多发性骨髓瘤后继发性混合表型急性白血病首例报道。

American journal of blood research Pub Date : 2021-02-20 eCollection Date: 2021-01-01
Francesca Bacchiarri, Vincenzo Sammartano, Adele Santoni, Donatella Raspadori, Elisabetta Zappone, Marzia Defina, Sara Ciofini, Anna Sicuranza, Monica Bocchia, Alessandro Gozzetti
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引用次数: 0

摘要

近年来,由于新药物的使用,多发性骨髓瘤(MM)患者的预后有了显著改善。然而,一些药物,如烷基化药物美伐兰,可能与继发性恶性肿瘤的发生率增加有关。骨髓增生异常综合征和急性髓性白血病在文献中有报道,而急性淋巴细胞白血病很少报道。在这里,我们描述了一个独特的病例,自2015年以来,56岁女性MM患者在自体干细胞移植和来那度胺维持后完全缓解,2年后发展为混合表型急性白血病(MPAL)。该患者对淋巴细胞和髓性急性白血病治疗方案均难治,通过双特异性抗cd19 /抗cd3单克隆抗体blinatumumab和低甲基化剂azacytidine加BCL-2抑制剂venetoclax治疗,患者获得了完全缓解。然后她接受了来自hla相同的兄弟姐妹供体的造血干细胞移植,9个月后她仍然完全缓解。据我们所知,文献中没有描述MM自体移植后MPAL的病例。我们的患者接受blinatumomab和venetoclax治疗,并在同种异体移植后9个月完全缓解。MPAL发展的机制尚不完全清楚,治疗方法仍然缺乏。在这种情况下,blinatumomab, azacytidine和venetoclax在该患者中成功使用的组合可能为这种罕见患者的进一步研究提供了思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First reported case of secondary mixed phenotype acute leukemia after multiple myeloma.

In recent years the outcome of patients with multiple myeloma (MM) has significantly improved, due to new drugs. However, some agents, i.e. the alkylating drug melphalan, can be associated with an increased incidence of secondary malignancies. Myelodysplastic syndromes and acute myeloid leukemia are reported in the literature, and rarely acute lymphoblastic leukemia. Here we describe a unique case of a 56-years old female patient affected by MM since 2015 in complete remission after autologous stem cell transplant and in lenalidomide maintenance, who developed 2 years later mixed phenotype acute leukemia (MPAL). The patient, refractory to both lymphoblastic and myeloid acute leukemia regimens, achieved complete remission with bi-specific anti-CD19/anti-CD3 monoclonal antibody blinatumomab and with hypomethylating agent azacytidine plus the BCL-2 inhibitor venetoclax. She then underwent hematopoietic stem cell transplantation from HLA-identical sibling donor and she is still in complete remission after 9 months. To the best of our knowledge, there are no cases in the literature describing MPAL after autologous transplant for MM. Our patient was treated with blinatumomab and venetoclax and achieved complete remission 9 months from allogeneic transplant. The mechanism underlying the development of MPAL is not completely understood and therapies are still lacking. In this context the combination of blinatumomab, azacytidine and venetoclax successfully used in this patient may provide food for thought for further studies in this rare setting of patients.

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American journal of blood research
American journal of blood research MEDICINE, RESEARCH & EXPERIMENTAL-
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