A Favorable Outcome With CPX-351 Liposome (Vyxeos) in the Management of A Sporadic Monosomy 7 Myelodysplastic Syndrome Related Acute Myeloid Leukemia

M. Z. Mohamed Jiffry, Jonathan Vargas, M. Ahmed-khan, Teena Thomas, Jeltsina Sosa
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Abstract

Introduction: Although Acute Myeloid Leukemia (AML) has been associated with several environmental factors, in some patients the evolution to AML is preceded by myelodysplastic syndrome (MDS). We report a case of 63-year-old male who was diagnosed with sporadic monosomy 7 MDS/AML who achieved good response to treatment with CPX-351 (Vyxeos) induction chemotherapy. Case information: A 63-year-old male initially presented to the ED for further evaluation of pancytopenia that was discovered incidentally during a routine office visit. Further evaluation revealed his blast count was elevated with presence of Auer rods, myelocytes and basophilia. He was admitted for further work-up of pancytopenia with suspicion being for MDS/AML and bone marrow biopsy for flow cytometric evaluation of the bone marrow was strongly suggestive of acute myeloid leukemia, with morphology suggesting a predisposing MDS. Subsequent molecular cytogenetic [FISH] report confirmed -7/7q abnormality in 80% of nuclei with loss of 1 copy of chromosome 7. The following week, patient was initiated on CPX–351 [Vyxeos; daunorubicin and cytarabine liposome for injection]. Bone marrow biopsy following induction chemotherapy showed 11 to 12% of CD34 positive myeloid blasts with abnormal myeloid maturation, representing notable improvement with greater than 50% reduction in his blast count. Conclusion: Sporadic monosomy 7 MDS/AML that arises without evidence of germline genetic predisposition and in the absence of other predisposing medical conditions or treatments is an uncommon subset of AML. Vyxeos induction chemotherapy may be an excellent option in the management of sporadic monosomy 7 MDS/AML.
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CPX-351脂质体(Vyxeos)治疗散发性单体7骨髓增生异常综合征相关急性髓系白血病的有利结果
虽然急性髓性白血病(AML)与多种环境因素有关,但在一些患者中,AML的演变是由骨髓增生异常综合征(MDS)引起的。我们报告一例63岁男性被诊断为散发性单体7 MDS/AML,他对CPX-351 (Vyxeos)诱导化疗取得了良好的反应。病例信息:一名63岁男性,在例行就诊时偶然发现全血细胞减少症,最初到急诊科进行进一步评估。进一步的评估显示他的细胞计数升高,存在奥尔棒、髓细胞和嗜碱性细胞。他进一步接受全血细胞减少检查,怀疑是MDS/AML,骨髓活检进行骨髓流式细胞术评估强烈提示急性髓性白血病,形态学提示易感MDS。随后的分子细胞遗传学[FISH]报告证实-7/7q异常在80%的细胞核中,7号染色体1拷贝丢失。接下来的一周,患者开始使用CPX-351 [Vyxeos;注射用柔红霉素和阿糖胞苷脂质体]。诱导化疗后的骨髓活检显示,11 - 12%的CD34阳性骨髓母细胞有异常的骨髓成熟,表现出明显的改善,母细胞计数减少了50%以上。结论:散发性单体7 MDS/AML在没有生殖系遗传易感性的证据和没有其他易感医学条件或治疗的情况下出现,是AML的一个罕见亚群。Vyxeos诱导化疗可能是治疗散发性单体7 MDS/AML的一个很好的选择。
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