Department of Neurology and Neurosurgery, Section of Hematology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Neuro Oncol. 2012 May;14(5):529-40. doi: 10.1093/neuonc/nos068. Epub 2012 Mar 29.
Treatment-related myelodysplastic syndrome (t-MDS) and treatment-related acute myelogenous leukemia (t-AML) represent rare secondary events in patients with primary tumors of the nervous system and predominantly affect those treated with alkylating agents or topoisomerase II inhibitors. Temozolomide has become the standard chemotherapeutic agent for malignant gliomas. The emergence of this alkylating agent with little acute toxicity or cumulative myelosuppression has led to off-label protracted chemotherapy for many patients with malignant and even low-grade infiltrative gliomas, raising concern for increased risk of t-MDS/t-AML in the few long-term survivors. On the basis of an extensive literature search, we provide a discussion of epidemiology, pathogenesis, clinical presentation, diagnosis, and therapy of these disorders. t-MDS/t-AML remain rare complications of chemotherapy in patients with primary brain tumors, and the vast majority of patients die of their primary neoplasm. Prospective randomized studies with long-term follow-up are required to accurately assess the risk of t-MDS/t-AML; however, unless survival in the most common gliomas substantially increases, t-MDS/t-AML incidence will likely remain low in this patient population.
治疗相关的骨髓增生异常综合征(t-MDS)和治疗相关的急性髓系白血病(t-AML)是原发性神经系统肿瘤患者中罕见的继发性事件,主要影响接受烷化剂或拓扑异构酶 II 抑制剂治疗的患者。替莫唑胺已成为恶性神经胶质瘤的标准化疗药物。这种具有低急性毒性或累积性骨髓抑制作用的烷化剂的出现,导致许多恶性甚至低级别浸润性神经胶质瘤患者的非适应证延长化疗,引起对少数长期幸存者中 t-MDS/t-AML 风险增加的担忧。基于广泛的文献检索,我们讨论了这些疾病的流行病学、发病机制、临床表现、诊断和治疗。t-MDS/t-AML 仍然是原发性脑肿瘤患者化疗的罕见并发症,绝大多数患者死于其原发性肿瘤。需要进行前瞻性随机研究并进行长期随访,以准确评估 t-MDS/t-AML 的风险;然而,除非最常见的神经胶质瘤的生存率显著提高,否则 t-MDS/t-AML 的发病率在该患者人群中可能仍然较低。