associated with HSCT, new therapeutic approaches are urgently needed. Hyperactivation of the Ras pathway as disease mechanism in JMML lends itself to the use of targeted therapy. Targeted therapy could play an important role in the future treatment of patients with JMML. This review presents a comprehensive overview of targeted therapies already developed and evaluated in vitro and in vivo in patients with JMML.
Keyphrases
- acute myeloid leukemia
- wild type
- bone marrow
- end stage renal disease
- healthcare
- newly diagnosed
- ejection fraction
- chronic kidney disease
- low grade
- signaling pathway
- prognostic factors
- palliative care
- oxidative stress
- genome wide
- dna methylation
- quality improvement
- inflammatory response
- transcription factor
- patient reported
- genome wide identification