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Theranostics 2021; 11(17):8143-8151. doi:10.7150/thno.60222 This issue Cite

Research Paper

Total tumor volume reduction and low PSMA expression in patients receiving Lu-PSMA therapy

Robert Seifert^1,2,3,4, Katharina Kessel², Katrin Schlack^4,5, Matthias Weckesser^2,4, David Kersting^1,3,4, Konstantin E. Seitzer^4,5, Manuel Weber^1,3,4, Martin Bögemann^4,5, Kambiz Rahbar^2,4

1. Department of Nuclear Medicine, University Hospital Essen, Essen, Germany
2. Department of Nuclear Medicine, University Hospital Münster, Münster, Germany
3. German Cancer Consortium (DKTK)
4. West German Cancer Center
5. Department of Urology, University Hospital Münster, Münster, Germany

✉ Corresponding author: Kambiz Rahbar MD, Department of Nuclear Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, D-48149 Münster, Germany. Tel: +49-251-8347362; Fax: +49-251-8347363; rahbarde

Abstract

Background: [¹⁷⁷Lu]-PSMA-617 (Lu-PSMA) therapy is a promising therapeutic option for end-stage prostate cancer patients. Early treatment response at the first restaging after two therapy cycles might correlate with high treatment efficacy and long overall survival (OS). Therefore, the aim of this study was to evaluate whether early reduction in tumor volume is a positive prognosticator for OS. To this end, PSMA PET prior to therapy (baseline) and at first restaging after two therapy cycles (interim; i.e., 12 weeks) were compared.

Methods: Patients with metastatic castration-resistant prostate cancer who received Lu-PSMA therapy were reviewed for this analysis. All patients with available baseline and interim [⁶⁸Ga]-PSMA-11 PET/CT were included in this analysis (n = 33). All PSMA avid metastases in baseline and interim PETs were semi-automatically segmented. The average PSMA expression (mean SUV_max of all metastases), total tumor volume (PSMA-TV) and TLQ (quotients of tumor volume and SUV_mean summed over all metastases) were quantified at baseline and interim timepoints. Response in PSMA-TV was assumed when a decline > 30% was present. OS and biochemical response were available for all patients.

Results: Baseline PSMA-TV was a statistically significant prognosticator of OS (HR = 1.618 95%CI: 1.117 - 2.343, p = 0.011). Reduction in PSMA-TV was not a statistically significant positive prognosticator of OS in the total cohort (HR = 0.829 95%CI: 0.559 - 1.230, p = 0.352). Likewise, there was no statistical difference in survival time comparing patients with PSMA-TV response to those without (13.2 vs. 15.6 months, p = 0.1). In the subgroup of patients with PSMA-TV response, mean SUV_max was a statistically significant prognosticator of OS (binarized by median; HR = 0.15; 95%CI: 0.03 - 0.83; p < 0.05). If patients with low PSMA expression at baseline were excluded from the analysis, reduction in PSMA-TV became a positive prognosticator of OS in uni- and multivariable Cox regression (HR = 0.290; 95%CI: 0.108 - 0.782; p = 0.015).

Conclusion: PSMA-TV reduction was a positive prognosticator of OS only if patients with low PSMA expression were excluded. This might indicate that the PSMA-PETs of patients with low PSMA expression may not be suited for assessing PSMA-TV reduction. Future studies investigating the interplay of PSMA-TV and low PSMA expression response are warranted.

Keywords: ¹⁷⁷Lu-PSMA-617, mCRPC, radioligand therapy

Introduction

Patients with metastasized castration-resistant prostate cancer (mCRPC) ultimately undergo progression and most likely have a fatal outcome [1]. However, [¹⁷⁷Lu]Lutetium PSMA-617 (Lu-PSMA) radioligand therapy or similar ligands like PSMA I&T that target the prostate-specific membrane antigen (PSMA) are showing high biochemical response rates (up to 66%) and have a favorable toxicity profile in mCRPC patients [2-8]. Yet, the monitoring of treatment response to Lu-PSMA therapy and outcome prognostication is a clinical issue that has to date been inadequately addressed.

Recently, PSMA targeting positron emission tomography (PET) criteria have been proposed to assess the treatment responses of patients with mCRPC [9, 10]. These criteria recommend the integration of PSMA PET derived total tumor volume as a metric to monitor the course of the disease. We and others could show that baseline PSMA PET derived tumor volume quantification is feasible and that pretherapeutic tumor volume is a statistically significant prognosticator of outcome in patients treated with Lu-PSMA therapy [11-13].

Preliminary data suggests that PSMA PET derived total tumor volume (PSMA-TV) changes can be employed to monitor treatment response to Lu-PSMA therapy [14, 15]. However, Schmuck et al. only included ten patients for tumor volume monitoring under Lu-PSMA therapy and Grubmüller et al. employed an unusual interim PET timepoint after the third administration of Lu-PSMA therapy [14, 15]. Therefore, a comprehensive analysis of the implications of PSMA-TV changes between baseline and interim PET after two cycles of Lu-PSMA therapy is still missing.

Early decrease of PSMA-TV may indicate response, but could also be caused by low PSMA expression due to cancer cell dedifferentiation and thus be associated with short OS. We showed previously that initially low PSMA expression may be a statistically significant negative prognosticator of overall survival (OS) [16]. However, the interplay of PSMA-TV reduction and PSMA expression is poorly elucidated to date.

Therefore, the aim of the present study was to compare baseline and interim PSMA PET derived PSMA-TV to assess whether prolonged OS is associated with PSMA-TV response. Additionally, the PSMA expression of patients with PSMA-TV response was investigated.

Methods

Patients

All patients who received Lu-PSMA therapy in the Department of Nuclear Medicine of the University Hospital Münster were selected for this study if baseline and interim PSMA-11 PET CT were present. A total number of 33 patients met these inclusion criteria. Detailed patient characteristic data is provided in Table 1.

PSMA PET acquisition

PSMA PET imaging and tracer synthesis was done as previously reported [11]. Briefly, [⁶⁸Ga]Gallium-PSMA-11 was employed for PET imaging. The PSMA-11 precursor was delivered by ABX (ABX GmbH, Radeberg, Germany). Image acquisition started 60 minutes after injection using a Biograph mCT (Siemens Healthineers, Knoxville, TN, United States). The PET scan area included the vertex to thigh. A mean dose of 163 (standard deviation: 24) MBq was administered. Whole-body low dose and abdominal full dose (contrast-enhanced) PET acquisitions were obtained.

PSMA therapy

Prostate cancer patients referred to the Department of Nuclear Medicine Münster for Lu-PSMA therapy were treated with PSMA-617 (ABX advanced biochemical compounds, Radeberg, Germany) conjugated with [¹⁷⁷Lu]Lutetium (ITG Isotopes Technology, Garching, Germany). The Lu-PSMA therapy was administered at a 6-8 weeks interval.

Image interpretation

Sixty-six PSMA PET CTs were semi-automatically analyzed as previously published (33 baseline and 33 interim PETs) [11]. The software research prototype MICIIS was employed for image analysis (formerly MI Whole Body Analysis Suite, MIWBAS, Siemens Healthineers, Knoxville, TN, United States). Briefly, all foci with increased PSMA uptake were automatically segmented employing a liver-specific threshold, which leads to the segmentation of physiological and pathological foci (i.e. all lesions with an SUV_max greater than the liver threshold were segmented). The liver-specific segmentation threshold was automatically determined (threshold = (4.3 / liver SUV_mean) × (liver SUV_mean + liver SUV_{standard deviation}). Tracer foci caused by physiological uptake were semi-automatically removed from the analysis: As previously published, foci within the kidney, spleen and liver can be automatically removed. A trained nuclear medicine physician then manually checked the preliminary segmentation and adjusted the result if needed. Adjustments typically included the re-segmentation of liver metastases and the exclusion of gastrointestinal tracer uptake. Thereby, only metastases were segmented ultimately. For each selected focus, 50% of the local SUV_max was used to segment the metastasis. TLQ_lesion (total lesion quotient) was defined as the quotient of metabolic tumor volume and the SUV_mean of a given focus as previously reported [12]. For each metastasis, SUV_max, TLQ_lesion and metabolic tumor volume were noted. For each PSMA PET acquisition, the metrics of all metastases were summed to obtain the total tumor volume (PSMA-TV) and TLQ metric, or averaged to obtain mean SUV_max. Volumetric response was defined as a decline greater than 30% comparing baseline and interim PSMA PET, as previously published by Grubmüller et al. [17]. Additionally, the 30% decline criterion is also employed by RECIST and PERCIST and seems to be justified by SUV repeatability measurements of PSMA PET [18-20].

Statistical analysis

R (version 4.0.3) was used for descriptive analysis, Wilcoxon test, Spearman correlation, Cox regression, Martingale analysis and plotting [21]. For the cutoff finding of continuous variables, the R package “maxstat” was used. For Cox regression and Martingale analysis, response in PSMA-TV was expressed as a ratio (PSMA‑TV_baseline / PSMA‑TV_interim). All parameters were log transformed for Cox regression and Martingale analysis. P < 0.05 was used as the significance level.

Results

Patient characteristics at baseline and interim time point

Detailed patient characteristics are provided in Table 1. The baseline median PSMA-TV was 138 ml (IQR = 230 ml), the interim median PSMA-TV was 107 ml (IQR = 199 ml). The median OS of the entire cohort was 15 (8.6 - 25.9) months.

Association of baseline PSMA PET derived parameters and overall survival

Baseline PSMA-TV was a statistically significant negative prognosticator of OS in univariate Cox regression (HR = 1.618 95%CI: 1.117 - 2.343, p = 0.011). Baseline mean SUV_max was not a statistically significant prognosticator of OS in univariate Cox regression (HR = 0.416 95%CI: 0.133 - 1.30, p = 0.131). Multivariable regressions of baseline PET derived parameters (PSMA-TV, TLQ and mean SUV_max) adjusted for baseline blood tumor markers LDH and PSA are shown in Table 2. Only baseline TLQ remained a statistically significant prognosticator of OS in a multivariable regression adjusted for PSA and LDH levels (HR = 2.33; 95%CI: 1.23-4.42; p = 0.009). Supplemental Figure 1 shows a Martingale residual analysis.

To visualize the OS, the medians of baseline PSMA-TV and TLQ were used to group the patients with high or low PET metrics; Figure 1 shows the OS by Kaplan Meier plots. Patients with high PSMA-TV did not have shorter median OS compared to those with low tumor volume (13.2 vs. 25.9 months, p = 0.08; HR = 2.314, 95%CI: 0.885 - 6.049, p = 0.087). In contrast, patients with high mean SUV_max had longer OS compared to those without (22.5 vs. 11.4 months, p = 0.023; HR = 0.352, 95%CI: 0.138 - 0.899, p = 0.029).

Association of interim PSMA PET derived parameters and OS

Interim PSMA-TV was a statistically significant prognosticator of OS in univariate Cox regression (HR = 1.427 95%CI: 1.06 - 1.921, p = 0.019). Interim mean SUV_max was not a statistically significant prognosticator of OS in univariate Cox regression (HR = 0.963, 95%CI = 0.519 - 1.786, p = 0.904).

 Figure 1 

Baseline PET metrics and overall survival. Kaplan Meier plots of OS are shown for the total tumor volume (PSMA-TV, A) and the summed TLQ score (TLQ = quotient of tumor volume and SUV_mean of all metastases are summed, B). Median OS in months (mo) and log rank p values are shown additionally. For all panels, the median of the PET measurements was employed to distinguish between patients with high (yellow) and low (blue) values.

Association of total tumor volume (PSMA-TV) response with PSA response

A total number of 15 patients had a PSMA-TV tumor decline greater than 30%. The best relative PSA response and relative PSMA-TV_response were significantly correlated (Spearman ρ = 0.67; p < 0.001). Patients with biochemical response had significantly greater PSMA-TV decline compared to patients without biochemical response (-51% vs. 48%, p < 0.001). Additionally, patients with PSA response had significantly longer OS (25.5 vs. 11.4 months p < 0.05). See Figure 2C for details.

Association of total tumor volume (PSMA-TV) response with OS

PSMA-TV_response was not a statistically significant prognosticator of OS in univariate Cox regression (HR = 0.829 95%CI: 0.559 - 1.230, p = 0.352). Multivariable regression is shown in Table 3. PSMA-TV_response was not a statistically significant prognosticator for OS in a multivariable regression adjusted for PSA and LDH (p = 0.430). Martingale residual analysis is shown in supplemental Figure 1. Confirming expectations, patients with a tumor volume reduction did not have a significantly longer OS compared to those without (15.6 vs. 13.2 months, p = 0.1; HR = 0.475, 95%CI: 0.190 - 1.189, p = 0.112; see Figure 2D).

Association of total tumor volume (PSMA-TV) response and OS in patients without low PSMA expression

In total, 27 out of 33 patients had high mean SUV_max expression at baseline according to the previously published threshold (high PSMA expression: mean SUV_max > 14.3). Paradoxically, 20% of all PSMA-TV responding patients had low mean SUV_max expression at baseline, which is a known negative prognosticator of OS (Figure 3) [12, 16]. Table 4 shows the characteristics of PSMA-TV responding patients. In patients with PSMA-TV response, baseline mean SUV_max was a statistically significant prognosticator of OS (binarized by median; HR = 0.15; 95%CI: 0.03-0.83; p < 0.05). To investigate whether patients with low mean SUV_max influenced the prognostication of OS by exhibiting strong PSMA-TV reduction, patients with low mean SUV_max were excluded from the analysis. In the subgroup of patients without low PSMA expression (mean SUV_max > 14.3 according to Seifert et al.), the reduction of PSMA-TV was a statistically significant positive prognosticator of OS (HR = 0.378 95%CI: 0.169 - 0.848, p = 0.018) [16]. Moreover, PSMA-TV response remained a significant prognosticator in a multivariable analysis adjusted for baseline PSA and LDH levels (HR = 0.290 95%CI: 0.108 - 0.782, p = 0.015).

 Figure 2 

Response in the total tumor volume. The correlation of response in total tumor volume (PSMA-TV) and best PSA response is shown in panel A. The Waterfall plot (B) shows best PSA decline of the included cohort, yellow patients had a PSMA-TV decline of >30 %, whereas blue patients had not. Patients with PSA response have a significantly longer overall survival (C). Patients with a total tumor volume decline of greater 30% (Group 2, D) did not have a significantly longer OS compared to patients without (Group 1).

 Figure 3 

Divergence between tumor volume response and baseline stratification. Patients with low baseline meanSUV_max have a significantly shorter OS time (A). The median was used to seperate between patients with high (yellow) and low (blue) meanSUV_max. A considerable fraction of patients with tumor volume response greater than 30% had a high baseline TLQ and low meanSUVmax (B). Patients with a total tumor volume response of >30% were further stratified by low/high baseline TLQ (C) and low/high baseline meanSUV_max (D). To this end, the meanSUV_max and TLQ cutoffs to distinguish between patients with low and high values were determined by a log-rank cutoff finder (meanSUV_max threshold = 22.8; TLQ threshold = 34.4); this binarization was only done for visualization purposes. Despite presence of volumetric tumor response, baseline TLQ and meanSUV_max identified patients at risk of poor outcome.

 Figure 4 

PSMA expression. An exemplary patient is shown before (A) and after (B) Lu-PSMA therapy. The patient had a low baseline PSMA expression and high TLQ. The MIP of the PSMA -PET acquisition is shown with and without segmented metastases (marked in red). After Lu-PSMA therapy, the PSMA expression decreased, and the diffuse bone marrow involvement (blue arrows) has only minimal PSMA uptake. Therefore, less tumor volume is segmented, which erroneously suggested PSMA-TV response.

Discussion

The reduction in PSMA PET derived total tumor volume (PSMA-TV) in response to [¹⁷⁷Lu]Lutetium-PSMA617 therapy was evaluated as a prognosticator for OS in the present study. To this end, the pretherapeutic (baseline) and interim PSMA PET/CTs after two cycles of Lu-PSMA therapy were compared. If the entire cohort was regarded, PSMA-TV reduction was surprisingly not a relevant prognosticator of OS. If patients with low PSMA expression were excluded from the analysis, PSMA-TV reduction was a statistically significant positive prognosticator of OS. Therefore, reduction of PSMA-TV appears to be a valuable parameter to prognosticate OS, but the clinician must carefully consider PSMA expression to avoid misleading interpretations of PSMA-TV reductions.

Lu-PSMA therapy is a promising therapeutic option for patients with advanced prostate cancer and has been evaluated in several retrospective and prospective studies [2, 7, 22]. However, the identification of patients who respond to Lu-PSMA is a clinical issue that has not been sufficiently addressed. Especially with the rise of other targeted therapeutics like Olaparib that might be alternatives to Lu-PSMA therapy, the long-term prediction of response and prognostication of outcome for patients prior to Lu-PSMA therapy is gaining importance [23]. Recently, the utilization of PSMA-TV has been proposed as a biomarker to assess therapy response [9]. Despite preliminary studies that identified the reduction in PSMA-TV as a prognosticator of OS, the interplay of PSMA-TV with the degree of PSMA expression is still poorly elucidated. Moreover, previously published studies have either suffered from small patient cohorts or a limited number of events (only 11 deaths out of 38 patients) [14, 15].

The present study indicates that baseline PSMA-TV is a statistically significant prognosticator of OS in patients treated with Lu-PSMA therapy. Surprisingly, the decrease of PSMA-TV was not a statistically significant prognosticator in the present cohort. To investigate these counterintuitive findings, the baseline PSMA expression of patients with tumor volume response and short overall survival was analyzed. We hypothesized that the reduction of PSMA-TV cannot be regarded without looking at the PSMA expression. The reason for this is that in advanced prostate cancer, cancer cells might undergo dedifferentiation and lose the ability to express PSMA [24, 25]. Therefore, PSMA-TV could be biased by the presence of unsegmentable metastases with faint PSMA expression.

The reduction of PSMA‑TV was a statistically significant prognosticator of OS in the present study in patients without low PSMA expression. This indicates that the reduction of PSMA‑TV in the interim PET can be erroneously interpreted as a treatment response in the presence of metastases with low PSMA expression at baseline (Figure 4). Patients with low baseline PSMA expression do not seem to be suited for interim PET tumor volumetry and PSMA-TV reduction quantification. Therefore, PSMA expression should be checked when the reduction of PSMA-TV in response to Lu-PSMA therapy is assessed. Future studies should evaluate whether PSMA-TV only captures metastases with sufficient PSMA uptake for Lu-PSMA therapy but neglects metastases with insufficient PSMA uptake.

Patients with a biochemical response (PSA decline greater than 50%) had a longer OS compared to patients without. This seems contradictory to the finding that patients with tumor volume response did not show a longer OS in the total cohort. However, the PSA value might more robustly quantify the tumor volume and may not be influenced by metastases with low PSMA expression. It must be noted that different PSMA-TV response thresholds than the commonly employed 30% decline might identify patients with short overall survival. However, given the reproducibility of PSMA PET metrics in the range of +/- 30%, only the 30 % cutoff was used for PSMA-TV in the present study [20].

The present study faces some limitations. There might be a selection bias, as only patients with two cycles of Lu-PSMA therapy were included. The reason for this is because restaging after the start of therapy is generally performed after the administration of the second cycle of Lu-PSMA therapy. Patients with rapid progression of prostate cancer, who might therefore not have received a second cycle of Lu-PSMA therapy, were not included. This might impair the transferability of the results to larger patient cohorts. Additionally, the included patient cohort is still relatively small. Because we only included patients who received PSMA-11 PET/CT at baseline and follow-up, patients who received combinations of PSMA-11 and PSMA-1007 PET CTs were not included in this study. However, given the high rate of events (60%), we feel that this limitation should not impair the findings of this study. A limitation of the PSMA PET volumetry is that only metastases with elevated PSMA expression are captured. Due to dedifferentiation and decreasing PSMA expression, the tumor volume might erroneously appear regredient, while the actual tumor volume is progredient. The contrary report of Grubmüller et al., who found PSMA-TV reduction to be associated with longer OS, might be partly explained by the more advanced cancer stages in our cohort (median LDH = 282 vs. 189 U/L; median PSA 146 vs. 61 ng/mL), which could correlate with a larger fraction of patients who show low PSMA expression [15]. Therefore, future studies should find new methods to measure the whole-body tumor volume in patients with low PSMA expression. Finally, we did not evaluate the occurrence of new metastases as extra category, which per se leads to a progredient disease rating. This contrasts with RECIST, in which the occurrence of new metastases automatically leads to progredient disease. However, RECIST cannot measure a total tumor volume but relies on exemplary lesions. Therefore, the new metastases criterion is needed to assess the disease status in RECIST. Future studies are needed to evaluate relevance of new metastases in the context of whole-body tumor volume measurements.

Conclusion

Decline in PSMA PET derived total tumor volume is not a prognosticator of OS in patients treated with Lu-PSMA therapy, if patients with low PSMA expression were included in the cohort. If patients with low PSMA expression were excluded, reduction in PSMA-TV is a significant prognosticator of OS, even in multivariable analysis. Therefore, PSMA-TV alone is not suited to monitor the progression of disease in end-stage prostate cancer patients. This might be due to erroneously quantified interim tumor volume reduction in the event of low PSMA uptake. Further studies focusing on the tumor volume response of patients with advanced prostate cancer are warranted. Tumor volume reduction should be carefully regarded in conjunction with baseline PSMA expression to properly assess treatment response.

Supplementary Material

Supplementary figure.

Acknowledgements

Disclosures

KR has received consultant fees from Bayer and lectureship fees from Janssen Cilag, Amgen, AAA and SIRTEX. KR is a clinical consultant for ABX. The University of Muenster has received consulting fees from ABX Advanced Biochemical Compounds, Radeberg, Germany for KR. MB has received consultant and lectureship fees from Bayer, Janssen Cilag, Astellas, ABX, Sanofi, Eisai, EUSApharm, Pfizer, BMS, MSD, AstraZeneca, Merck, Amgen, Novartis, Exelixis and Roche.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. This article does not contain any studies with animals performed by any of the authors. This study was approved by the local ethics committee (No. 2016-585-f-S and further amendments, Ethikkommission der Ärztekammer Westfalen-Lippe und der Westfälischen Wilhelms-Universität Münster).

Abbreviations

TV: Tumor Volume; PSMA: Prostate Specific Membrane Antigen.

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding author: Kambiz Rahbar MD, Department of Nuclear Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, D-48149 Münster, Germany. Tel: +49-251-8347362; Fax: +49-251-8347363; rahbarde

Received 2021-3-8
Accepted 2021-6-25
Published 2021-7-13

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