Evaluating pediatric spinal low-grade gliomas: a 30-year retrospective analysis
Autor: | Steven S. Carey, Anthony P. Y. Liu, Yahya Ghazwani, Ibrahim Qaddoumi, Amar Gajjar, Shengjie Wu, Sahaja Acharya, Zsila S. Sadighi, Thomas E. Merchant, Giles W. Robinson, Frederick A. Boop, Jason Chiang |
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Rok vydání: | 2019 |
Předmět: |
Male
Cancer Research medicine.medical_specialty Neurology Adolescent medicine.medical_treatment Scoliosis Disease-Free Survival Article 03 medical and health sciences 0302 clinical medicine Biopsy Adjuvant therapy Paralysis medicine Humans Spinal Cord Neoplasms Child Retrospective Studies Chemotherapy medicine.diagnostic_test business.industry Incidence (epidemiology) Infant Newborn Infant Glioma medicine.disease Surgery Treatment Outcome Oncology Tumor progression Child Preschool 030220 oncology & carcinogenesis Female Neurology (clinical) medicine.symptom business 030217 neurology & neurosurgery |
Zdroj: | J Neurooncol |
ISSN: | 1573-7373 0167-594X |
DOI: | 10.1007/s11060-019-03319-4 |
Popis: | PURPOSE: Most pediatric spinal tumors are low-grade gliomas (LGGs). Characterization of these tumors has been difficult given their heterogeneity and rare incidence. The objective was to characterize such tumors diagnosed at our institution. METHODS: Spinal tumors diagnosed in our pediatric patients between 1984 and 2014 were reviewed retrospectively. Demographics, presentation, pathology, imaging, management, and sequelae were examined. RESULTS: Forty patients had spinal LGG tumors, 24 (62%) of which were pilocytic astrocytomas. The most common initial presentations were pain (n=15), partial extremity paralysis (n=13), and ataxia (n=11), with the diagnosis frequently delayed by months (median=5.9 months, range=4 days-6.2 years). Twenty-nine patients had some tumor resection, and 8 required adjuvant therapy with chemotherapy (n=4) or radiation (n=4) post-resection. Ten other patients received only biopsy for histologic diagnosis, who were treated with chemotherapy (n=4) or radiation (n=5) post biopsy. Tumor progression was noted in 16 patients (2 after gross-total resection; 10, partial resection; and 4, biopsy). During the evaluation period, 3 patients died secondary to tumor progression. BRAF status could have shortened progression-free survival: patients with BRAFV600E mutations (n=3) all experienced progression within 10 months. Long-term sequelae of the disease/treatment were mostly residual neurologic deficits (paresthesia, paralysis), chemotherapy-induced hearing loss, and scoliosis. CONCLUSIONS: Spinal LGG is a rare entity with significant long-term effects. Although surgery is the most common initial treatment option, more in-depth analysis of molecular biomarkers may improve stratification and prognostication. |
Databáze: | OpenAIRE |
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