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Poster session 15

1823P - The impact of baseline PSMA PET/CT vs. CT on outcomes of Radium-223 therapy in mCRPC patients

Date

21 Oct 2023

Session

Poster session 15

Topics

Radiological Imaging;  Nuclear Medicine and Clinical Molecular Imaging;  Staging Procedures;  Therapy

Tumour Site

Prostate Cancer

Presenters

Dianne Bosch

Citation

Annals of Oncology (2023) 34 (suppl_2): S954-S1000. 10.1016/S0923-7534(23)01946-4

Authors

D. Bosch1, K. van der Velden1, I.M. Oving2, D.N.J. Wyndaele3, L.E. Weijs4, D.W. van Schelven5, W.J.G. Oyen6, E.T. te Beek7, D.M. Somford8, J. Nagarajah9, R. Hermsen10, N. Mehra11, W.R. Gerritsen12, M.J. van der Doelen1, I.M. van Oort1

Author affiliations

  • 1 Urology Dept., Radboud University Medical Center, 6525 GA - Nijmegen/NL
  • 2 Internal Medicine Dept, Ziekenhuisgroep Twente (ZGT), 7609PP - Almelo/NL
  • 3 Nuclear Medicine, Catharina Hospital Eindhoven, 5602 ZA - Eindhoven/NL
  • 4 Nuclear Medicine, Ziekenhuisgroep Twente (ZGT), 7609PP - Almelo/NL
  • 5 Nuclear Medicine, Noorderbreedte, 8932 PJ - Leeuwarden/NL
  • 6 Nuclear Medicine, Rijnstate Hospital, 6815 AD - Arnhem/NL
  • 7 Nuclear Medicine, Reinier de Graaf Hospital, 2625 AD - Delft/NL
  • 8 Urology, Canisius Wilhelmina Ziekenhuis CWZ Hospital, 6532 SZ - Nijmegen/NL
  • 9 Nuclear Medicine, Department of Medical Imaging, Radboud University Medical Center, 6525 GA - Nijmegen/NL
  • 10 Nuclear Medicine, Canisius Wilhelmina Ziekenhuis CWZ Hospital, 6532 SZ - Nijmegen/NL
  • 11 Medical Oncology Department, Radboud University Medical Center, Nijmegen, 6525 GA - Nijmegen/NL
  • 12 Consultancy, CimCure B.V., 1081 HV - Amsterdam/NL

Resources

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Abstract 1823P

Background

Imaging prior to Radium-223 therapy (Ra-223) is crucial for selecting metastatic castration-resistant prostate cancer (mCRPC) patients with bone-only disease. The purpose of this study was to evaluate if baseline PSMA PET/CT versus CT is associated with biochemical response during Ra-223.

Methods

A secondary analysis of the data of a prospective observational study (NCT04995614) was performed. Patients received a maximum of six cycles of Ra-223 and were retrospectively divided into the PSMA PET/CT (bPSMA) or CT (bCT) group based on baseline imaging technique. All patients received baseline bone scintigraphy. Primary endpoints were alkaline phosphatase (ALP) and prostate specific antigen (PSA) response, defined as ≥ 30% decline from baseline. Secondary endpoints were overall survival (OS) and radiological response.

Results

Between 2017 and 2020, 122 mCRPC patients were included: 18 (14.8%) in the bPSMA and 104 (85.2%) in the bCT group. All baseline characteristics were comparable. No significant differences in ALP or PSA response were found between the groups. The bCT group showed a significant shorter OS compared to the bPSMA group (12.4 vs.19.9 months, p < 0.01, table). Post-therapy soft tissue involvement (STI) was detected in 29/76 patients (38.2%) that received bCT and post-therapy CT (bCT/pCT), compared to 0/18 bPSMA patients. No significant difference in OS was found between bCT/pCT patients without STI and bPSMA patients. Table: 1823P

OS (months) among subgroups

Baseline imaging Post-therapy imaging N Median OS (IQR) P-value
PSMA Total PSMA A. STI B. W/o STI CT C. STI D. W/o STI No imaging 18 11/18 0/11 11/11 4/18 0/4 4/4 3/18 19.9 (12.7 – 29.0) - - 21.2 (14.7 – 40.8) - - 20.3 (15.2 – 36.8) 4.9 (3.1 - NR) 0.038 vs. bCT - - - - - - -
CT Total PSMA A. STI B. W/o STI CT C. STI D. W/o STI E. Unknown STI No imaging 104 7/104 6/7 1/7 76/104 29/76 44/76 3/76 21/104 12.4 (7.9 – 18.2) - 14.6 (11.5 – 24.9) 21.5 (NR) - 10.6 (6.0 – 14.2) 14.8 (9.3 – 26.0) - 9.2 (4.0 – 12.9) 0.038 vs. bPSMA - - - - <0.01 vs. bCT/pCT w/o STI 0.457 vs. bPSMA - -

Abbreviations: W/o, without; NR, not reached.

Conclusions

bPSMA versus bCT does not seem to predict biochemical response during Ra-223. Nevertheless, patients in the bCT group had a significantly shorter OS, most likely due to underdetection of STI in this group. Therefore, replacing baseline CT with PSMA PET/CT appears to be a valuable screening method to ensure in-label use of Ra-223.

Clinical trial identification

NCT04995614.

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Bayer.

Disclosure

D. Bosch: Financial Interests, Personal, Invited Speaker: MSD AstraZeneca. W.J.G. Oyen: Financial Interests, Personal and Institutional, Speaker, Consultant, Advisor: Bayer, AAA Novartis. D.M. Somford: Financial Interests, Personal, Advisory Board: Janssen Pharmaceuticals, Bayer, Astellas; Financial Interests, Institutional, Research Grant: Astellas. R. Hermsen: Financial Interests, Personal, Advisory Board: Bayer; Financial Interests, Personal, Other, Personal fees and travel expenses: Bayer. N. Mehra: Financial Interests, Personal and Institutional, Advisory Board, And personal fees and research funding: Bayer; Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal and Institutional, Advisory Board, And research grants and personal fees: Roche, Merck Sharp and Dohme; Financial Interests, Personal and Institutional, Advisory Board, And research grants, research funding and personal fees: Astellas, Janssen Pharmaceuticals; Financial Interests, Personal and Institutional, Other, Research grants and personal fees: AstraZeneca, Sanofi; Financial Interests, Institutional, Research Grant: Pfizer, Genzyme. W.R. Gerritsen: Financial Interests, Personal, Advisory Board: BMS, Sanofi Gemzyme, Amgen, Morphosys and CureVac; Financial Interests, Personal and Institutional, Advisory Board, Plus research funding: Astellas, Janssen Pharmaceuticals; Financial Interests, Personal and Institutional, Advisory Board, Plus research funding and speaker fees: Bayer; Financial Interests, Personal, Invited Speaker: MSD. M.J. van der Doelen: Financial Interests, Institutional, Research Grant: Bayer, Janssen Pharmaceuticals; Financial Interests, Personal, Other, Speaker fees: Astellas. I.M. van Oort: Financial Interests, Personal and Institutional, Advisory Board, Plus research funding: MSD/AstraZeneca; Financial Interests, Personal and Institutional, Research Grant, Plus research funding and personal fees: Astellas, Bayer; Financial Interests, Personal and Institutional, Research Grant, Plus personal fees: Janssen Pharmaceuticals; Financial Interests, Personal and Institutional, Research Funding: Pfizer; Financial Interests, Institutional, Research Funding: AAA Novartis. All other authors have declared no conflicts of interest.

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