| Literature DB >> 32700989 |
Zhining Chen1,2, Shimin Hu1, Sa A Wang1, Marina Konopleva3, Zhenya Tang1, Jie Xu1, Shaoying Li1, Gokce Toruner1, Beenu Thakral1, L Jeffrey Medeiros1, Guilin Tang1.
Abstract
Rare patients with chronic myeloid leukemia (CML) can present initially in lymphoblastic crisis (LBC) mimicking Ph + B-lymphoblastic leukemia (B-ALL). We retrospectively reviewed 275 adults who diagnosed initially as Ph + B-ALL and identified 28 patients with at least one of three features supporting the diagnosis of CML-LBC: 1) a large discrepancy between the blast count and Ph + clone; 2) Ph + clone persistent when B-ALL in remission; 3) BCR/ABL1 fusion detected in segmented cells. BCR-ABL1 fusions were p210 in 25 patients and p190 in 3 patients. In comparison to patients with Ph + B-ALL, patients with CML-LBC were older; had higher leukocyte and absolute neutrophil counts; higher immature myeloid cells in peripheral blood; lower blast counts; and inferior outcomes. In addition, we prospectively analyzed 26 patients with Ph + B-lymphoblastic leukemia and identified 8 patients with features more consistent with CML-LBC. These findings highlight the importance of distinguishing CML-LBC from de novo Ph + B-ALL.Entities:
Keywords: B-lymphoblastic leukemia; Chronic myeloid leukemia; Philadelphia chromosome; lymphoblastic crisis
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Year: 2020 PMID: 32700989 DOI: 10.1080/10428194.2020.1795160
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022