Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2021 May;21(5):338-344. doi: 10.1016/j.clml.2020.12.025. Epub 2021 Jan 12.
Acquisition of additional cytogenetic abnormalities (ACAs) in addition to Philadelphia chromosome is frequently observed in patients with chronic myeloid leukemia (CML) in advanced phase. The presence of core binding factor (CBF) translocations determines the diagnosis of acute myeloid leukemia regardless of blast percentage, and CBF rearrangements are rarely identified as ACAs.
A retrospective chart review of patients with CML who had CBF rearrangement, t(8;21) or inv(16), in Philadelphia chromosome-positive clones was conducted. Additional cases of CML with CBF rearrangements were identified through literature review.
Between August 1997 and December 2014, we identified 11 patients who had Philadelphia chromosome and CBF rearrangement in the same clones: 1 (9%) with t(8;21) and 10 (91%) with inv(16). Nine (82%) patients were in blast phase, and 2 (18%) in second chronic phase. Four (36%) patients received tyrosine kinase inhibitor monotherapy, 2 (18%) received tyrosine kinase inhibitor and chemotherapy, and 5 (45%) received chemotherapy only. Three (27%) patients achieved complete remission with incomplete count recovery, and 4 (36%) had no response after the initial therapy. Three (27%) patients underwent allogeneic stem cell transplantation. The median event-free survival and overall survival for the 11 patients were 2 months and 6 months, respectively. Literature review identified 14 patients with CML with CBF rearrangement with a median overall survival of 14 months.
Acquisition of CBF rearrangement in addition to Philadelphia chromosome is a rare phenomenon associated with poor prognosis. CBF rearrangements as ACAs in patients with CML can be considered high-risk features.
在慢性髓性白血病(CML)的晚期患者中,除费城染色体外,常观察到获得额外细胞遗传学异常(ACAs)。核心结合因子(CBF)易位的存在无论原始细胞百分比如何,均可确定急性髓细胞白血病的诊断,而 CBF 重排很少被认为是 ACAs。
对 CML 患者进行了回顾性图表审查,这些患者的费城染色体阳性克隆中存在 CBF 重排、t(8;21)或 inv(16)。通过文献回顾确定了其他具有 CBF 重排的 CML 病例。
1997 年 8 月至 2014 年 12 月期间,我们发现 11 例患者的同一克隆中存在费城染色体和 CBF 重排:1 例(9%)为 t(8;21),10 例(91%)为 inv(16)。9 例(82%)患者处于原始细胞期,2 例(18%)处于第二慢性期。4 例(36%)患者接受酪氨酸激酶抑制剂单药治疗,2 例(18%)接受酪氨酸激酶抑制剂联合化疗,5 例(45%)仅接受化疗。3 例(27%)患者达到不完全缓解的完全缓解,4 例(36%)在初始治疗后无反应。3 例(27%)患者接受了同种异体干细胞移植。11 例患者的中位无事件生存和总生存时间分别为 2 个月和 6 个月。文献回顾确定了 14 例具有 CBF 重排的 CML 患者,中位总生存时间为 14 个月。
除费城染色体外,获得 CBF 重排是一种罕见的现象,预后不良。在 CML 患者中,CBF 重排作为 ACAs 可被视为高危特征。