Department of Hematology, Osaka Saiseikai Nakatsu Hospital, 2-10-39, Shibata, Kita-Ku, Osaka, 530-0012, Japan.
Department of Hematology, Graduate School of Medicine, Osaka City University, 1-4-3, Asahi-Machi, Abeno-Ku, Osaka, 545-8585, Japan.
Int J Hematol. 2024 Jan;119(1):88-92. doi: 10.1007/s12185-023-03678-9. Epub 2023 Nov 27.
Myeloid/natural killer (NK) cell precursor acute leukemia (MNKPL) is a rare leukemia subtype that possibly originates from precursor NK cells. The disease has a poor prognosis, and information on its treatment is lacking. We herein report the first case of a 46-year-old woman with MNKPL who was refractory to two lines of acute myeloid leukemia (AML)-type intensive chemotherapy but was successfully treated with venetoclax and azacytidine (VEN/AZA). She was diagnosed with MNKPL based on the conformations of immature lymphoblastoid morphology without myeloperoxidase reactivity that showed a CD7/CD33/CD34/CD56/HLA-DR positive phenotype and extramedullary regions. The disease was refractory to induction therapy with daunorubicin and cytarabine (DNR/Ara-C) and to reinduction therapy with mitoxantrone, etoposide, and cytarabine (MEC). After two lines of induction chemotherapy, massive pericardial and pleural effusion was found, and was suspected to be extramedullary lesions. The patient developed cardiac tamponade and required pericardiocentesis. Thus, VEN/AZA was administered as third-line therapy. After two cycles of VEN/AZA, the pericardial and pleural effusion disappeared, and complete remission was achieved. The patient received post-transplant cyclophosphamide-based haploidentical transplantation and has stayed relapse-free as of her last follow-up examination 2 years after diagnosis.
髓系/自然杀伤 (NK) 细胞前体急性白血病 (MNKPL) 是一种罕见的白血病亚型,可能起源于前体 NK 细胞。该疾病预后较差,且缺乏相关治疗信息。我们在此报告首例 46 岁女性 MNKPL 病例,该患者对两线急性髓系白血病 (AML) 强化化疗均耐药,但接受 venetoclax 和 azacytidine (VEN/AZA) 治疗后获得成功。根据不成熟淋巴母细胞样形态无髓过氧化物酶反应的特征,该患者被诊断为 MNKPL,表现为 CD7/CD33/CD34/CD56/HLA-DR 阳性表型和骨髓外区域。该疾病对柔红霉素和阿糖胞苷 (DNR/Ara-C) 诱导治疗以及米托蒽醌、依托泊苷和阿糖胞苷 (MEC) 再诱导治疗均耐药。在两线诱导化疗后,发现大量的心包和胸腔积液,疑似骨髓外病变。患者发生心脏压塞,需要进行心包穿刺。因此,给予三线治疗 VEN/AZA。在两个周期的 VEN/AZA 治疗后,心包和胸腔积液消失,达到完全缓解。患者接受了基于环磷酰胺的移植后半相合移植,在诊断后 2 年的最后一次随访检查时无疾病复发。