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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 on OpenAlex· 10.1093/noajnl/vdac085

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

The three-model screen

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All three models called this out of scope.

stratum: aff_core · design weight: 5595.24 (the sample is stratified; any rate computed without the weight is wrong)
Claude Opus 4.8OUT
genre: empirical
about Canada: no
confidence: high

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

GPT-5.6 (high)OUT
genre: empirical
about Canada: no
confidence: high

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

Grok 4.5OUT
genre: empirical
about Canada: no
confidence: high

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

Abstract

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.

Stored with the screening record, where it is evidence for the labels above.

The record

Venue
Neuro-Oncology Advances
Topic
Virus-based gene therapy research
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Oncolytics Biotech (Canada)
Funders
National Cancer InstituteCancer Research UKOncolytics BiotechMayo Clinic
Keywords
MedicineLeukopeniaNeutropeniaRefractory (planetary science)Adverse effectGliomaInternal medicineOncolytic virusToxicitySurgeryCancer
Has abstract in OpenAlex
yes