Detection of a second primary cancer in a 18F-fluorocholine PET/CT - multicentre retrospective analysis on a group of 1345 prostate cancer patients.


Journal

Nuclear medicine review. Central & Eastern Europe
ISSN: 1644-4345
Titre abrégé: Nucl Med Rev Cent East Eur
Pays: Poland
ID NLM: 100886103

Informations de publication

Date de publication:
2022
Historique:
received: 04 08 2021
accepted: 30 11 2021
entrez: 9 2 2022
pubmed: 10 2 2022
medline: 11 2 2022
Statut: ppublish

Résumé

Aim of this study was to evaluate the rate of incidental detection of second primary cancer (SPC) at 18F-fluorocholine ([18F]FCH) positron emission tomography/computed tomography (PET/CT) performed in prostate cancer patients. A retrospective analysis was performed on a group of 1345 prostate cancer patients, who underwent [18F]FCH PET/CT study because of suspicion of recurrence (n = 937) or for initial staging (n = 408). Images were acquired after intravenous injection [18F]FCH with a mean activity of 200 ± 75 MBq (5.4 ± 2 mCi), from the top of the head to the half of the thigh. The confirmation of second primary cancer was obtained from the cancer registry. Based on the [18F]FCH PET/CT scans, a second primary cancer was suspected in 89 patients (6.6%). Of these, a malignancy was histologically confirmed in 26 patients (29% of all suspected findings and 1.9% of the complete cohort). Lung cancer (including adenocarcinoma, neuroendocrine cancer) was diagnosed in 13 patients (50%) and hematologic neoplasm (including chronic lymphocytic leukemia, Hodgkin lymphoma, follicular lymphoma, and multiple myeloma) in 5 patients (19%). 18F-fluorocholine PET/CT also revealed esophageal cancer, mesothelioma, testicular, renal, bladder, and colorectal cancer inindividual patients, non-keratinizing squamous cell carcinoma (SCC) of the skin as well as head and neck SCC with unknown primary. We conclude that incidental detection of a second primary cancer in prostate cancer patients using [18F]FCH PET/CT is not very common and that lung cancer and hematologic malignancies are most frequently detected.

Sections du résumé

BACKGROUND BACKGROUND
Aim of this study was to evaluate the rate of incidental detection of second primary cancer (SPC) at 18F-fluorocholine ([18F]FCH) positron emission tomography/computed tomography (PET/CT) performed in prostate cancer patients.
MATERIAL AND METHODS METHODS
A retrospective analysis was performed on a group of 1345 prostate cancer patients, who underwent [18F]FCH PET/CT study because of suspicion of recurrence (n = 937) or for initial staging (n = 408). Images were acquired after intravenous injection [18F]FCH with a mean activity of 200 ± 75 MBq (5.4 ± 2 mCi), from the top of the head to the half of the thigh. The confirmation of second primary cancer was obtained from the cancer registry.
RESULTS RESULTS
Based on the [18F]FCH PET/CT scans, a second primary cancer was suspected in 89 patients (6.6%). Of these, a malignancy was histologically confirmed in 26 patients (29% of all suspected findings and 1.9% of the complete cohort). Lung cancer (including adenocarcinoma, neuroendocrine cancer) was diagnosed in 13 patients (50%) and hematologic neoplasm (including chronic lymphocytic leukemia, Hodgkin lymphoma, follicular lymphoma, and multiple myeloma) in 5 patients (19%). 18F-fluorocholine PET/CT also revealed esophageal cancer, mesothelioma, testicular, renal, bladder, and colorectal cancer inindividual patients, non-keratinizing squamous cell carcinoma (SCC) of the skin as well as head and neck SCC with unknown primary.
CONCLUSION CONCLUSIONS
We conclude that incidental detection of a second primary cancer in prostate cancer patients using [18F]FCH PET/CT is not very common and that lung cancer and hematologic malignancies are most frequently detected.

Identifiants

pubmed: 35137934
pii: VM/OJS/J/85172
doi: 10.5603/NMR.a2022.0006
doi:

Substances chimiques

fluorocholine 6029HGL0QP
Choline N91BDP6H0X

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

25-30

Auteurs

Paulina Cegla (P)

Department of Nuclear Medicine, Greater Poland Cancer Center, Poznan, Poland. paulina.cegla@gmail.com.

Katarzyna Scibisz-Dziedzic (K)

Chair and Department of Nuclear Medicine, Medical University of Lublin, Lublin, Poland.

Kamila Witkowska (K)

Department of Nuclear Medicine, Affidea Poznan, Poland.

Anna Kubiak (A)

Greater Poland Cancer Registry, Greater Poland Cancer Centre, Poznan, Poland.

Ewa Wierzchoslawska (E)

Department of Electroradiology, Poznan University of Medical Sciences, Poznan, Poland.
Radiology Department, Greater Poland Cancer Centre, Poznan, Poznań, Poland.

Witold Kycler (W)

Gastrointestinal Surgical Oncology Department, Greater Poland Cancer Centre, Poznan, Poland.
Department of Head and Neck Surgery, Poznan University of Medical Sciences, Poznan, Poland.

Beata Chrapko (B)

Chair and Department of Nuclear Medicine, Medical University of Lublin, Lublin, Poland.

Rafał Czepczyński (R)

Department of Nuclear Medicine, Affidea Poznan, Poland.
Department of Endocrinology, Metabolism and Internal Medicine, Poznan University of Medical Sciences, Poznan, Poland.

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Classifications MeSH