A Single Center Clinical Analysis of Children with High-risk Neuroblastoma
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Methods: This study enrolled patients with high-risk neuroblastoma between 2009 and 2014 in Department of Pediatric Oncology of Tianjin Medical University Cancer Institute and Hospital. The clinical characteristics of patients were illustrated and surgery extent was evaluated by the impact on survival rate.
Results: The 3-year overall survival (OS) and progression-free survival (PFS) were 56.2% and 50.5%, respectively. LDH (P<0.001), bone marrow metastasis at time of diagnosis (P=0.001), bone marrow negative after neoadjuvant chemotherapy (P<0.001), radiotherapy (P<0.001) were significant predictors of OS and PFS. And surgery extent had no impact on the enhancement of high-risk neuroblastoma patients in short time.
Conclusions: This study showed no substantial survival benefit in patients with high-risk NB undergoing gross total tumor resection. Multidisciplinary intensive treatment was essential, especially for patients received subtotal tumor resection. Longer term follow-up is needed to survey complications in surviving patients who received intensive chemotherapy and radiotherapy.
Laura B, Radu B, Patricia C, Andreea M Children (Basel). 2022; 9(11).
PMID: 36360435 PMC: 9688519. DOI: 10.3390/children9111707.
[Clinical efficacy of combined therapy in children with stage 4 neuroblastoma].
Liang W, Ye X, Zhong G, Chen J, Dai K, Cheuk K Zhongguo Dang Dai Er Ke Za Zhi. 2022; 24(7):759-764.
PMID: 35894190 PMC: 9336616. DOI: 10.7499/j.issn.1008-8830.2203049.
The Significance of Histopathologic Assessment in Bone Marrow Disease in Neuroblastoma.
Ekmekci S, Ince D, Olgun N, Ozer E Turk Patoloji Derg. 2021; 38(2):99-105.
PMID: 34558657 PMC: 9999680. DOI: 10.5146/tjpath.2021.01556.
Advances in the Surgical Treatment of Neuroblastoma.
Luo Y, Cui X, Yang L, Zhang D, Wang J Chin Med J (Engl). 2018; 131(19):2332-2337.
PMID: 30246719 PMC: 6166470. DOI: 10.4103/0366-6999.241803.