长期来那度胺治疗后伴有BCR:: abl1样特征的b淋巴母细胞白血病。

Juli-Anne Gardner, Julian Sprague, Patricia T Greipp, Joanna L Conant
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引用次数: 0

摘要

来那度胺是沙利度胺的衍生物,是一种免疫调节药物(IMiD),近20年来一直是多发性骨髓瘤(MM)和其他血液系统恶性肿瘤的标准治疗药物。这些药物在MM治疗中的成功提高了患者的生存率,因此,患者面临继发性原发性恶性肿瘤(SPM)的风险,其中一些是MM治疗的结果。MM患者患急性髓性白血病(AML)和卡波西肉瘤的风险增加。此外,使用IMiDs治疗还与骨髓增生异常肿瘤(MDS)、皮肤鳞状细胞癌以及较少见的急性淋巴细胞白血病(ALL)的风险增加相关。我们报告了一例老年男性MM和多发性皮肤癌患者,他在维持来那度胺治疗10年后出现全血细胞减少症并被诊断为b淋巴母细胞白血病(B-ALL)。
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B-Lymphoblastic Leukemia with BCR::ABL1-like Features After Long-term Lenalidomide Therapy.

Objectives: Lenalidomide, a derivative of thalidomide, is a type of immunomodulatory drug (IMiD) that has been standard therapy for multiple myeloma (MM) and other hematologic malignancies for almost two decades. The success of these drugs in MM has contributed to increased survival of patients and, as a result, patients are at risk for a secondary primary malignancy (SPM), some of which occur as a result of treatment for MM. MM patients have an increased risk for acute myeloid leukemia (AML) and Kaposi sarcoma. In addition, treatment with IMiDs is also associated with an increased risk for myelodysplastic neoplasms (MDS), squamous cell carcinoma of the skin, and, less frequently, acute lymphoblastic leukemia (ALL). We present a case of an elderly male with MM and multiple subsequent skin cancers, who presented with pancytopenia and was diagnosed with B-lymphoblastic leukemia (B-ALL) after 10 years of maintenance lenalidomide therapy.

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