Department of Medical Oncology, Tata Memorial Center, Mumbai, Maharashtra, India.
Homi Bhabha National Institute, Mumbai, Maharashtra, India.
Cytometry B Clin Cytom. 2021 May;100(3):345-351. doi: 10.1002/cyto.b.21958. Epub 2020 Oct 8.
Inconclusive knowledge persists regarding the course of chronic myeloid leukemia-chronic phase (CML-CP) patients with detectable abnormal blasts by flow-cytometry at diagnosis. The 2016 WHO classification is not specific regarding sub-classification of CML with <10% abnormal B-lymphoid blasts (ABLB), and suggests these patients often show rapid progression. We report the clinical course of pediatric CML-CP patients who had detectable abnormal blasts by flow-cytometry at baseline.
Retrospective audit of all pediatric CML patients between January 2013 and December 2017 were included. Their clinical presentation, demographic profile, and treatment outcomes were extracted from electronic medical records. Some of these patients got flow-cytometry done by default, though it was not a routine part of diagnostic CML marrow studies.
Amongst 65 pediatric CML patients, flow-cytometry at initial diagnosis was available in 15 (CP-12; AP-3). Of the 12 CML-CP patients, 10 (83%) had abnormal flow-cytometric findings-5 (50%) with mixed lineage blasts (4-B/Myeloid, 1-B/T/Myeloid), and myeloid lineage blasts in the remaining 5 (50%). At a median follow-up of 26 months (range: 9-34 months), 3/5 patients with ABLB at diagnosis progressed to frank blast crisis (2 B-cell; 1 Mixed lineage). None among the five patients with diagnostic myeloid-alone aberrant blasts progressed to blast crisis. Imatinib resistant mutation was also found in 3/5 (60%) CML-CP patients with these ABLB at baseline.
Although a retrospective study with limited sample size, presence of ABLB detected on flow-cytometry in CML-CP patients, had a noticeable early conversion to CML-BC in our cohort. Incorporation of flow-cytometry in diagnostic work-up can provide useful insight regarding the behavior of pediatric CML-CP patients and guide therapy.
在诊断时通过流式细胞术检测到异常原始细胞的慢性髓性白血病慢性期(CML-CP)患者的病程仍存在不确定的知识。2016 年世界卫生组织分类对于异常 B 淋巴细胞原始细胞(ABLB)<10%的 CML 亚类没有具体分类,并且表明这些患者通常表现为快速进展。我们报告了基线时通过流式细胞术检测到异常原始细胞的儿科 CML-CP 患者的临床病程。
回顾性审核了 2013 年 1 月至 2017 年 12 月期间所有儿科 CML 患者。从电子病历中提取他们的临床表现、人口统计学特征和治疗结果。其中一些患者是默认进行流式细胞术检测的,尽管这不是诊断性 CML 骨髓研究的常规部分。
在 65 名儿科 CML 患者中,有 15 名(CP-12;AP-3)在初始诊断时进行了流式细胞术检测。在 12 名 CML-CP 患者中,有 10 名(83%)有异常的流式细胞术发现-5 名(50%)有混合谱系原始细胞(4-B/髓系,1-B/T/髓系),其余 5 名(50%)为髓系原始细胞。在中位随访 26 个月(范围:9-34 个月)时,诊断时具有 ABLB 的 3/5 名患者进展为明显的急变期(2 名 B 细胞;1 名混合谱系)。在这 5 名具有诊断性髓系异常原始细胞的患者中,均未进展为急变期。在基线时具有这些 ABLB 的 5 名 CML-CP 患者中有 3 名(60%)发现伊马替尼耐药突变。
尽管这是一项回顾性研究,样本量有限,但我们的队列中,在 CML-CP 患者中通过流式细胞术检测到的 ABLB 确实存在早期明显转化为 CML-BC。在诊断性工作中加入流式细胞术可以为儿科 CML-CP 患者的行为提供有用的见解,并指导治疗。