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Challenges in the management of childhood low-grade glioma in a developing country

Overview of attention for article published in Child's Nervous System, February 2018
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Title
Challenges in the management of childhood low-grade glioma in a developing country
Published in
Child's Nervous System, February 2018
DOI 10.1007/s00381-018-3729-6
Pubmed ID
Authors

Khalid Abdalla, Shaker Abdullah, Abeer Almehdar, Naglla Elimam, Mohammed Burhan Abrar, Wasil Jastaniah

Abstract

Treatment modality impacts outcome of childhood low-grade glioma (LGG). Optimizing management in developing countries can be challenging. This study evaluates the clinical characteristics, treatment, and factors influencing outcome of childhood LGG in Saudi Arabia. This study retrospectively evaluated 59 children consecutively diagnosed with LGG between January 2001 and June 2016. Median age at diagnosis was 6.0 years. Pilocytic astrocytoma represented 64.9% of cases. The anatomic site was cerebellar in 23.7%, cerebral in 18.6%, hypothalamic-optic pathway in 33.9%, and midline in 23.7%. The 5-year overall survival (OS) and progression-free survival (PFS) were 90.6 ± 4.7 and 54.3 ± 8.4%, respectively. Initial treatment was observation in 28.8%, surgery alone in 35.6%, chemotherapy in 13.6%, radiotherapy in 5.1%, and combined in 16.9% of cases. The corresponding 5-year PFS was 56.3 ± 15.6, 53.3 ± 14.0, 22.9 ± 19.7, 33.3 ± 27.2, and 88.9 ± 10.5%, respectively (p = 0.006). Among the 61% who had surgical intervention (either alone or in combination with other therapies), 22% achieved complete resection with 5-year radiation/progression-free survival (RPFS) of 87.5 ± 11.7% compared to 27.6 ± 10.8% for subtotal resection/biopsy and 62.2 ± 17.0% for no surgery (p = 0.013). Adjuvant therapy for residual tumor improved survival with 5-year PFS of 66.7 ± 19.2% for chemotherapy and 100% for radiotherapy compared to 12.5 ± 11.4% for observation (p = 0.033). We identified variability in the outcomes of LGG. Fewer surgeries with lower rates of total resection were noted, compared to reports from international cooperative groups. The extent of resection was predictive of RPFS. Adjuvant therapy improved the outcome of patients with residual disease, resulting in PFS rates comparable to international data.

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Geographical breakdown

Country Count As %
Unknown 36 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 4 11%
Student > Postgraduate 4 11%
Student > Bachelor 3 8%
Other 2 6%
Student > Master 2 6%
Other 3 8%
Unknown 18 50%
Readers by discipline Count As %
Medicine and Dentistry 14 39%
Biochemistry, Genetics and Molecular Biology 1 3%
Neuroscience 1 3%
Social Sciences 1 3%
Unknown 19 53%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 06 February 2018.
All research outputs
#20,462,806
of 23,020,670 outputs
Outputs from Child's Nervous System
#1,815
of 2,802 outputs
Outputs of similar age
#377,032
of 439,370 outputs
Outputs of similar age from Child's Nervous System
#61
of 68 outputs
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We're also able to compare this research output to 68 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.