Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia
dc.contributor.author | Stieglitz, Elliot | |
dc.contributor.author | Lee, Alex G. | |
dc.contributor.author | Angus, Steven P. | |
dc.contributor.author | Davis, Christopher | |
dc.contributor.author | Barkauskas, Donald A. | |
dc.contributor.author | Hall, David | |
dc.contributor.author | Kogan, Scott C. | |
dc.contributor.author | Meyer, Julia | |
dc.contributor.author | Rhodes, Steven D. | |
dc.contributor.author | Tasian, Sarah K. | |
dc.contributor.author | Xuei, Xiaoling | |
dc.contributor.author | Shannon, Kevin | |
dc.contributor.author | Loh, Mignon L. | |
dc.contributor.author | Fox, Elizabeth | |
dc.contributor.author | Weigel, Brenda J. | |
dc.contributor.department | Pediatrics, School of Medicine | |
dc.date.accessioned | 2025-04-22T14:01:28Z | |
dc.date.available | 2025-04-22T14:01:28Z | |
dc.date.issued | 2024 | |
dc.description.abstract | Juvenile 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.version | Author's manuscript | |
dc.identifier.citation | Stieglitz 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.uri | https://hdl.handle.net/1805/47295 | |
dc.language.iso | en_US | |
dc.publisher | American Association for Cancer Research | |
dc.relation.isversionof | 10.1158/2159-8290.CD-23-1376 | |
dc.relation.journal | Cancer Discovery | |
dc.rights | Publisher Policy | |
dc.source | PMC | |
dc.subject | Protein kinase inhibitors | |
dc.subject | Pyridones | |
dc.subject | Pyrimidinones | |
dc.subject | Hematopoietic stem cell transplantation | |
dc.title | Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia | |
dc.type | Article |