Supplementary Figure 1 from Improving Global Access to Genomic Profiling in Rare Pediatric Cancers

Sameer Farouk Sait; Tara J. O’Donohue; Tejus Bale; Anita S. Bowman; Katherine E. Hill; Emily Stockfisch; Alexandra Giantini-Larsen; Tina Alano; Marc K. Rosenblum; Jamal Benhamida; Ira J. Dunkel; Michael F. Berger; Maria E. Arcila; Marc Ladanyi; Michael V. Ortiz; Julia Glade Bender; Alexandra Miller; Debyani Chakravarty; Kelly Cavender; Benjamin Preiser; Hongxin Zhang; Andrew L. Kung; David B. Solit; Matthias A. Karajannis; Neerav Shukla

doi:10.1158/1078-0432.29759998

Key Points

MAIN FINDING: The workflow enhances global access to genomic profiling for rare pediatric cancers.
KEY EVIDENCE: It outlines essential steps from patient outreach to results delivery for local physicians.
APPROACH: The workflow includes patient screening, enrollment, testing, and communication of results.
SIGNIFICANCE: Improving access to genomic profiling can lead to better treatment options for affected children.

Implication

Overview reveals the workflow for genomic profiling in rare pediatric cancers, indicating essential patient engagement steps.

Abstract

Supplementary Figure 1. Overview of the workflow involved from patient outreach, screening, enrollment, testing and return of results to local physician/patient.

Discussion

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Cite This Study

Sait et al. (2025) studied this question.

synapsesocial.com/papers/689a0c72e6551bb0af8d027d https://doi.org/10.1158/1078-0432.29759998

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Supplementary Figure 1 from Improving Global Access to Genomic Profiling in Rare Pediatric Cancers

Key Points

Implication

Abstract

Discussion

Cite This Study

Supplementary Figure 1 from Improving Global Access to Genomic Profiling in Rare Pediatric Cancers

Key Points

Implication

Abstract

Discussion

Cite This Study

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