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Survival and prognostic factors in pediatric patients with medulloblastoma treated at a national pediatric hospital in Peru: a retrospective cohort

Jose D. Flores-Sanchez Departments of Pediatric Neurosurgery and

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Daniela A. Perez-Chadid Faculty of Medicine, Universidad CES, Medellín, Antioquia, Colombia;

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Rosdali Y. Diaz-Coronado Department of Pediatric Oncology, Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru;

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Eddy Hernandez-Broncano Department of Pediatric Oncology, Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru;

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Carlos F. Ugas-Charcape Diagnostic Imaging, Instituto Nacional de Salud del Niño—San Borja, Lima, Peru;

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Alberto Ramirez Departments of Pediatric Neurosurgery and

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Augusto E. Racchumí-Vela Research and Technology Unit, Instituto Nacional de Salud del Niño—San Borja, Lima, Peru; and

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Frederick A. Boop 田纳西大学神经外科学系开云体育app官方网站下载入口e Health Sciences Center, Memphis, Tennessee

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Ivethe Preguntegui Departments of Pediatric Neurosurgery and

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OBJECTIVE

The objectives of this study were to determine the overall survival (OS) and event-free survival (EFS) rates of patients with medulloblastoma treated in a national pediatric hospital in Peru, as well as to identify demographic, clinical, imaging, postoperative, and histopathological characteristics and prognostic factors associated with OS and EFS.

开云体育世界杯赔率

The authors conducted a retrospective study analyzing information from the medical records of children with a diagnosis of medulloblastoma who underwent surgical treatment at the Instituto Nacional de Salud del Niño—San Borja, a public hospital in Lima, Peru, from 2015 to 2020. Clinical-epidemiological variables, degree of disease extension, risk stratification, extent of resection, postoperative complications, status of oncological treatment received, histological subtype, and neurological sequelae were taken into account. The Kaplan-Meier method and Cox regression analysis were used to estimate OS, EFS, and prognostic factors.

RESULTS

Of the 57 children evaluated with complete medical records, only 22 children (38.6%) underwent complete oncological treatment. OS was 37% (95% CI 0.25–0.55) at 48 months. EFS was 44% (95% CI 0.31–0.61) at 23 months. High-risk stratification—meaning patients with ≥ 1.5 cm2of residual postoperative tumor, those younger than 3 years, those with disseminated disease (HR 9.69, 95% CI 1.40–67.0, p = 0.02), and those who underwent subtotal resection (HR 3.78, 95% CI 1.09–13.2, p = 0.04)—was negatively associated with OS. Failure to receive complete oncological treatment was negatively associated with OS (HR 20.0, 95% CI 4.84–82.6, p < 0.001) and EFS (HR 7.82, 95% CI 2.47–24.7, p < 0.001).

CONCLUSIONS

操作系统和EFS medullob患者lastoma in the author’s milieu are below those reported in developed countries. Incomplete treatment and treatment abandonment in the authors’ cohort were also high compared with high-income country statistics. Failure to complete oncological treatment was the most important factor associated with poor prognosis, both in terms of OS and EFS. High-risk patients and subtotal resection were negatively associated with OS. Interventions are needed to promote the completion of adjuvant oncological therapy for medulloblastoma in the disadvantaged Peruvian population.

ABBREVIATIONS

CNS = central nervous system ; EFS = event-free survival ; LMIC = low- and middle-income country ; OS = overall survival ; PAHO = Pan-American Health Organization .
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