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Phase I trial of sargramostim/pelareorep therapy in pediatric patients with recurrent or refractory high-grade brain tumors

2022· article· en· 29 citations· W4283020820 sur OpenAlex· 10.1093/noajnl/vdac085

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Le tri à trois modèles

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strate : aff_core · poids de sondage : 5595.24 (l'échantillon est stratifié ; tout taux calculé sans le poids est faux)
Claude Opus 4.8OUT
genre : empirical
porte sur le Canada: non
confiance: high

Phase I clinical trial of an oncolytic virus therapy in pediatric brain tumors.

GPT-5.6 (high)OUT
genre : empirical
porte sur le Canada: non
confiance: high

This is a phase I clinical trial of a brain-tumor therapy, not metaresearch.

Grok 4.5OUT
genre : empirical
porte sur le Canada: non
confiance: high

Phase I clinical trial of oncolytic therapy in pediatric brain tumours.

Résumé

Background: Brain tumors are the leading cause of cancer death for pediatric patients. Pelareorep, an immunomodulatory oncolytic reovirus, has intravenous efficacy in preclinical glioma models when preconditioned with GM-CSF (sargramostim). We report a phase I trial with the primary goal of evaluating the safety of sargramostim/pelareorep in pediatric patients with recurrent or refractory high-grade brain tumors and a secondary goal of characterizing immunologic responses. Methods: The trial was open to pediatric patients with recurrent or refractory high-grade brain tumors (3 + 3 cohort design). Each cycle included 3 days of subcutaneous sargramostim followed by 2 days of intravenous pelareorep. Laboratory studies and imaging were acquired upon recruitment and periodically thereafter. Results: ) were assessed. One patient experienced a dose limiting toxicity of persistent hyponatremia. Common low-grade (1 or 2) adverse events included transient fatigue, hypocalcemia, fever, flu-like symptoms, thrombocytopenia, and leukopenia. High-grade (3 or 4) adverse events included neutropenia, lymphopenia, leukopenia, hypophosphatemia, depressed level of consciousness, and confusion. All patients progressed on therapy after a median of 32.5 days and died a median of 108 days after recruitment. Imaging at progression did not show evidence of pseudoprogression or inflammation. Correlative assays revealed transient but consistent changes in immune cells across patients. Conclusions: Sargramostim/pelareorep was administered to pediatric patients with recurrent or refractory high-grade brain tumors. Hyponatremia was the only dose limiting toxicity (DLT), though maximum tolerated dose (MTD) was not determined.

Conservé avec la notice de tri, où il sert de preuve aux étiquettes ci-dessus.

La notice

Revue
Neuro-Oncology Advances
Thématique
Virus-based gene therapy research
Domaine
Biochemistry, Genetics and Molecular Biology
Établissements canadiens
Oncolytics Biotech (Canada)
Organismes subventionnaires
National Cancer InstituteCancer Research UKOncolytics BiotechMayo Clinic
Mots-clés
MedicineLeukopeniaNeutropeniaRefractory (planetary science)Adverse effectGliomaInternal medicineOncolytic virusToxicitySurgeryCancer
Résumé présent dans OpenAlex
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