Comparison of renal clearance of [F]AlF-RESCA-HER2-BCH and [F]AlF-NOTA-HER2-BCH in mice and breast cancer patients
Creators
- 1. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), NMPA Key Laboratory for Research and Evaluation of Radiopharmaceuticals (National Medical Products Administration), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing (China)
- 2. Guizhou University School of Medicine, Guizhou University, Guiyang (China)
- 3. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Biochemistry and Molecular Biology, Peking University Cancer Hospital & Institute, Beijing (China)
- 4. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Breast Oncology, Peking University Cancer Hospital & Institute, Beijing (China)
Description
A novel HER2 affibody-based molecular probe, [F]AlF-RESCA-HER2-BCH, was developed for reducing renal uptake, evaluated, and compared with [F]AlF-NOTA-HER2-BCH. In preclinical studies, micro-PET/CT was performed using HER2-positive gastric cancer patient-derived xenografts (PDX) model at 0.5-1 (dynamic), 2, 4, and 6 h post-injection. For blocking experiment, 0.5 mg cold affibody was co-injected with probes. Biodistribution were performed on HER2-positive PDX models at 2 h post-injection. For clinical study, PET/CT images were acquired at 2 h and 4 h after injection of 231.29 ± 17.77 MBq [F]AlF-NOTA-HER2-BCH or [F]AlF-RESCA-HER2-BCH in five breast cancer patients (4 HER2-positive and 1 HER2-low). Standardized uptake values (SUVs) were measured in tumors and source-organs for semi-quantitative analysis. The OLINDA/EXM software (version 1.2) was used to calculate the radiation doses. [F]AlF-NOTA-HER2-BCH and [F]AlF-RESCA-HER2-BCH were stably labeled with [F]F, with high binding specificity and affinity to HER2. Micro-PET/CT of both tracers could clearly visualize HER2-positive PDX tumors with high uptake of 16.24 ± 1.74% ID/g and 14.39 ± 2.45% ID/g at 2 h post-injection. The renal accumulation of [F]AlF-RESCA-HER2-BCH was significantly lower than that of [F]AlF-NOTA-HER2-BCH (5.16 ± 0.22% ID/g vs. 158.73 ± 5.44% ID/g at 2 h, p < 0.0001). In the clinical study, both [F]AlF-NOTA-HER2-BCH and [F]AlF-RESCA-HER2-BCH demonstrated favorable tumor targeting and image contrast. [F]AlF-RESCA-HER2-BCH showed a higher SUVmax in both primary tumor and metastases, and a significantly higher target-to-nontarget ratio in metastases than [F]AlF-NOTA-HER2-BCH. Moreover, [F]AlF-RESCA-HER2-BCH had lower renal accumulation (43.56 ± 7.88 vs. 79.81 ± 3.81 at 2 h, p < 0.0001; 33.23 ± 6.89 vs. 78.63 ± 4.00 at 4 h, p < 0.0001) as well as a significantly lower renal absorbed dose than [F]AlF-NOTA-HER2-BCH (0.4450 ± 0.1117 mGy/MBq vs. 0.8030 ± 0.1604 mGy/MBq, p < 0.01). [F]AlF-RESCA-HER2-BCH tended to provide better image contrast than [F]AlF-NOTA-HER2-BCH with a higher target-to-nontarget ratio in detection of metastases. Notably, [F]AlF-RESCA-HER2-BCH had lower renal accumulation than [F]AlF-NOTA-HER2-BCH.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-023-06232-1Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 50
- Journal Issue
- 9
- Journal Page Range
- p. 2775-2786
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 54089676
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ABSORBED RADIATION DOSES; CARCINOMAS; COMPARATIVE EVALUATIONS; COMPUTER CODES; DATA COMPILATION; FLUORINE 18; IMAGE PROCESSING; KIDNEYS; MAMMARY GLANDS; METASTASES; MICE; PATIENTS; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; RENAL CLEARANCE; SPECIFICITY; UPTAKE
- Descriptors DEC
- ANIMALS; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CLEARANCE; COMPUTERIZED TOMOGRAPHY; DATA; DATA PROCESSING; DIAGNOSTIC TECHNIQUES; DISEASES; DOSES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; EVALUATION; EXCRETION; FLUORINE ISOTOPES; GLANDS; HOURS LIVING RADIOISOTOPES; INFORMATION; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MAMMALS; MATERIALS; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANS; PROCESSING; RADIATION DOSES; RADIOACTIVE MATERIALS; RADIOISOTOPES; RODENTS; TOMOGRAPHY; VERTEBRATES
Optional Information
- Notes
- Oncology #En Dash# General