Evidence map›Paper›PMID 42459701›Full record

ArticleFrontiers in immunology2026

Management of persistent soft tissue residuals exhibiting an imaging paradox (^123I-MIBG-negative/^68Ga-DOTA-NOC-positive) in high-risk neuroblastoma following immunotherapy: a case report.

Si-Jia He, Ju Gao, Guo-Qian He, Xia Guo, Xiao-Yu Jing

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Si-Jia HeDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Ju GaoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Guo-Qian HeDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Xia GuoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Xiao-Yu JingDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Managing persistent soft tissue residual disease in high-risk neuroblastoma (HR-NB) remains a clinical challenge, particularly when conventional response assessments suggest remission but residual lesions persist. Determining whether such lesions represent inactive treatment-related changes or viable tumor has important implications for subsequent management. We report a 4-year-and-11-month-old girl with HR-NB who received multimodal therapy, including induction chemotherapy, surgery, radiotherapy, autologous stem cell transplantation, and seven cycles of dinutuximab beta-based immunotherapy. Following treatment, standard evaluations demonstrated complete bone marrow clearance and a ^123I-MIBG Curie score of 0, suggesting an excellent systemic response. However, a persistent paravertebral residual lesion remained detectable on imaging. Notably, ^68Ga-DOTA-NOC PET/CT demonstrated persistent tracer uptake despite negative ^123I-MIBG findings, creating an imaging discordance that raised concern for residual viable disease. Subsequent "third-look" surgical resection confirmed viable neuroblastoma within the lesion. Pathological examination revealed a markedly increased Ki-67 labeling index compared with the post-induction specimen (50% versus 8%), indicating persistent proliferative activity and suggesting biological heterogeneity within the residual lesion. This case highlights the diagnostic and therapeutic challenges posed by persistent soft tissue residual lesions after immunotherapy. The discordance between ^123I-MIBG and ^68Ga-DOTA-NOC imaging suggests that conventional imaging alone may not fully characterize selected residual lesions. In patients with persistent masses and discordant imaging findings, multimodal functional imaging may provide complementary information to guide clinical decision-making. The favorable outcome observed in this patient, who remains in sustained remission following surgical resection without additional antitumor therapy, supports consideration of an integrated management strategy combining multimodal imaging assessment and appropriately timed surgical intervention for selected cases of persistent residual disease.

Indexed as

3-IodobenzylguanidineImmunotherapyNeuroblastomaOrganometallic CompoundsSoft Tissue NeoplasmsAntibodies, MonoclonalChild, PreschoolCombined Modality TherapyFemaleHumansNeoplasm, ResidualPositron Emission Tomography Computed TomographyRadiopharmaceuticalsTreatment Outcome3-Iodobenzylguanidine68Ga-DOTANOCAntibodies, MonoclonaldinutuximabOrganometallic CompoundsRadiopharmaceuticals123I-MIBG68Ga-DOTA-NOC PET/CTanti-GD2 immunotherapyhigh-risk neuroblastomamultimodal imagingresidual disease

Identifiers

PMID42459701
PMCPMC13368866

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.