Dietrich Jörg, Marienhagen Jörg, Schalke Berthold, Bogdahn Ulrich, Schlachetzki Felix
Department of Biomedical Genetics, University of Rochester, Rochester, NY 14642-8609, USA.
Ann Pharmacother. 2004 Feb;38(2):242-6. doi: 10.1345/aph.1D106. Epub 2003 Dec 15.
To report a case of acute central nervous system (CNS) toxicity with multiple hemorrhages restricted to the corpus callosum associated with combination therapy of cisplatin, ifosfamide, and etoposide.
A 38-year-old white man with a testicular germ cell tumor received a cisplatin-based chemotherapy consisting of cisplatin 45 mg (20 mg/m2), etoposide 570 mg (250 mg/m2), and ifosfamide 4600 mg (2000 mg/m2) given on 5 consecutive days during each course. After the first course of chemotherapy, the patient appeared to be neuropsychologically impaired with episodes of decreased alertness and features of a depressive syndrome. He became severely diminished in mental function, orientation, and psychomotor activity after a second course of treatment. In addition, he showed transient urinary incontinence. Motor and sensory deficits could not be detected. Magnetic resonance imaging demonstrated multiple hemorrhages restricted to the corpus callosum. An objective causality assessment revealed that an adverse drug reaction was probable.
Neurotoxicity has been associated with the administration of various antineoplastic agents. In particular, cisplatin and ifosfamide can cause both acute and delayed CNS toxicity. While ifosfamide neurotoxicity has been predominantly associated with neuropsychological impairment without evidence of structural abnormalities in neuroimaging studies, cisplatin has been shown to cause cerebrovascular complications. Various pathophysiologic conditions may contribute to these complications including thrombosis secondary to vascular endothelial injury or thromboembolic events. To our knowledge, as of December 2, 2003, vascular lesions restricted to the corpus callosum have not been reported as a complication of cisplatin- or ifosfamide-based chemotherapy.
Clinicians should be aware of the potential neurovascular adverse effects of cisplatin-based protocols. This is especially true in patients with subtle neurologic or neuropsychological symptoms. Chemotherapy-induced neurotoxicity should be considered in the differential diagnosis.
报告1例急性中枢神经系统(CNS)毒性病例,该病例出现仅限于胼胝体的多处出血,与顺铂、异环磷酰胺和依托泊苷联合治疗有关。
一名38岁患有睾丸生殖细胞瘤的白人男性接受了以顺铂为基础的化疗,每个疗程连续5天给予顺铂45mg(20mg/m²)、依托泊苷570mg(250mg/m²)和异环磷酰胺4600mg(2000mg/m²)。在第一个化疗疗程后,患者出现神经心理受损,表现为警觉性下降和抑郁综合征特征。在第二个疗程治疗后,他的精神功能、定向力和精神运动活动严重减退。此外,他出现短暂性尿失禁。未检测到运动和感觉缺陷。磁共振成像显示多处出血仅限于胼胝体。客观因果关系评估显示可能为药物不良反应。
神经毒性与多种抗肿瘤药物的使用有关。特别是,顺铂和异环磷酰胺可引起急性和迟发性CNS毒性。虽然异环磷酰胺神经毒性主要与神经心理损害有关,神经影像学研究未显示结构异常证据,但顺铂已被证明可引起脑血管并发症。各种病理生理状况可能导致这些并发症,包括血管内皮损伤继发的血栓形成或血栓栓塞事件。据我们所知,截至2003年12月2日,仅限于胼胝体的血管病变尚未作为顺铂或异环磷酰胺为基础的化疗并发症报道。
临床医生应意识到以顺铂为基础方案的潜在神经血管不良反应。对于有轻微神经或神经心理症状的患者尤其如此。化疗引起的神经毒性应在鉴别诊断中予以考虑。