Efficacy of the Allosteric MEK Inhibitor Trametinib in Relapsed and Refractory Juvenile Myelomonocytic Leukemia: a Report from the Children’s Oncology Group

Author:

Stieglitz Elliot1ORCID,Lee Alex G.1ORCID,Angus Steven P.2ORCID,Davis Christopher2ORCID,Barkauskas Donald A.3ORCID,Hall David3ORCID,Kogan Scott C.4ORCID,Meyer Julia1ORCID,Rhodes Steven D.25ORCID,Tasian Sarah K.6ORCID,Xuei Xiaoling2ORCID,Shannon Kevin1ORCID,Loh Mignon L.7ORCID,Fox Elizabeth8ORCID,Weigel Brenda J.9ORCID

Affiliation:

1. Department of Pediatrics, Benioff Children’s Hospitals, University of California San Francisco, San Francisco, California. 1

2. Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana. 2

3. Children Oncology Group Operations and Data Center, Monrovia, California. 3

4. Department of Laboratory Medicine, University of California San Francisco, San Francisco, California. 4

5. Division of Pediatric Hematology-Oncology, Indiana University School of Medicine, Indianapolis, Indiana. 5

6. Children’s Hospital of Philadelphia, Division of Oncology and Center for Childhood Cancer Research and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania. 6

7. Ben Towne Center for Childhood Cancer Research, Seattle Children’s Research Institute and Department Pediatrics, Seattle Children’s Hospital, University of Washington, Seattle, Washington. 7

8. St. Jude Children’s Research Hospital, Memphis, Tennessee. 8

9. University of Minnesota, Minneapolis, Minnesota. 9

Abstract

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. See related commentary by Ben-Crentsil and Padron, p. 1574

Funder

National Cancer Institute

St. Baldrick’s Foundation

Alex’s Lemonade Stand Foundation for Childhood Cancer

Publisher

American Association for Cancer Research (AACR)

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