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Theranostics for Neuroblastoma: Making Molecular Radiotherapy Work Better.

作者信息

Gawne Peter J, Bryant Helen E, DuBois Steven G, George Sally L, Gray Juliet, Knox Leona, Matchett Kyle B, Peet Connie, Vallis Katherine A, Wallace Hugh J, Wan Simon, Gaze Mark N

机构信息

Centre for Cancer Biomarkers and Biotherapeutics, Barts Cancer Institute, Queen Mary, University of London, London, United Kingdom.

UCL Cancer Institute, University College London, London, United Kingdom.

出版信息

J Nucl Med. 2025 Apr 1;66(4):490-496. doi: 10.2967/jnumed.124.269121.


DOI:10.2967/jnumed.124.269121
PMID:39978816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11960609/
Abstract

Despite improvements in neuroblastoma treatment, survival figures lag behind those of many other childhood malignancies. New treatments, and better use of existing treatments, are essential to reduce mortality. Neuroblastoma expresses several molecular targets for radionuclide imaging and therapy, of which the most widely exploited is the norepinephrine transporter. [I]metaiodobenzylguanidine (MIBG) imaging and [I]MIBG treatment, which target this physiologic pathway, have been in clinical practice for 40 y. Although therapy outcomes have been favorable, [I]MIBG use has not yet been optimized. Somatostatin receptors and the disialoganglioside are alternative targets, but their use remains experimental. The charity Children's Cancer Research Fund organized a workshop bringing together a broad range of scientists including radiochemists, radiobiologists, radiation physicists, clinical researchers including pediatric oncologists and nuclear medicine physicians, and patient advocates from the United Kingdom, United States, and continental Europe to share their experiences with molecular imaging and radiotherapy of neuroblastoma and discuss potential ways of improving treatment outcomes and access. These include development of alternative vectors targeting somatostatin receptors and disialoganglioside, isotopes such as α-particle and Auger electron emitters with different radiation characteristics, and combinations with external-beam radiotherapy, immunotherapy, and DNA damage repair inhibitors. Barriers to progress discussed included the unpredictable radioisotope supply, production of novel radiopharmaceuticals, lack of data regarding which are the best combination therapies, and insufficient clinical facilities. The aim was to stimulate the development and assessment of more effective treatments.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7935/11960609/0e398f3cdbbf/jnumed.124.269121f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7935/11960609/74d4957503fb/jnumed.124.269121f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7935/11960609/0e398f3cdbbf/jnumed.124.269121f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7935/11960609/74d4957503fb/jnumed.124.269121f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7935/11960609/0e398f3cdbbf/jnumed.124.269121f2.jpg

相似文献

[1]
Theranostics for Neuroblastoma: Making Molecular Radiotherapy Work Better.

J Nucl Med. 2025-4-1

[2]
MIBG (metaiodobenzylguanidine) theranostics in pediatric and adult malignancies.

Br J Radiol. 2018-11

[3]
Radiolabeled metaiodobenzylguanidine for the treatment of neuroblastoma.

Nucl Med Biol. 2008-8

[4]
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[5]
Nuclear medicine procedures and neuroblastoma in childhood. Their value in the diagnosis, staging and assessment of response to therapy.

Q J Nucl Med. 2003-3

[6]
Comparison of ¹²³I-metaiodobenzylguanidine (MIBG) and ¹³¹I-MIBG semi-quantitative scores in predicting survival in patients with stage 4 neuroblastoma: a report from the Children's Oncology Group.

Pediatr Blood Cancer. 2011-2-15

[7]
[Radio iodized metaiodobenzylguanidine (MIBG) in the treatment of neuroblastoma: modalities and indications].

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[8]
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[9]
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[10]
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本文引用的文献

[1]
Patients, parents and professional perspectives on molecular radiotherapy for neuroblastoma and paediatric neuroendocrine cancers.

Nucl Med Commun. 2025-4-1

[2]
Response to PARP Inhibition in -Mutated Refractory Neuroblastoma.

N Engl J Med. 2024-8-15

[3]
Performing [F]MFBG Long-Axial-Field-of-View PET/CT Without Sedation or General Anesthesia for Imaging of Children with Neuroblastoma.

J Nucl Med. 2024-8-1

[4]
DNA-PK inhibitor AZD7648 is a more portent radiosensitizer than PARP inhibitor Olaparib in BRCA1/2 deficient tumors.

DNA Repair (Amst). 2024-7

[5]
A novel approach to guide GD2-targeted therapy in pediatric tumors by PET and [Cu]Cu-NOTA-ch14.18/CHO.

Theranostics. 2024

[6]
Improving susceptibility of neuroendocrine tumors to radionuclide therapies: personalized approaches towards complementary treatments.

Theranostics. 2024

[7]
The evidence-based role of catecholaminergic PET tracers in Neuroblastoma. A systematic review and a head-to-head comparison with mIBG scintigraphy.

Eur J Nucl Med Mol Imaging. 2024-2

[8]
Multimodal Therapy with Consolidating Haploidentical Stem Cell Transplantation and Dinutuximab Beta for Patients with High-Risk Neuroblastoma and Central Nervous System Relapse.

J Clin Med. 2023-9-25

[9]
Marshalling the Potential of Auger Electron Radiopharmaceutical Therapy.

J Nucl Med. 2023-9

[10]
Cervical Ganglioneuroblastoma Diagnosed by Ga-DOTATOC PET/CT in a Child with Opsoclonus Myoclonus Syndrome.

J Nucl Med Technol. 2023-12-5

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