Case Report: Evolution of intratumoral spatial heterogeneity assessed by [68Ga]Ga-DOTA-NOC PET/CT during dinutuximab beta therapy in pediatric high-risk neuroblastoma - Report - MDSpire
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Case Study: Changes in Intratumoral Spatial Heterogeneity Monitored by [68Ga]Ga-DOTA-NOC PET/CT During Dinutuximab Beta Treatment in Pediatric Patients with High-Risk Neuroblastoma
Clinical Report: Changes in Intratumoral Spatial Heterogeneity Monitored by [68Ga]Ga-DOTA-NOC PET/CT
Overview
This case study reports on a 4-year-old male with high-risk neuroblastoma who underwent monitoring with [68Ga]Ga-DOTA-NOC PET/CT during dinutuximab beta treatment. The primary tumor showed structural regression, while a focal area exhibited increased radiotracer uptake, indicating the presence of a viable, poorly differentiated neuroblastoma subclone.
Background
Neuroblastoma is a prevalent extracranial solid tumor in children, characterized by significant biological heterogeneity that can lead to treatment resistance. The use of [68Ga]Ga-DOTA-NOC PET/CT for assessing somatostatin receptor expression is being explored, particularly in the context of immunotherapy.
Data Highlights
Parameter
Baseline
Post-Treatment
SUVmax (Primary Tumor)
6.5
3.1
SUVmax (Focal Area)
N/A
17.4
Primary Tumor Dimensions
12.7 × 7.9 × 14.6 cm
7.0 × 3.9 × 6.8 cm
Key Findings
A 4-year-old male with high-risk neuroblastoma was monitored using [68Ga]Ga-DOTA-NOC PET/CT.
Post-treatment imaging showed structural regression of the primary tumor but increased uptake in a focal area.
The focal area with increased uptake was confirmed to contain viable, poorly differentiated neuroblastoma.
The findings emphasize the use of [68Ga]Ga-DOTA-NOC PET/CT for monitoring treatment response in neuroblastoma. Elevated SSTR uptake in residual tumors may indicate viable disease, warranting further investigation.
Conclusion
This case highlights the interpretation of imaging results in the context of immunotherapy for neuroblastoma. Enhanced SSTR expression following treatment may signify viable tumor subclones.