Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia

dc.contributor.authorStieglitz, Elliot
dc.contributor.authorLee, Alex G.
dc.contributor.authorAngus, Steven P.
dc.contributor.authorDavis, Christopher
dc.contributor.authorBarkauskas, Donald A.
dc.contributor.authorHall, David
dc.contributor.authorKogan, Scott C.
dc.contributor.authorMeyer, Julia
dc.contributor.authorRhodes, Steven D.
dc.contributor.authorTasian, Sarah K.
dc.contributor.authorXuei, Xiaoling
dc.contributor.authorShannon, Kevin
dc.contributor.authorLoh, Mignon L.
dc.contributor.authorFox, Elizabeth
dc.contributor.authorWeigel, Brenda J.
dc.contributor.departmentPediatrics, School of Medicine
dc.date.accessioned2025-04-22T14:01:28Z
dc.date.available2025-04-22T14:01:28Z
dc.date.issued2024
dc.description.abstractJuvenile myelomonocytic leukemia (JMML) is a hematologic malignancy of young children caused by mutations that increase Ras signaling output. Hematopoietic stem cell transplantation (HSCT) is a potentially curative treatment, but patients with relapsed or refractory (advanced) disease have dismal outcomes. This phase II trial evaluated the safety and efficacy of trametinib, an oral MEK1/2 inhibitor, in patients with advanced JMML. Ten infants and children were enrolled, and the objective response rate was 50%. Four patients with refractory disease proceeded to HSCT after receiving trametinib. Three additional patients completed all 12 cycles permitted on study and continue to receive off-protocol trametinib without HSCT. The remaining three patients had progressive disease with two demonstrating molecular evolution by the end of cycle 2. Transcriptomic and proteomic analyses provided novel insights into the mechanisms of response and resistance to trametinib in JMML. ClinicalTrials.gov Identifier: NCT03190915. Significance: Trametinib was safe and effective in young children with relapsed or refractory JMML, a lethal disease with poor survival rates. Seven of 10 patients completed the maximum 12 cycles of therapy or used trametinib as a bridge to HSCT and are alive with a median follow-up of 24 months.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationStieglitz E, Lee AG, Angus SP, et al. Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia: a Report from the Children's Oncology Group. Cancer Discov. 2024;14(9):1590-1598. doi:10.1158/2159-8290.CD-23-1376
dc.identifier.urihttps://hdl.handle.net/1805/47295
dc.language.isoen_US
dc.publisherAmerican Association for Cancer Research
dc.relation.isversionof10.1158/2159-8290.CD-23-1376
dc.relation.journalCancer Discovery
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectProtein kinase inhibitors
dc.subjectPyridones
dc.subjectPyrimidinones
dc.subjectHematopoietic stem cell transplantation
dc.titleEfficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia
dc.typeArticle
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Stieglitz2024Efficacy-AAM.pdf
Size:
829.2 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.04 KB
Format:
Item-specific license agreed upon to submission
Description: