Tremblay Douglas, Rippel Noa, Feld Jonathan, El Jamal Siraj M, Mascarenhas John
Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Oncologist. 2021 May;26(5):406-421. doi: 10.1002/onco.13769. Epub 2021 Apr 21.
Chronic myelomonocytic leukemia (CMML) is a hematologic malignancy characterized by absolute monocytosis, one or more lineage dysplasia, and proliferative features including myeloid hyperplasia, splenomegaly, and constitutional symptoms. Because of vast clinical heterogeneity in presentation and course, risk stratification is used for a risk-adapted treatment strategy. Numerous prognostic scoring systems exist, some of which incorporate mutational information. Treatment ranges from observation to allogeneic hematopoietic stem cell transplantation. Therapies include hydroxyurea for cytoreduction, hypomethylating agents, and the JAK1/2 inhibitor ruxolitinib to address splenomegaly and constitutional symptoms. Recently, oral decitabine with cedazuridine was approved and represents a convenient treatment option for CMML patients. Although novel therapeutics are in development for CMML, further work is needed to elucidate possible targets unique to the CMML clone. In this review, we will detail the pathophysiology, risk stratification, available treatment modalities, and novel therapies for CMML, and propose a modern treatment algorithm. IMPLICATIONS FOR PRACTICE: Chronic myelomonocytic leukemia (CMML) is a clinically heterogenous disease, which poses significant management challenges. The diagnosis of CMML requires bone marrow biopsy and aspirate with thorough evaluation. Risk stratification and symptom assessment are essential to designing an effective treatment plan, which may include hypomethylating agents (HMAs) in intermediate or high-risk patients. The recently approved oral decitabine/cedazuridine provides a convenient alternative to parenteral HMAs. Ruxolitinib may be effective in ameliorating proliferative symptoms and splenomegaly. Allogeneic stem cell transplantation remains the only treatment with curative potential; however, novel therapies are in clinical development which may significantly alter the therapeutic landscape of CMML.
慢性粒单核细胞白血病(CMML)是一种血液系统恶性肿瘤,其特征为绝对单核细胞增多、一种或多种谱系发育异常以及增殖性特征,包括髓样增生、脾肿大和全身症状。由于临床表现和病程存在巨大的临床异质性,风险分层用于制定风险适应性治疗策略。存在多种预后评分系统,其中一些纳入了突变信息。治疗范围从观察到异基因造血干细胞移植。治疗方法包括使用羟基脲进行细胞减灭、使用去甲基化药物,以及使用JAK1/2抑制剂鲁索替尼来解决脾肿大和全身症状。最近,口服地西他滨联合西扎珠苷已获批准,这为CMML患者提供了一种便捷的治疗选择。尽管针对CMML的新型疗法正在研发中,但仍需要进一步开展工作以阐明CMML克隆特有的可能靶点。在本综述中,我们将详细阐述CMML的病理生理学、风险分层、可用的治疗方式和新型疗法,并提出一种现代治疗算法。对实践的启示:慢性粒单核细胞白血病(CMML)是一种临床异质性疾病,带来了重大的管理挑战。CMML的诊断需要进行骨髓活检和抽吸,并进行全面评估。风险分层和症状评估对于设计有效的治疗方案至关重要,该方案可能包括对中高危患者使用去甲基化药物(HMAs)。最近批准的口服地西他滨/西扎珠苷为非肠道HMAs提供了一种便捷的替代方案。鲁索替尼可能有效改善增殖症状和脾肿大。异基因干细胞移植仍然是唯一具有治愈潜力的治疗方法;然而,新型疗法正在临床研发中,可能会显著改变CMML的治疗格局。