Imaging-Based Prevalence of Oligometastatic Disease: A Single-Center Cross-Sectional Study.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
15 11 2022
Historique:
received: 11 03 2022
revised: 25 05 2022
accepted: 26 06 2022
pubmed: 1 8 2022
medline: 19 10 2022
entrez: 31 7 2022
Statut: ppublish

Résumé

Oligometastatic disease refers to a distinct state in patients with cancer characterized by a low metastatic burden, with diagnosis being informed by a limited number of distant metastases in radiologic imaging. However, oligometastasis remains poorly understood in terms of its biology and prevalence in the metastatic cascade. In the absence of clinically viable molecular biomarkers, this study examined the prevalence of oligometastasis using oncological imaging. This study is based on all consecutive [fluorine-18]-fluorodeoxyglucose (FDG)- and [gallium-68]-prostate specific membrane antigen (PSMA)-positron emission tomography (PET) scans conducted at our cancer center between January and December 2020. We identified and analyzed all PET scans from patients with a maximum of 5 distant metastases from a solid malignancy and also reviewed concurrent cranial magnetic resonance imaging (cMRI) imaging in all candidate patients. Data on the number and sites of metastases were extracted from the imaging reports and verified on imaging studies in case of uncertainties. In total, 7000 PET scans were analyzed, of which 1155 were performed in unique metastatic patients, and 637 patients showed extracranial oligometastatic disease (55%). Concurrent cMRI scans were available for 20% (130/637) of extracranial oligometastatic patients, 36 of which proved to be polymetastatic after combined PET and cMRI analysis. Prevalence of oligometastatic disease was influenced by primary tumor histology and was most frequent in pancreatic, liver and gallbladder cancers (59%), but was least frequent in cancer of unknown primary (26%). In 72% of oligometastatic cases, only 1 or 2 metastases were detected. Bone/soft tissue metastases were the most common sites of distant metastasis (41%). About 75% of patients had metachronous oligometastatic disease. Our analysis suggests that about half of patients with metastatic cancer are characterized by a limited tumor burden detectable on PET and cMRI imaging. This finding warrants intensified research efforts to better understand the biology of oligometastatic disease and to optimize multidisciplinary treatment strategies.

Identifiants

pubmed: 35908582
pii: S0360-3016(22)00719-2
doi: 10.1016/j.ijrobp.2022.06.100
pii:
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

596-602

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Sebastian M Christ (SM)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland. Electronic address: sebastian.christ@usz.ch.

Kaspar Pohl (K)

Faculty of Medicine, University of Zurich, Zurich, Switzerland.

Urs J Muehlematter (UJ)

Department of Nuclear Medicine, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Philip Heesen (P)

Faculty of Medicine, University of Zurich, Zurich, Switzerland.

Anja Kühnis (A)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Jonas Willmann (J)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Maiwand Ahmadsei (M)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Eugenia Vlaskou Badra (EV)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Stephanie G C Kroeze (SGC)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Michael Mayinger (M)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Nicolaus Andratschke (N)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Martin Huellner (M)

Department of Nuclear Medicine, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Matthias Guckenberger (M)

Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

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Classifications MeSH