Lutetium 177 (177Lu)-PSMA therapy is increasingly being adopted for patients with metastatic prostate cancer. Although therapy results have been encouraging, there is still room for optimization, particularly regarding tracer uptake and absorbed dose to the salivary glands. The concept of using a small molecular weight albumin-binding entity attached to the PSMA ligand to enhance the blood-circulation time was the basis for development of 177Lu-PSMA-ALB-56[a], which is a PSMA radioligand with higher tumor accumulation compared to other established PSMA ligands with relatively low background retention. Ten patients with metastatic castration resistant prostate cancer (mCRPC) were treated with a single dose of approximately 3.3 GBq (89.1 mCi) of 177Lu-PSMA-ALB-56 followed by sequential quantitative SPECT/CT acquisition at 1.5 hours, 6 hours, 24 hours, and 48 hours as well as 7 days following therapy administration in order to calculate tracer time activity curves (TACs) for tumor and critical organs for dosimetry evaluation. Quantitative SPECT/CT-based dosimetry for 3 such patients is highlighted in this clinical case review.
Whole-body (WB) SPECT/CT scans were acquired (3 bed positions from the top of the head to the upper thighs: 90 projections and 25 seconds per projection) on a Symbia™ SPECT/CT at approximately 1.5 hours, 6 hours, 24 hours, 48 hours, and at 7 days post-therapy administration with a 177Lu reference standard of approximately 10 MBq within the field of view (FOV). A medium-energy low-penetration (MELP) collimator was used with an acquisition of 3 energy windows with the peak window width of 20% centered around the 208 keV energy peak and 2 adjacent corresponding lower- and upper-scatter energy windows of 10% width.
All SPECT images were co-registered to the CT images. Volumes of interest (VOIs) were generated around the kidneys (left and right), liver, spleen, salivary glands (left and right parotid and submandibular glands), and up to 5 tumor lesions per patient with segmentation performed with either the SPECT or CT image. Total counts within VOIs obtained from sequential SPECT/CT images were converted to Bq/ml using phantom study derived calibration factor. TACs were generated from all VOIs. All TACs were fitted depending on the degree of correlation to a mono- or bi-exponential function. The cumulated activity for each source organ and tumor was determined by calculating the area under the curve of the fitted TAC. The normalized cumulated activity or residence time was calculated for all source organs and tumors as the cumulated activity divided by the administered activity. The absorbed organ doses and effective dose calculations were performed using OLINDA/EXM 1.1® software. Tumors were assumed to be spherical, and their volumes were calculated with sphere diameters based on the aver-age of the 2 longest diameters in the axial view on contrast-enhanced CT images. Additionally, tumor masses were calculated with either a density of 1.06 g/cm3 for soft-tissue lesions or 1.92 g/cm3 (same as cortical bone) for bone lesions.
An approximately 70-year-old male was referred with large para-aortic lymph node metastases along with left supraclavicular node metastases. Small focal bone metastases are also visualized in the sternum, right transverse process of the T7 vertebra, and the left iliac crest. All nodal and bone metastases show high 177Lu-PSMA-ALB-56 uptake in sequential SPECT/CT images. Tracer concentrations and volumes derived from sequential SPECT/CT data were used to generate TACs for subsequent dosimetry calculations. Calculated average absorbed dose to the para-aortic nodal metastases was 69.8 Gy/GBq while that to the supraclavicular metastases was 23.6 Gy/GBq. Average absorbed dose to bilateral renal cortex was 2.43 Gy/GBq. For an administered dose of 3.3 GBq, the absorbed dose to the largest tumor lesion (para-aortic nodal mass) was approximately 230 Gy, which is extremely high for a single therapy cycle.1 Renal cortical dose was calculated to be approximately 8 Gy. Among salivary glands, the left parotid gland received a high absorbed dose of 0.72Gy/GBq while the right parotid gland received 0.63 Gy/GBq. Bone marrow dose was higher than expected (0.30 Gy/GBq) with marrow dose predicted to be approximately 1 Gy for a single therapy cycle. In view of the 2 Gy cumulative bone marrow dose limitation threshold,2 the high marrow dose estimation is a cause for concern and close hematological monitoring during subsequent therapy cycles.
Follow-up evaluation of serum PSA shows a 15% decrease after 10 weeks after therapy administration. There was no significant renal or bone marrow toxicity.
An approximately 60-year-old male with mCRPC with pelvic bone metastases along with mediastinal lymph node metastases underwent 177Lu-PSMA-ALB-56 therapy. Following administration of 3.4 GBq (91.8 mCi) of 177Lu PSMA-ALB-56, sequential multi-bed SPECT/CT was performed at 90 minutes, 6 hours, 24 hours, 48 hours, and 7 days.
Dosimetry results show the bone metastases in the right ileum received an absorbed dose of 0.42 Gy/GBq (1.38 Gy for a single therapy cycle of 3.3 GBq), which is low for a 3.3 GBq therapy; however, the low retention of tracer within bone metastases on the 7-day image correlates well with the calculated absorbed dose. The mediastinal nodal metastases received a high dose of 9.52 Gy/GBq, which resulted in a predicted absorbed dose of 31.4 Gy for a 3.3 GBq therapy dose. The average renal cortical absorbed dose was 2.95 Gy/Gbq (9.7 Gy for single therapy cycle), which was higher than expected, suggesting the risk of crossing the 23 Gy renal absorbed dose limit within 3 cycles, assuming similar renal cortical doses in subsequent therapies. Renal dose can vary significantly compared to the initial cycle since the tumor burden may decrease with higher tracer clearance through the kidneys leading to higher renal dose. Average bone marrow dose was calculated to be 0.24 Gy/GBq (0.8 Gy for single therapy cycle), which was higher than expected considering the presence of a single bone metastasis. Salivary gland doses were moderate. The left parotid gland received an absorbed dose of 0.77 Gy/GBq while the right parotid gland received 0.64 Gy/GBq.
An approximately 75-year-old male with mCRPC with multiple bone and liver metastases was administered 3.6 GBq (97.2 mCi) of 177Lu PSMA-ALB-56. Sequential quantitative SPECT/CT was acquired based on the acquisition protocol followed in the preceding cases.
Dosimetry results show the average renal cortical absorbed dose of 2.09 Gy/GBq (6.8 Gy for the single therapy cycle). This was slightly higher than expected with implication that 2 more therapies would lead to the maximum allowed cumulative renal dose of 23 Gy,3 assuming a similar cortical dose for subsequent therapies. The largest bone metastases in the lumbar vertebrae received an absorbed dose of 8.14 Gy/GBq (26.8 Gy for the single therapy cycle) while the slightly smaller thoracic vertebral metastases received 6.97 Gy/GBq. Average bone marrow dose was calculated to be 0.27Gy/GBq (0.89 Gy for single therapy), which was quite high, reflecting the presence of multiple bone metastases impacting the dose to functioning marrow. Salivary gland doses were also significantly higher than expected as both the left and right parotid glands received an absorbed dose of approximately 0.80 Gy/GBq.
The clinical cases discussed here are part of 10 cases representing the first clinical application of 177Lu PSMA-ALB-56, which is a modified PSMA ligand with the aim of increasing the accumulation in tumor lesions. The cases demonstrate that the use of 177Lu PSMA-ALB-56 successfully achieved a 1.4 to 2.3-fold higher absorbed dose to tumor lesions (6.64 Gy/GBq on average) as compared with published values for 177Lu-PSMA-617 (3.87 Gy/GBq). The lesions considered for dosimetry among these patients were all larger than 1.5 ml in volume in order to reduce partial-volume effects. Of the 10 cases treated with a single therapy cycle of 177Lu PSMA-ALB-56, the mean absorbed kidney dose of 2.55+/- 0.93 Gy/GBq was about 3.3 times higher than that reported for 177Lu PSMA-617 (0.60-0.88 Gy/GBq), resulting in a mean tumor to kidney dose ratio of 3.3, which is lower than the reported dose ratio of 5.1 for 177Lu PSMA-617.4
The higher renal dose highlights the need for measures like amino-acid infusion and diuresis to reduce renal toxicity. Follow-up of these 10 patients after 1 cycle of approximately 3.3 GBq of 177Lu-PSMA-ALB-56 demonstrated a decrease in serum PSA values in 78% of patients with greater than 50% reduction in 44% of the patients. This observation is comparable to previous studies showing 77% of patients having a decrease in serum PSA after a single cycle of 7.5 GBq of 177Lu PSMA-617.5 The efficacy observed for 177Lu PSMA-ALB-56, administered at approximately 45% less activity was thus comparable to that of 177Lu PSMA-617.
Quantitative SPECT/CT is key to obtaining accurate TACs for subsequent dosimetry. Symbia SPECT/CT enabled multibed SPECT/CT acquisitions with accurate CT attenuation correction and scatter correction along with collimator detector response modeling to obtain SPECT/CT data that could be used to obtain quantitative information on tracer concentration in Bq/ml. Quantitative multibed WB SPECT/CT data could be used in commercially available dosimetry software for accurate absorbed dose calculation. Considering the higher tumor absorbed dose possibility with 177Lu PSMA-ALB-56, there is potential of improving radionuclide therapy of metastatic prostate cancer using such radioligands, although higher renal and salivary dose considerations need to be considered. In such situations, accurate dosimetry using sequential SPECT/CT is of key importance for improving therapeutic outcomes while avoiding toxicity.
Scanner: Symbia SPECT/CT
3.3 GBq (89.1 mCi) 177Lu-PSMA-ALB-56
90 minutes, 6 hours, 24 hours, 48 hours, 7 days
90 projections, 25 seconds per projection
59 ref mAs
2 x 4 mm
The outcomes achieved by the Siemens Healthineers customer described herein were achieved in the customer’s unique setting. Since there is no “typical” hospital and many variables exist (eg, hospital size, case mix, level of IT adoption) there can be no guarantee that others will achieve the same results.