University of South Dakota Sanford School of Medicine, Sioux Falls, SD, USA.
Damascus University, Damascus, Syria.
BMC Neurol. 2022 Mar 19;22(1):107. doi: 10.1186/s12883-022-02576-7.
Longitudinal extensive transverse myelitis is a rare and potentially life-threatening complication of chemoradiation. Certain chemotherapy agents have been proposed to increased neurotoxicity with chemoradiation therapy. One such agent is durvalumab, a human IgG1 monoclonal antibody that blocks programmed death ligand 1, allowing T-cells to recognize and kill tumor cells. Durvalumab and other immune checkpoint inhibitors may also cause transverse myelitis without concomitant treatment with radiation. Durvalumab is a standard therapy for non-small cell lung carcinoma. Here we present a case of a 68-year-old male who presented after chemoradiation and durvalumab therapy with transverse myelitis extending outside the irradiation site.
A 68-year-old male presented to the emergency department with pain and weakness in his feet and hesitancy of urination. Medical history is significant for non-small cell lung cancer treated with chemoradiotherapy and consolidation therapy with durvalumab for one year. His last radiation treatment was 15 months prior, and his last infusion of durvalumab was 3 months prior. Exam revealed severe weakness of bilateral legs with absent vibration sensation. MRI showed central longitudinal extensive transverse myelitis extending from C4-T11. CSF studies showed 8 WBC with 63% lymphocyte predominance and a protein of 48. Oligoclonal bands and angiotensin-converting enzyme were negative. Serum Neuromyelitis Optica antibody (AQP4-IgG) and Myelin oligodendrocyte glycoprotein antibody (MOG-IgG) were negative. Infectious workup came back negative. The patient was treated with steroids and plasma exchange with mild improvement. Etiology remained unknown, but longitudinal extensive transverse myelitis following durvalumab chemoradiotherapy was thought to be the likely cause. He was discharged on a high-dose prednisone taper with outpatient follow-up. His condition worsened near the end of the steroid taper. High-dose prednisone and cyclophosphamide infusions were started with mild improvement and stabilization of the patient's condition. He transitioned to methotrexate after completion of six cyclophosphamide infusions. The patient expired due to complications from his cancer.
Longitudinal extensive transverse myelitis is a rare and potentially life-threatening complication of durvalumab therapy. As durvalumab has become a standard treatment for non-small cell lung cancer, it is important to be able to identify and treat side effects.
长节段横贯性脊髓炎是放化疗的一种罕见且潜在危及生命的并发症。某些化疗药物与放化疗联合应用可增加神经毒性。一种此类药物是度伐鲁单抗,这是一种人源 IgG1 单克隆抗体,可阻断程序性死亡配体 1,使 T 细胞能够识别并杀死肿瘤细胞。度伐鲁单抗和其他免疫检查点抑制剂也可能导致横贯性脊髓炎,而无需同时进行放射治疗。度伐鲁单抗是治疗非小细胞肺癌的标准疗法。在此,我们报告了 1 例 68 岁男性患者,在接受放化疗和度伐鲁单抗治疗后出现横贯性脊髓炎,病变范围超出照射部位。
一名 68 岁男性因脚部疼痛和无力以及排尿犹豫到急诊科就诊。该患者的既往病史包括非小细胞肺癌,接受了放化疗和巩固治疗(度伐鲁单抗治疗 1 年)。最后一次放疗是在 15 个月前,最后一次度伐鲁单抗输注是在 3 个月前。体格检查显示双侧下肢严重无力,振动觉缺失。MRI 显示 C4-T11 水平的中央长节段横贯性脊髓炎。CSF 研究显示白细胞 8 个,淋巴细胞占 63%,蛋白 48。寡克隆带和血管紧张素转换酶均为阴性。血清水通道蛋白 4 抗体(AQP4-IgG)和髓鞘少突胶质细胞糖蛋白抗体(MOG-IgG)均为阴性。感染性检查结果为阴性。患者接受了类固醇和血浆置换治疗,症状略有改善。病因仍不明,但考虑为度伐鲁单抗放化疗后长节段横贯性脊髓炎。患者出院时接受大剂量泼尼松逐渐减量治疗,并进行门诊随访。在激素逐渐减量接近尾声时,患者病情恶化。开始给予大剂量泼尼松和环磷酰胺输注,患者病情略有改善并稳定。在完成 6 次环磷酰胺输注后,患者转为甲氨蝶呤治疗。患者最终因癌症并发症去世。
长节段横贯性脊髓炎是度伐鲁单抗治疗的一种罕见且潜在危及生命的并发症。随着度伐鲁单抗成为非小细胞肺癌的标准治疗方法,识别和治疗其副作用非常重要。