TY - JOUR
T1 - Baseline Imaging Derived Predictive Factors of Response Following [Lu-177]Lu-PSMA-617 Therapy in Salvage Metastatic Castration-Resistant Prostate Cancer: A Lesion- and Patient-Based Analysis
T2 - A Lesion- and Patient-Based Analysis
AU - van der Sar, Esmée C.A.
AU - Kühr, Adinda J.S.
AU - Ebbers, Sander C.
AU - Henderson, Andrew M.
AU - Keizer, Bart de
AU - Lam, Marnix G.E.H.
AU - Braat, Arthur J.A.T.
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/7
Y1 - 2022/7
N2 - Earlier studies have mostly identified pre-therapeutic clinical and laboratory parameters for the prediction of treatment response to [
177Lu]Lu-PSMA-617 in metastatic castration resistant prostate cancer patients (mCRPC). The current study investigated whether imaging-derived factors on baseline [
68Ga]Ga-PSMA-11 PET/CT can potentially predict the response after two cycles of [
177Lu]Lu-PSMA-617 treatment, in a lesion- and patient-based analysis in men with mCRPC. Included patients had histologically proven mCRPC and a [
68Ga]Ga-PSMA-11 PET/CT before and after two cycles of [
177Lu]Lu-PSMA-617 treatment. The imaging-based response was evaluated on lesion-level (standardized uptake value (SUV) reduction) and patient-level (total lesion PSMA (TL-PSMA) reduction). In the lesion-level analysis, a clear relationship was found between SUV
peak/max and the imaging-based response to [
68Ga]Ga-PSMA-11 PET/CT (most avid lesion SUV
peak/max ≥ 30% reduction) (
p < 0.001), with no significant difference in cut-off values between different sites of metastases (i.e., lymph node, bone or visceral metastasis). In patient-level analysis, baseline PSA and SUV
peak values of most avid metastasis were significantly associated with imaging-based response (TL-PSMA ≥ 30% reduction) (
p = 0.019 and
p = 0.015). In pre-treatment with [
68Ga]Ga-PSMA-11 PET/CT, a clear accumulation-response relationship in lesion-level was found for SUV
peak/max in men with mCRPC receiving two cycles of [
177Lu]Lu-PSMA-617 treatment. The SUV
peak of the most avid lesion was the only image-derived factor predictive of the imaging-based response at the patient-level.
AB - Earlier studies have mostly identified pre-therapeutic clinical and laboratory parameters for the prediction of treatment response to [
177Lu]Lu-PSMA-617 in metastatic castration resistant prostate cancer patients (mCRPC). The current study investigated whether imaging-derived factors on baseline [
68Ga]Ga-PSMA-11 PET/CT can potentially predict the response after two cycles of [
177Lu]Lu-PSMA-617 treatment, in a lesion- and patient-based analysis in men with mCRPC. Included patients had histologically proven mCRPC and a [
68Ga]Ga-PSMA-11 PET/CT before and after two cycles of [
177Lu]Lu-PSMA-617 treatment. The imaging-based response was evaluated on lesion-level (standardized uptake value (SUV) reduction) and patient-level (total lesion PSMA (TL-PSMA) reduction). In the lesion-level analysis, a clear relationship was found between SUV
peak/max and the imaging-based response to [
68Ga]Ga-PSMA-11 PET/CT (most avid lesion SUV
peak/max ≥ 30% reduction) (
p < 0.001), with no significant difference in cut-off values between different sites of metastases (i.e., lymph node, bone or visceral metastasis). In patient-level analysis, baseline PSA and SUV
peak values of most avid metastasis were significantly associated with imaging-based response (TL-PSMA ≥ 30% reduction) (
p = 0.019 and
p = 0.015). In pre-treatment with [
68Ga]Ga-PSMA-11 PET/CT, a clear accumulation-response relationship in lesion-level was found for SUV
peak/max in men with mCRPC receiving two cycles of [
177Lu]Lu-PSMA-617 treatment. The SUV
peak of the most avid lesion was the only image-derived factor predictive of the imaging-based response at the patient-level.
KW - lutetium
KW - predictors
KW - prostate cancer
KW - prostate specific membrane antigen
KW - radio-ligand therapy
UR - http://www.scopus.com/inward/record.url?scp=85134736107&partnerID=8YFLogxK
U2 - 10.3390/biomedicines10071575
DO - 10.3390/biomedicines10071575
M3 - Article
C2 - 35884878
AN - SCOPUS:85134736107
SN - 2227-9059
VL - 10
SP - 1
EP - 16
JO - Biomedicines
JF - Biomedicines
IS - 7
M1 - 1575
ER -