TY - JOUR
T1 - Delayed Imaging Improves Lesion Detectability in [99mTc]Tc-PSMA-I&S SPECT/CT in Recurrent Prostate Cancer
AU - Berliner, Christoph
AU - Steinhelfer, Lisa
AU - Chantadisai, Maythinee
AU - Kroenke, Markus
AU - Koehler, Daniel
AU - Pose, Randi
AU - Bannas, Peter
AU - Knipper, Sophie
AU - Eiber, Matthias
AU - Maurer, Tobias
N1 - Publisher Copyright:
COPYRIGHT ß 2023 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2023/7/1
Y1 - 2023/7/1
N2 - Our objective was to compare the ability to detect histopathologically confirmed lymph node metastases by early and delayed [99mTc]Tc-PSMA-I&S SPECT/CT in early biochemically recurrent prostate cancer. Methods: We retrospectively analyzed 222 patients selected for radioguided surgery using [99mTc]Tc-PSMA-I&S SPECT/CT at different time points after injection (#4 h and .15 h). In total, 386 prostate-specific membrane antigen (PSMA) PET predetermined lesions were analyzed on SPECT/CT using a 4-point scale, and the results were compared between early and late imaging groups, with uni- and multivariate analyses performed including prostate-specific antigen, injected [99mTc]Tc-PSMA-I&S activity, Gleason grade group, initial TNM stage, and, stratified by size, PSMA PET/CT–positive lymph nodes. PSMA PET/CT findings served as the standard of reference. Results: [99mTc]Tc-PSMA-I&S SPECT/CT had a significantly higher positivity rate for detecting lesions in the late than the early imaging group (79%, n 5 140/178, vs. 27%, n 5 12/44 [P, 0.05] on a patient basis; 60%, n 5 195/324, vs. 21%, n 5 13/62 [P, 0.05] on a lesion basis). Similar positivity rates were found when lesions were stratified by size. Multivariate analysis found that SUVmax on PSMA PET/CT and the uptake time of [99mTc]Tc-PSMA-I&S were independent predictors for lesion detectability on SPECT/CT. Conclusion: Late imaging (.15 h after injection) should be preferred when [99mTc]Tc-PSMA-I&S SPECT/CT is used for lesion detection in early biochemical recurrence of prostate cancer. However, the performance of PSMA SPECT/CT is clearly inferior to that of PSMA PET/CT.
AB - Our objective was to compare the ability to detect histopathologically confirmed lymph node metastases by early and delayed [99mTc]Tc-PSMA-I&S SPECT/CT in early biochemically recurrent prostate cancer. Methods: We retrospectively analyzed 222 patients selected for radioguided surgery using [99mTc]Tc-PSMA-I&S SPECT/CT at different time points after injection (#4 h and .15 h). In total, 386 prostate-specific membrane antigen (PSMA) PET predetermined lesions were analyzed on SPECT/CT using a 4-point scale, and the results were compared between early and late imaging groups, with uni- and multivariate analyses performed including prostate-specific antigen, injected [99mTc]Tc-PSMA-I&S activity, Gleason grade group, initial TNM stage, and, stratified by size, PSMA PET/CT–positive lymph nodes. PSMA PET/CT findings served as the standard of reference. Results: [99mTc]Tc-PSMA-I&S SPECT/CT had a significantly higher positivity rate for detecting lesions in the late than the early imaging group (79%, n 5 140/178, vs. 27%, n 5 12/44 [P, 0.05] on a patient basis; 60%, n 5 195/324, vs. 21%, n 5 13/62 [P, 0.05] on a lesion basis). Similar positivity rates were found when lesions were stratified by size. Multivariate analysis found that SUVmax on PSMA PET/CT and the uptake time of [99mTc]Tc-PSMA-I&S were independent predictors for lesion detectability on SPECT/CT. Conclusion: Late imaging (.15 h after injection) should be preferred when [99mTc]Tc-PSMA-I&S SPECT/CT is used for lesion detection in early biochemical recurrence of prostate cancer. However, the performance of PSMA SPECT/CT is clearly inferior to that of PSMA PET/CT.
KW - PET
KW - biochemical recurrence
KW - prostate carcinoma
KW - radioguided
KW - salvage surgery
KW - scintigraphy
UR - http://www.scopus.com/inward/record.url?scp=85164210075&partnerID=8YFLogxK
U2 - 10.2967/jnumed.122.265252
DO - 10.2967/jnumed.122.265252
M3 - Article
C2 - 37230531
AN - SCOPUS:85164210075
SN - 0161-5505
VL - 64
SP - 1036
EP - 1042
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 7
ER -