首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Management and outcomes of treating pediatric medulloblastoma: an eight years’ experience in an Iranian pediatric center
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Management and outcomes of treating pediatric medulloblastoma: an eight years’ experience in an Iranian pediatric center

机译:治疗儿科Medulloblastoma的管理和结果:伊朗儿科中心的八年经验

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Abstract Purpose The clinical management of pediatric medulloblastoma requires a multidisciplinary approach, which can be challenging, especially in low- and middle-income countries. The aim of this study was to identify current challenges and describe the treatment and outcomes of Iranian pediatric patients with medulloblastoma who were referred to our center in Tehran, Iran. Methods Our retrospective review included 126 patient records from April 2007 to May 2015. The records were analyzed for epidemiologic features, treatment modalities, overall survival, and progression-free survival. Data were analyzed using SPSS 22.0 software. Results Median age at diagnosis was 6?years (male:female ratio, 2.3:1). At the time of diagnosis, 7 patients were 2?years or younger, and 76 (60.3%) were categorized as having high-risk disease. Overall, 100 patients had gross or near-total surgical resection. Cerebral spinal fluid involvement was detected in 22.2% of the patients tested, and spinal involvement was detected in 25% of the patients who underwent spinal MRI. Metastasis stages at the time of diagnosis were as follows: M0: 48.4% patients, M1: 16.7%, M2: 5.5%, and M3: 21.4%. Median times of follow-up and progression-free survival were 16 and 12?months, respectively. Probability of 7-year overall survival and progression-free survival were 59 and 53.8%, respectively. Conclusions Results of the current retrospective study emphasize the need for implementing measures to improve outcome for our patients with medulloblastoma. Such measures include a multidisciplinary approach, unified national treatment guidelines, better disease and metastasis staging, twinning initiatives, and seeking a second opinion when needed.
机译:摘要目的儿科髓母细胞瘤的临床管理需要多学科方法,这可能具有挑战性,特别是在低收入和中等收入国家。本研究的目的是确定当前的挑战,并描述伊朗母细胞母细胞瘤的伊朗儿科患者的治疗和结果,伊朗在德黑兰的中心提交。方法采用我们的回顾综述包括从2007年4月到2015年5月的126名患者记录。分析了流行病学特征,治疗方式,整体生存和无进展生存的记录。使用SPSS 22.0软件进行分析数据。结果诊断中位年龄为6?年(男性:女性比例,2.3:1)。在诊断时,7例患者为2年或更小,76名(60.3%)分类为具有高危疾病。总体而言,100名患者具有粗略或近乎全面的手术切除。在22.2%的患者中检测到脑脊髓液中的参与,并在25%接受脊髓MRI的患者中检测到脊髓受累。诊断时的转移阶段如下:M0:48.4%患者,M1:16.7%,M2:5.5%和M3:21.4%。中位数的随访和无进展生存率分别为16和12个月。 7年整体存活和无进展生存率分别为59和53.8%。结论目前回顾性研究的结果强调了实施措施,以改善患有Medulloblastoma患者的结果。这些措施包括多学科方法,统一的国家治疗准则,更好的疾病和转移分期,孪生举措,并在需要时寻求第二种意见。

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