pyrimidinones and Mediastinal-Neoplasms

Hematologic malignancies arising in the setting of established germ cell tumors have been previously described and have a dismal prognosis. Identification of targetable mutations and pathway dysregulation through massively parallel sequencing and functional assays provides new approaches to disease management.. Herein, we report the case of a 23-year-old male who was diagnosed with a mediastinal germ cell tumor and subsequent acute myeloid leukemia. A shared clonal origin was demonstrated through identification of identical NRAS and TP53 somatic mutations in both malignancies. The patient's leukemia was refractory to standard therapies with short interval relapse. Functional assays demonstrated the patient's blasts to be sensitive to the mitogen-activated protein kinase kinase (MEK) inhibitor trametinib, correlating with the activating NRAS mutation. The patient experienced a sustained partial remission while on trametinib therapy but ultimately suffered relapse of the germ cell tumor. The leukemic clone remained stable and sensitive to trametinib at that time.. This case highlights the potential power of combining genetic sequencing and in vitro functional assays with targeted therapies in the treatment of rare diseases.

Topics: Acute Disease; GTP Phosphohydrolases; High-Throughput Nucleotide Sequencing; Humans; Leukemia, Myeloid; Male; MAP Kinase Kinase 1; MAP Kinase Kinase 2; Mediastinal Neoplasms; Membrane Proteins; Neoplasm Recurrence, Local; Neoplasms, Germ Cell and Embryonal; Point Mutation; Protein Kinase Inhibitors; Pyridones; Pyrimidinones; Treatment Outcome; Tumor Suppressor Protein p53; Young Adult