高危神经母细胞瘤患者接受综合放疗后的局部控制和毒性结果:单个中心的 20 年经验。

Jeong Yun Jang, Jin-Hong Park, Yeon Joo Kim, Ho Joon Im, Kyung-Nam Koh, Hyery Kim, Sung Han Kang, Ha Un Kim, Seung Do Ahn
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引用次数: 0

摘要

背景:强化多模式治疗可提高高危神经母细胞瘤患者的生存率,而综合放疗有助于局部控制。我们研究了本院接受综合放疗患者的临床疗效:我们对牙山医疗中心 2001 年 3 月至 2021 年 3 月期间接受综合放疗的高危神经母细胞瘤患者的病历进行了回顾性分析。患者接受了多模式治疗,包括大剂量化疗、手术、干细胞移植和维持治疗。对原发部位和周围淋巴结进行放射治疗(中位数,21.0 Gy;范围,14-36):本研究共纳入 37 名患者,诊断时的中位年龄为 2.8 岁(范围为 1.3-10.0)。4例患者出现局部失败,5年无局部失败率为88.7%,中位随访时间为5.7年。5年无病生存率(DFS)和总生存率(OS)分别为59.1%和83.6%。单变量分析显示,神经元特异性烯醇化酶水平> 100 ng/mL的患者的无病生存期和总生存期明显较差(P = 0.036,0.048),而放疗前无残留疾病的患者的总生存期较好(P = 0.029)。此外,11q缺失或17q增益患者的DFS和OS分别较差(P = 0.021,0.011)。六名患者出现了一级急性毒性。晚期毒性在长期存活的儿童中得到证实,主要是甲状腺功能减退和性腺功能减退,通常<3级,可能与联合治疗有关。4名患者的晚期毒性≥3级,包括慢性肾病、生长激素异常、回肠炎、骨骺提前闭合和继发性肿瘤,通过住院或手术治疗痊愈:结论:对于高危神经母细胞瘤患者,对原发肿瘤部位进行综合放疗可取得良好的局部控制效果,且安全性可耐受。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Local control and toxicity outcomes following consolidative radiation therapy in patients with high-risk neuroblastoma: a 20-year experience at a single center.

Background: Intensive multimodal treatment can improve survival in patients with high-risk neuroblastoma, and consolidative radiation therapy has contributed to local control. We examined the clinical outcomes of patients who underwent consolidative radiation therapy at our institution.

Methods: We retrospectively reviewed the records of patients with high-risk neuroblastoma who underwent consolidative radiation therapy from March 2001 to March 2021 at Asan Medical Center. Patients underwent multimodal treatment including high-dose chemotherapy, surgery, stem cell transplantation, and maintenance therapy. Radiation (median, 21.0 Gy; range, 14-36) was administered to the primary site and surrounding lymph nodes.

Results: This study included 37 patients, and the median age at diagnosis was 2.8 years (range, 1.3-10.0). Four patients exhibited local failure, and 5-year free-from locoregional failure rate was 88.7%, with a median followup period of 5.7 years. The 5-year disease-free survival (DFS) and overall survival (OS) rates were 59.1% and 83.6%, respectively. Univariate analysis revealed that patients with neuron-specific enolase levels > 100 ng/mL had significantly worse DFS and OS (P = 0.036, 0.048), and patients with no residual disease before radiation therapy showed superior OS (P = 0.029). Furthermore, patients with 11q deletion or 17q gain exhibited poor DFS and OS, respectively (P = 0.021, 0.011). Six patients experienced grade 1 acute toxicity. Late toxicity was confirmed in children with long-term survival, predominantly hypothyroidism and hypogonadism, typically < grade 3, possibly attributed to combination treatment. Four patients experienced late toxicity ≥ grade 3 with chronic kidney disease, growth hormone abnormality, ileus, premature epiphyseal closure, and secondary tumor, and recovered by hospitalization or surgical treatment.

Conclusions: In patients with high-risk neuroblastoma, consolidative radiotherapy to the primary tumor site resulted in excellent local control and a tolerable safety profile.

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