Clinical Feature and Genetic Alterations in Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia and Myeloid/NK Cell Acute Leukemia
Conclusions: Previously, it has been reported that outcome of MNKL is relatively good than MNKPL. MNKPL and MNKL children had a poor prognosis in our cohort even though most patients received HCT. We identified alteration of molecules involved in NOTCH signaling and RAS-MAPK pathways. In addition, mutations of several transcription factors such as WT1 were identified. The drugs targeting RAS pathway and epigenetic factors may have the potential to improve outcome. An international collaboration for clinical and cytogenetic research of MNKPL and MNKL is needed as they are complex and rare diseases.DisclosuresNo relevant conflicts of interest to declare.
Source: Blood - Category: Hematology Authors: Nishimura, A., Yokoyama, K., Yamagishi, C., Naruto, T., Morio, T., Kanai, A., Matsui, H., Higuchi, N., Takada, A., Okuno, H., Saito, S., Karakawa, S., Kobayashi, S., Sano, H., Koike, T., Hasegawa, D., Fujisaki, H., Hasegawa, D., Koike, K., Ogawa, A., Kino Tags: 618. Acute Lymphoblastic Leukemia: Biology, Cytogenetics, and Molecular Markers in Diagnosis and Prognosis: Poster II Source Type: research
More News: Acute Leukemia | Acute Lymphoblastic Leukemia | Acute Myeloid Leukemia | Biology | Cancer & Oncology | Chemotherapy | Children | Gastroschisis Repair | Genetics | Hematology | Hodgkin's Disease | Japan Health | Leukemia | Lymphoma | Molecular Biology | Non-Hodgkin's Lymphoma | Pediatrics | Rare Diseases | Study | Transplants