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                  <text>2023 Special Edition 3 - Oncology List</text>
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              <text>2023 SE3 - Oncology</text>
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              <text>&lt;a href="http://doi.org/10.1002/pbc.30115" target="_blank" rel="noreferrer noopener"&gt; http://doi.org/10.1002/pbc.30115&lt;/a&gt;</text>
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                <text>The impact of clinical trial enrollment on specialty palliative care utilization in pediatric patients with high-grade gliomas</text>
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                <text>Pediatric Blood and Cancer</text>
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                <text>2023</text>
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                <text>Humans; Child; palliative care; Palliative Care; Disease Progression; Palliative Care; Clinical Trials as Topic; clinical trial; Glioma; Glioma/therapy/pathology; high-grade glioma; pediatric brain tumor</text>
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                <text>Roberts HJ; Wang Y; Spruit JL; Taylor L; Franson AT</text>
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                <text>BACKGROUND: Palliative care (PC) provides numerous benefits for children with cancer. Pediatric patients with high-grade glioma (HGG) are particularly well suited for early PC involvement given their high symptom burden and poor prognosis. However, studies continue to reveal that children with cancer, including HGG, have delayed PC involvement. We hypothesized that clinical trial enrollment may lead to a lack of or delay in PC involvement in this population. PROCEDURE: For each patient in our cohort of 43 pediatric patients with HGG, demographic, diagnostic, therapeutic, clinical trial enrollment, and PC information were collected. Statistical analysis was performed comparing PC characteristics between patients who did and did not enroll in a clinical trial. RESULTS: Seventy-two percent of patients had at least one visit with a PC provider. Fifty-six percent of patients enrolled in a clinical trial with HGG-directed therapy. Seventy-one percent of patients who enrolled in a clinical trial received specialty PC compared to 74% of non-trial participants (p = 1.000). Patients who enrolled in clinical trials received PC earlier in their disease course measured in days before death (mean = 177 days) compared to those who did not enroll (mean = 113 days, p = .180), though not statistically significant. CONCLUSIONS: The prevalence of clinical trial enrollment is high in patients with HGG and will likely increase as the genomic/epigenomic landscape of these tumors is better understood. As such, our data reassuringly suggest that trial participation does not interfere with the receipt of specialty PC in this population.</text>
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                <text>&lt;a href="http://doi.org/10.1002/pbc.30115" target="_blank" rel="noreferrer noopener"&gt;10.1002/pbc.30115&lt;/a&gt;</text>
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                <text>Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).</text>
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        <name>Child</name>
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        <name>Clinical Trial</name>
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        <name>Disease Progression</name>
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        <name>Glioma</name>
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        <name>Glioma/therapy/pathology</name>
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