The relationship between tumour dosimetry, response, and overall survival in patients with unresectable Neuroendocrine Neoplasms (NEN) treated with

177Lu DOTATATE (LuTate) therapy Gastro-entero-pancreatic neuroendocrine neoplasm GEP NEN Peptide Receptor Radionuclide Therapy (PRRT) Radiopharmaceutical Dosimetry Radiosensitising Chemotherapy

Journal

European journal of nuclear medicine and molecular imaging
ISSN: 1619-7089
Titre abrégé: Eur J Nucl Med Mol Imaging
Pays: Germany
ID NLM: 101140988

Informations de publication

Date de publication:
08 2023
Historique:
received: 03 12 2022
accepted: 30 04 2023
medline: 31 7 2023
pubmed: 15 5 2023
entrez: 15 5 2023
Statut: ppublish

Résumé

Peptide Receptor Radionuclide Therapy (PRRT) delivers targeted radiation to Somatostatin Receptor (SSR) expressing Neuroendocrine Neoplasms (NEN). We sought to assess the predictive and prognostic implications of tumour dosimetry with respect to response by Patients with gastro-entero-pancreatic (GEP) NEN who received LuTate followed by quantitative SPECT/CT (Q-SPECT/CT) the next day (Jul 2010 to Jan 2019) were retrospectively reviewed. Single time-point (STP) lesional dosimetry was performed for each cycle using population-based pharmacokinetic modelling. MITV Median of 4 PRRT cycles were administered to 90 patients (range 2-5 cycles; mean 27.4 GBq cumulative activity; mean 7.6 GBq per cycle). 68% received at least one cycle with radiosensitising chemotherapy (RSC). RECIST 1.1 partial response was 24%, with 70% stable and 7% progressive disease. Cycle 1 radiation dose in measurable lesions was associated with local response (odds ratio 1.5 per 50 Gy [95% CI: 1.1-2.0], p = 0.002) when adjusted by tumour grade and RSC. Median change in MITV Radiation dose to tumour during PRRT was predictive of radiologic response but not survival. Survival outcomes may relate to other biological factors. There was no evidence that MITV

Identifiants

pubmed: 37184682
doi: 10.1007/s00259-023-06257-6
pii: 10.1007/s00259-023-06257-6
pmc: PMC10382388
doi:

Substances chimiques

copper dotatate CU-64 0
Organometallic Compounds 0
Octreotide RWM8CCW8GP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2997-3010

Informations de copyright

© 2023. The Author(s).

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Auteurs

R Alipour (R)

Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Australia. Ramin.Alipour@petermac.org.
The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia. Ramin.Alipour@petermac.org.

P Jackson (P)

Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Australia.
The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia.

M Bressel (M)

The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia.
Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.

A Hogg (A)

Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Australia.

J Callahan (J)

Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Australia.

R J Hicks (RJ)

Department of Medicine, St Vincent's Medical School, The University of Melbourne, Melbourne, Australia.

G Kong (G)

Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Australia.
The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia.

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Classifications MeSH