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. 2024 Feb 27:13:1326788.
doi: 10.3389/fonc.2023.1326788. eCollection 2023.

Primary central nervous system tumors survival in children in ten Colombian cities: a VIGICANCER report

Affiliations

Primary central nervous system tumors survival in children in ten Colombian cities: a VIGICANCER report

Oscar Ramirez et al. Front Oncol. .

Abstract

Purpose: Primary central nervous system (CNS) tumors are the second most common cancer in children and adolescents, leading to premature death and disability. Population-based survival estimates aid decision-making in cancer control, however data on survival for primary CNS tumors in Latin America is lacking. We describe survival rates for children with primary CNS tumors treated in ten Colombian cities.

Methods: We analyzed data from children and adolescents newly diagnosed with cancer between 2012 and 2021, participating in the Childhood Cancer Clinical Outcomes Surveillance System (VIGICANCER) in ten cities in Colombia. VIGICANCER collects information on clinical outcomes from twenty-seven pediatric oncology units and conducts active follow-up every three months. VIGICANCER does not register craniopharyngiomas; we excluded intracranial germ cell tumors for this report. We used the Kaplan-Meier method to estimate the overall survival probability, stratified by sociodemographic variables, topography, WHO grading, receipt of radiation therapy, and type of surgical resection. We analyzed the prognostic capacity of variables using multivariate proportional Cox's regression, stratified by city and year of diagnosis.

Results: During the study period, VIGICANCER included 989 primary CNS tumors in 879 children and 110 adolescents. The cohort median age was 9 years; 53% of patients were males, and 8% were Afro-descendants. Most common tumors were supratentorial astrocytomas (47%), astrocytic tumors (35%), medulloblastomas (20%), ependymomas (11%), and mixed and unspecified gliomas (10%). Five-year overall survival of the entire cohort was 54% (95% CI, 51-58); for supratentorial gliomas, WHO grade I was 77%, II was 62%, III-IV was 27%, respectively, and for medulloblastoma was 61%. The adjusted hazard rate ratio for patients with WHO grade III and IV, for those with subtotal resection, for brainstem location, and for those not receiving radiation therapy was 7.4 (95% CI, 4.7-11.8), 6.4 (95% CI, 4.2-9.8), 2.8 (95% 2.1-3.8), 2.0 (95% CI, 1.3-2.8) and 2.3 (95% CI, 1.7-3.0), respectively.

Conclusion: We found that half of Colombia's children and adolescents with primary CNS tumors survive five years, compared to 70% to 80% in high-income countries. In addition to tumor biology and location, gross total resection was crucial for improved survival in this cohort. Systematic monitoring of survival and its determinants provides empirical data for guiding cancer control policies.

Keywords: Latin America; central nervous system neoplasms; children; epidemiology; pediatrics; prognosis; survival; treatment outcome.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Flow chart of patients included in the analyses by topography.
Figure 2
Figure 2
Overall survival of patients with cerebral, cerebellar and brain stem tumors. Five-year OS for cerebral tumors was 52% (95% CI, 47-58), for cerebellar 64% (95% CI, 58-70) and for brain stem tumors of 19% (95% CI, 11-28).
Figure 3
Figure 3
Overall survival of patients with supratentorial gliomas by the WHO malignancy scale. Five-year OS for grade I was 77% (95% CI, 69-83), for grade II was 62% (95% CI, 44-75), grade III 17% (95% CI, 7-32) and grade IV 31% (95% CI, 22-41).
Figure 4
Figure 4
Overall survival of patients with medulloblastomas by risk classification. Five-year OS for the standard risk was 70% (95% CI, 60-78) and for high risk was 40% (95% CI, 26-54).

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