Anderson Richard C E, Kennedy Benjamin, Yanes Candix L, Garvin James, Needle Michael, Canoll Peter, Feldstein Neil A, Bruce Jeffrey N
Departments of Neurosurgery, Columbia University, College of Physicians and Surgeons, New York, NY 10032, USA.
J Neurosurg Pediatr. 2013 Mar;11(3):289-95. doi: 10.3171/2012.10.PEDS12142. Epub 2012 Dec 14.
Convection-enhanced delivery (CED) for the treatment of malignant gliomas is a technique that can deliver chemotherapeutic agents directly into the tumor and the surrounding interstitium through sustained, low-grade positive-pressure infusion. This allows for high local concentrations of drug within the tumor while minimizing systemic levels that often lead to dose-limiting toxicity. Diffuse intrinsic pontine gliomas (DIPGs) are universally fatal childhood tumors for which there is currently no effective treatment. In this report the authors describe CED of the topoisomerase inhibitor topotecan for the treatment of DIPG in 2 children. As part of a pilot feasibility study, the authors treated 2 pediatric patients with DIPG. Stereotactic biopsy with frozen section confirmation of glial tumor was followed by placement of bilateral catheters for CED of topotecan during the same procedure. The first patient underwent CED 210 days after initial diagnosis, after radiation therapy and at the time of tumor recurrence, with a total dose of 0.403 mg in 6.04 ml over 100 hours. Her Karnofsky Performance Status (KPS) score was 60 before CED and 50 posttreatment. Serial MRI initially demonstrated a modest reduction in tumor size and edema, but the tumor progressed and the patient died 49 days after treatment. The second patient was treated 24 days after the initial diagnosis prior to radiation with a total dose of 0.284 mg in 5.30 ml over 100 hours. Her KPS score was 70 before CED and 50 posttreatment. Serial MRI similarly demonstrated an initial modest reduction in tumor size. The patient subsequently underwent fractionated radiation therapy, but the tumor progressed and she died 120 days after treatment. Topotecan delivered by prolonged CED into the brainstem in children with DIPG is technically feasible. In both patients, high infusion rates (> 0.12 ml/hr) and high infusion volumes (> 2.8 ml) resulted in new neurological deficits and reduction in the KPS score, but lower infusion rates (< 0.04 ml/hr) were well tolerated. While serial MRI showed moderate treatment effect, CED did not prolong survival in these 2 patients. More studies are needed to improve patient selection and determine the optimal flow rates for CED of chemotherapeutic agents into DIPG to maximize safety and efficacy. Clinical trial registration no.: NCT00324844.
对流增强递送(CED)用于治疗恶性胶质瘤是一种可通过持续的低级别正压输注将化疗药物直接递送至肿瘤及其周围间质的技术。这使得肿瘤内药物局部浓度较高,同时将常导致剂量限制性毒性的全身药物水平降至最低。弥漫性内生脑桥胶质瘤(DIPG)是普遍致命的儿童肿瘤,目前尚无有效治疗方法。在本报告中,作者描述了拓扑异构酶抑制剂拓扑替康通过CED治疗2例儿童DIPG的情况。作为一项初步可行性研究的一部分,作者治疗了2例患有DIPG的儿科患者。在同一手术过程中,经立体定向活检并通过冰冻切片证实为胶质瘤后,放置双侧导管进行拓扑替康的CED。首例患者在初始诊断210天后、放疗后及肿瘤复发时接受CED,在100小时内于6.04 ml中注入总剂量0.403 mg。她的卡氏功能状态(KPS)评分在CED前为60分,治疗后为50分。系列MRI最初显示肿瘤大小和水肿有适度减小,但肿瘤进展,患者在治疗后49天死亡。第二例患者在初始诊断24天后、放疗前接受治疗,在100小时内于5.30 ml中注入总剂量0.284 mg。她的KPS评分在CED前为70分,治疗后为50分。系列MRI同样显示肿瘤大小最初有适度减小。该患者随后接受了分次放疗,但肿瘤进展,她在治疗后120天死亡。通过延长CED将拓扑替康递送至患有DIPG的儿童脑干在技术上是可行的。在两名患者中,高输注速率(> 0.12 ml/小时)和高输注量(> 2.8 ml)导致了新的神经功能缺损和KPS评分降低,但较低的输注速率(< 0.04 ml/小时)耐受性良好。虽然系列MRI显示有中度治疗效果,但CED并未延长这2例患者的生存期。需要更多研究来改善患者选择,并确定将化疗药物通过CED递送至DIPG的最佳流速,以最大限度地提高安全性和疗效。临床试验注册号:NCT00324844。