Real-world data for pediatric medulloblastoma: can we improve outcomes?

被引:0
作者
Paula Sedano
Carmen González-San Segundo
Lourdes De Ingunza
Pedro Cuesta-Álvaro
Marta Pérez-Somarriba
Francisco Diaz-Gutiérrez
Carmen Garrido Colino
Alvaro Lassaletta
机构
[1] Hospital General Universitario Gregorio Marañón,Radiation Oncology
[2] Complutense University of Madrid,Computing Services, Research Support
[3] Hospital Infantil Universitario Niño Jesús,Department of Pediatric Oncology
[4] Hospital General Universitario Gregorio Marañón,Pediatric Oncology
来源
European Journal of Pediatrics | 2021年 / 180卷
关键词
Medulloblastoma; Surgery; Radiotherapy; Survival; Treatment quality; Children;
D O I
暂无
中图分类号
学科分类号
摘要
Medulloblastoma (MB) is a malignant embryonal tumor that develops especially in childhood, with overall survival (OS) at 5 years of up to 70%. The objective of this study is to analyze treatment delivery variables in a retrospective cohort and evaluate the impact of these treatment quality parameters on survival. From 2000 to 2018, 40 pediatric patients with medulloblastoma, treated according to current international protocols, were retrospectively analyzed. Treatment delivery quality indicators were analyzed including the extent of surgery, radiotherapy (RT) parameters, and chemotherapy variables, related with time and dose-intensity deviations. With a median follow-up of 74 months (range, 6–195), OS at 5 years was 74 ± 7%, 81 ± 8% for standard-risk, and 55 ± 16% for high-risk patients (p = 0.090). Disease-free survival at 5 years was not significantly affected by extent of surgery (p = 0.428) and RT-related variables such as surgery-RT interval (p = 0.776) neither RT duration (p = 0.172) or maintenance chemotherapy compliance (p = 0.634). Multivariate analysis identified risk groups predictive of worse DFS (p = 0.032) and leptomeningeal dissemination associated with inferior OS (p = 0.029).
引用
收藏
页码:127 / 136
页数:9
相关论文
共 467 条
[1]  
RivasVilela S(2019)Incidence and survival of central nervous system tumors in childhood and adolescence in Girona (Spain) 1990–2013: national and international comparisons Clin Transl Oncol 21 1177-1185
[2]  
Rubio-Casadevall J(2017)Incidence and survival trends for medulloblastomas in the United States from 2001 to 2013 J Neuro-Oncol 135 433-441
[3]  
Fabrega-Ribas A(2007)The 2007 WHO classification of tumours of the central nervous system Acta Neuropathol 114 97-109
[4]  
Joly-Torta C(2017)The evolution of medulloblastoma therapy to personalized medicine F1000Res 6 490-1359
[5]  
Vilardell L(1969)An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas Radiology 93 1351-845
[6]  
Marcos-Gragera R(1999)Metastasis stage, adjuvant treatment, and residual tumor are prognostic factors for medulloblastoma in children: conclusions from the Children’s Cancer Group 921 randomized phase III study J Clin Oncol 17 832-831
[7]  
Khanna V(2016)Risk stratification of childhood medulloblastoma in the molecular era: the current consensus Acta Neuropathol 131 821-4208
[8]  
Achey RL(2006)Phase III study of craniospinal radiation therapy followed by adjuvant chemotherapy for newly diagnosed average-risk medulloblastoma J Clin Oncol 24 4202-787
[9]  
Ostrom QT(2008)Multi-institution prospective trial of reduced-dose craniospinal irradiation (23.4 Gy) followed by conformal posterior fossa (36 Gy) and primary site irradiation (55.8 Gy) and dose-intensive chemotherapy for average-risk medulloblastoma Int J Radiat Oncol Biol Phys 70 782-3193
[10]  
Block-Beach H(2012)Hyperfractionated versus conventional radiotherapy followed by chemotherapy in standard-risk medulloblastoma: results from the randomized multicenter HIT-SIOP PNET 4 Trial J Clin Oncol 30 3187-43