Stanková J, Kavan P, Krízová H, Hermanská E, Dosel P, Sázel M
Klinika dĕtské onkologie 2. LF UK a FNM, Praha.
Cas Lek Cesk. 2001 Jan 19;140(1):13-7.
Despite of improving diagnostics, development of new drugs and treatment strategies, patients with biologically unfavourable, advanced or relapsed neuroblastoma remain practically incurable. Treatment related toxicity, requirement for personnel and financial costs have became limiting. Tumor specific therapy represented by 131I-meta-iodobenzylguanidine (MIBG) administration could become an alternative improving the overall survival. In comparison with standard external radiotherapy the targeted therapy enables to achieve radiation 5 to 10 times higher with lower organ toxicity. Data published by European and American colleagues brought evidence of high efficacy of this method. It motivated us to set and develop the method at our department.
Retrospective analysis of therapeutic results and side effects of the administration of 131I-meta-iodobenzylguanidine in high-risk neuroblastoma patients cured at the Department of Pediatric Oncology in Prague since 1997 till 2000.
131I-meta-iodobenzylguanidine was fourteen times therapeutically administered in seven high-risk relapsed neuroblastoma patients. Four children received a single dose of 131I-meta-iodobenzylguanidine, three patients were treated repeatedly. The first dose represented 5.5 GBq, repeated dose 3.7 GBq, irrespective to the body weight. Each MIBG administration was followed by four days hyperbaric oxygen therapy. The treatment was well tolerated, acute and late side effects were not serious and only rarely reached grade 3 or 4 according to the International North American Children's Cancer Group Classification. Three of the seven children have survived with no evidence of the disease. Four children died of the disease progress.
131I-meta-iodobenzylguanidine treatment combined with hyperbaric oxygen therapy becomes a well-tolerated therapy for high-risk neuroblastoma patients non-responding to the conventional treatment. Though the 131I-meta-iodobenzylguanidine administration probably cannot cure these patients, the repeated administration can bring long lasting remission.
尽管诊断方法不断改进,新药和治疗策略不断研发,但生物学特性不良、晚期或复发的神经母细胞瘤患者实际上仍无法治愈。治疗相关的毒性、对人员的要求以及财务成本已成为限制因素。以施用131I-间碘苄胍(MIBG)为代表的肿瘤特异性疗法可能成为提高总体生存率的一种替代方法。与标准外照射放疗相比,靶向治疗能够在器官毒性较低的情况下使辐射剂量提高5至10倍。欧美同行发表的数据证明了该方法的高效性。这促使我们在本科室建立并开发该方法。
对1997年至2000年在布拉格儿科肿瘤学系治愈的高危神经母细胞瘤患者施用131I-间碘苄胍的治疗结果和副作用进行回顾性分析。
在7例高危复发神经母细胞瘤患者中对131I-间碘苄胍进行了14次治疗性给药。4名儿童接受了单次剂量的131I-间碘苄胍,3名患者接受了重复治疗。首剂为5.5GBq,重复剂量为3.7GBq,与体重无关。每次MIBG给药后进行4天的高压氧治疗。治疗耐受性良好,急性和晚期副作用不严重,根据国际北美儿童癌症组分类,仅很少达到3级或4级。7名儿童中有3名存活,无疾病证据。4名儿童死于疾病进展。
131I-间碘苄胍治疗联合高压氧治疗成为对传统治疗无反应的高危神经母细胞瘤患者耐受性良好的治疗方法。尽管施用131I-间碘苄胍可能无法治愈这些患者,但重复给药可带来长期缓解。