» Articles » PMID: 26296147

Initial Experience With Gallium-68 DOTA-Octreotate PET/CT and Peptide Receptor Radionuclide Therapy for Pediatric Patients With Refractory Metastatic Neuroblastoma

Overview
Specialty Pediatrics
Date 2015 Aug 22
PMID 26296147
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

Rationale: Pediatric patients with refractory neuroblastoma have limited therapeutic options. Neuroblastoma may express somatostatin receptors (SSTRs) allowing imaging with 68Ga-DOTA-Octreotate (GaTATE) positron emission tomography/computed tomography (PET/CT) and peptide receptor radionuclide therapy (PRRT). We reviewed our experience with this theranostic combination.

Materials And Methods: GaTATE studies (8 patients; 2 to 9 years old) were reviewed and compared with 123I-MIBG or posttreatment 131I-MIBG studies. Immunohistochemistry (IHC) for SSTR subtype 2 was performed in 5 patients. Four patients received PRRT.

Results: GaTATE PET showed additional disease in 38% (3/8 patients), and upstaged 1 patient by detecting marrow involvement. IHC detected SSTR 2 in all patients assessed. Six patients were deemed suitable for PRRT on imaging. Four patients received 17 cycles of palliative PRRT (10 111In-DOTATATE; 5 177Lu-DOTATATE; 1 combined 111In and 177Lu-DOTATATE; 1 combined 177Lu and 90Y-DOTATATE) with no significant toxicity attributed to PRRT. All had objective responses. Two survivors are now 40 and 56 months from PRRT commencement.

Conclusions: GaTATE PET was positive in a high proportion of patients with refractory neuroblastoma, correlating with SSTR 2 on IHC, with additional disease identified compared with MIBG imaging. PRRT seems safe, feasible, with responses observed in patients with progression despite multimodality treatment. These data support ongoing clinical trials in such patients.

Citing Articles

Case report: Peptide receptor radioligand therapy in metastatic pediatric neuroendocrine tumors.

Hlongwa K, Kolade O, Alnabulsi A, Steyn R, Brink A, Prasad V Front Nucl Med. 2024; 3:1193880.

PMID: 39355026 PMC: 11440991. DOI: 10.3389/fnume.2023.1193880.


Heterogeneous SSTR2 target expression and a novel :: fusion clone in a progressive metastatic lesion following Lutetium-DOTATATE molecular radiotherapy in neuroblastoma: a case report.

Park S, Fransson S, Sundquist F, Nilsson J, Gryback P, Wessman S Front Oncol. 2024; 14:1408729.

PMID: 39324010 PMC: 11422106. DOI: 10.3389/fonc.2024.1408729.


Exploring innovative strides in radiolabeled nanoparticle progress for multimodality cancer imaging and theranostic applications.

Najdian A, Beiki D, Abbasi M, Gholamrezanezhad A, Ahmadzadehfar H, Amani A Cancer Imaging. 2024; 24(1):127.

PMID: 39304961 PMC: 11416024. DOI: 10.1186/s40644-024-00762-z.


p53 stabilisation potentiates [Lu]Lu-DOTATATE treatment in neuroblastoma xenografts.

Berglund H, Salomonsson S, Mohajershojai T, Gago F, Lane D, Nestor M Eur J Nucl Med Mol Imaging. 2023; 51(3):768-778.

PMID: 37823909 PMC: 10796565. DOI: 10.1007/s00259-023-06462-3.


A genome-wide CRISPR/Cas9 screen identifies DNA-PK as a sensitiser to Lutetium-DOTA-octreotate radionuclide therapy.

Waldeck K, Van Zuylekom J, Cullinane C, Gulati T, Simpson K, Tothill R Theranostics. 2023; 13(14):4745-4761.

PMID: 37771787 PMC: 10526672. DOI: 10.7150/thno.84628.