Kallen Michael E, Koka Rima, Singh Zeba N, Ning Yi, Kocoglu Mehmet H, Badros Ashraf Z, Niyongere Sandrine, Duong Vu H, Emadi Ashkan, Baer Maria R
Department of Pathology, University of Maryland School of Medicine, Baltimore, MD, United States.
Department of Medicine, Division of Hematology/Oncology, University of Maryland School of Medicine, Baltimore, MD, United States.
Leuk Res Rep. 2022 Nov 1;18:100358. doi: 10.1016/j.lrr.2022.100358. eCollection 2022.
New therapies for multiple myeloma have improved outcomes, but are associated with therapy-related hematologic malignancies. We report eight patients with therapy-related B-lymphoblastic leukemias (t-B-ALL) in the setting of therapy for multiple myeloma, which included lenalidomide maintenance. A subset of patients had pancytopenia and low-level marrow involvement by acute leukemia, an unusual finding in de novo B-ALL. One patient died of chemotherapy complications; the other seven responded. No patient died of B-ALL (median follow up of 1.0 years). Our series suggests that t-B-ALL is clonally unrelated to myeloma, presents with diverse cytogenetic abnormalities, and responds well to B-ALL therapy.
多发性骨髓瘤的新疗法改善了治疗效果,但与治疗相关的血液系统恶性肿瘤有关。我们报告了8例在多发性骨髓瘤治疗过程中发生治疗相关B淋巴细胞白血病(t-B-ALL)的患者,其中包括来那度胺维持治疗。一部分患者存在全血细胞减少和急性白血病引起的低水平骨髓受累,这在原发性B-ALL中是不寻常的发现。1例患者死于化疗并发症;其他7例有反应。无患者死于B-ALL(中位随访1.0年)。我们的系列病例表明,t-B-ALL与骨髓瘤克隆无关,具有多种细胞遗传学异常,且对B-ALL治疗反应良好。