Abstract
Background: Pediatric gliomas comprise a clinically, histologically, and molecularly heterogeneous
group of central nervous system tumors. The survival of children with gliomas influenced
by histologic subtype, age, and extent of resection. Tumor grade emerged as the most
determinant of survival except in the young age groups. The aim of this study was
to evaluate the role of multidisciplinary therapeutic approach including surgery and
chemotherapy, and their impact on the outcome in pediatric patients with low-grade
glioma (LGG). Procedure: Study patients were prospectively enrolled onto the study. All patients were below
18-year-old, diagnosed as LGG between July 2007 and June 2012. Upfront surgical resection
was attempted in all tumors other than optic pathway sites. Systemic chemotherapy
was given according to CCG-A9952 protocol. Results: Total/near-total resection in 105/227 (46.3%) without adjuvant treatment, while 49/227
patients (21.5%) underwent subtotal tumor resection followed by chemotherapy for big
residual (n = 26). Follow-up only was indicated for asymptomatic/small residual (n = 23). The radiological diagnosis was set in 18/227 (7.9%) patients; 13/18 had optic
pathway glioma. The 3-year overall survival (OS) was 87.3% versus 65.5% event free
survival (EFS) for the whole study patients with a follow-up period of 1–5 years.
The OS and EFS for patients who did surgery with no adjuvant treatment (n = 128) were, respectively, 95.2% and 77.3% versus 87.4% and 65.1% for adjuvant chemotherapy
group (n = 99); (P = 0.015 and P = 0.016 for OS and EFS, respectively). Conclusion: Pediatric LGGs comprise a wide spectrum of pathological and anatomical entities that
carry a high rate of prolonged survival among children and adolescents. Surgical resection
is the mainstay of treatment in most of tumors. Combined chemotherapy can be an acceptable
alternative when surgery is not safely feasible.
Keywords
Chemotherapy - low-grade glioma - outcome - pediatric