Su Ying-Wen, Chang Ming-Chih, Chiang Ming-Fu, Hsieh Ruey-Kuen
Department of Hematology-Oncology, Mackay Memorial Hospital, Taiwan.
J Neurooncol. 2005 Feb;71(3):315-8. doi: 10.1007/s11060-004-2028-0.
In patients with recurrent malignant glioma, treatment-related myelodysplastic syndrome (t-MDS) and acute leukemia are rare adverse effects because the median survival after relapse is limited. We report a 44-year-old woman with t-MDS (refractory anemia with excess blasts) following treatment of recurrent anaplastic astrocytoma with temozolomide (TMZ). A cytogenetic study showed del (3)(q11.1). MDS was diagnosed 8.4 months after beginning TMZ. The disease rapidly evolved into acute leukemia within 1 month after the onset of MDS, and the patient died 1 month later during induction chemotherapy. The prognosis of t-MDS is generally poor. Considering the increasing use of TMZ, which is regarded as a drug with moderate toxicity, careful follow-up with routine blood testing is vital.
在复发性恶性胶质瘤患者中,治疗相关的骨髓增生异常综合征(t-MDS)和急性白血病是罕见的不良反应,因为复发后的中位生存期有限。我们报告一名44岁女性,在用替莫唑胺(TMZ)治疗复发性间变性星形细胞瘤后发生t-MDS(伴过多原始细胞的难治性贫血)。细胞遗传学研究显示del(3)(q11.1)。MDS在开始TMZ治疗8.4个月后被诊断出来。疾病在MDS发病后1个月内迅速演变为急性白血病,患者在诱导化疗期间1个月后死亡。t-MDS的预后通常较差。鉴于被视为具有中度毒性的TMZ使用日益增加,通过常规血液检测进行仔细随访至关重要。