TY - JOUR
T1 - Diagnosis of bone metastases in breast cancer
T2 - Lesion-based sensitivity of dual-timepoint FDG-PET/CT compared to low-dose CT and bone scintigraphy
AU - Hansen, Jeanette Ansholm
AU - Naghavi-Behzad, Mohammad
AU - Gerke, Oke
AU - Baun, Christina
AU - Falch, Kirsten
AU - Duvnjak, Sandra
AU - Alavi, Abass
AU - Høilund-Carlsen, Poul Flemming
AU - Hildebrandt, Malene Grubbe
N1 - Publisher Copyright:
© 2021 Hansen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2021/11/18
Y1 - 2021/11/18
N2 - We compared lesion-based sensitivity of dual-time-point FDG-PET/CT, bone scintigraphy (BS), and low-dose CT (LDCT) for detection of various types of bone metastases in patients with metastatic breast cancer. Prospectively, we included 18 patients with recurrent breast cancer who underwent dual-time-point FDG-PET/CT with LDCT and BS within a median time interval of three days. A total of 488 bone lesions were detected on any of the modalities and were categorized by the LDCT into osteolytic, osteosclerotic, mixed morphologic, and CT-negative lesions. Lesion-based sensitivity was 98.2% (95.4-99.3) and 98.8% (96.8-99.5) for early and delayed FDG-PET/CT, respectively, compared with 79.9% (51.1- 93.8) for LDCT, 76.0% (36.3-94.6) for BS, and 98.6% (95.4-99.6) for the combined BS +LDCT. BS detected only 51.2% of osteolytic lesions which was significantly lower than other metastatic types. SUVs were significantly higher for all lesion types on delayed scans than on early scans (P<0.0001). Osteolytic and mixed-type lesions had higher SUVs than osteosclerotic and CT-negative metastases at both time-points. FDG-PET/CT had significantly higher lesion-based sensitivity than LDCT and BS, while a combination of the two yielded sensitivity comparable to that of FDG-PET/CT. Therefore, FDG-PET/CT could be considered as a sensitive one-stop-shop in case of clinical suspicion of bone metastases in breast cancer patients.
AB - We compared lesion-based sensitivity of dual-time-point FDG-PET/CT, bone scintigraphy (BS), and low-dose CT (LDCT) for detection of various types of bone metastases in patients with metastatic breast cancer. Prospectively, we included 18 patients with recurrent breast cancer who underwent dual-time-point FDG-PET/CT with LDCT and BS within a median time interval of three days. A total of 488 bone lesions were detected on any of the modalities and were categorized by the LDCT into osteolytic, osteosclerotic, mixed morphologic, and CT-negative lesions. Lesion-based sensitivity was 98.2% (95.4-99.3) and 98.8% (96.8-99.5) for early and delayed FDG-PET/CT, respectively, compared with 79.9% (51.1- 93.8) for LDCT, 76.0% (36.3-94.6) for BS, and 98.6% (95.4-99.6) for the combined BS +LDCT. BS detected only 51.2% of osteolytic lesions which was significantly lower than other metastatic types. SUVs were significantly higher for all lesion types on delayed scans than on early scans (P<0.0001). Osteolytic and mixed-type lesions had higher SUVs than osteosclerotic and CT-negative metastases at both time-points. FDG-PET/CT had significantly higher lesion-based sensitivity than LDCT and BS, while a combination of the two yielded sensitivity comparable to that of FDG-PET/CT. Therefore, FDG-PET/CT could be considered as a sensitive one-stop-shop in case of clinical suspicion of bone metastases in breast cancer patients.
KW - Bone Neoplasms/diagnostic imaging
KW - Bone and Bones/cytology
KW - Breast/cytology
KW - Breast Neoplasms/complications
KW - Diagnostic Tests, Routine/methods
KW - Female
KW - Fluorodeoxyglucose F18
KW - Humans
KW - Neoplasm Metastasis/diagnostic imaging
KW - Neoplasm Recurrence, Local/diagnostic imaging
KW - Positron Emission Tomography Computed Tomography/methods
KW - Positron-Emission Tomography/methods
KW - Radionuclide Imaging/methods
KW - Sensitivity and Specificity
KW - Tomography, X-Ray Computed/methods
UR - http://www.scopus.com/inward/record.url?scp=85119506684&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0260066
DO - 10.1371/journal.pone.0260066
M3 - Journal article
C2 - 34793550
AN - SCOPUS:85119506684
SN - 1932-6203
VL - 16
SP - e0260066
JO - PLoS One
JF - PLoS One
IS - 11 November
M1 - e0260066
ER -