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Poster session 11

1414P - Treatment efficacy and safety of 177Lu-PSMA radioligand therapy in octogenarians with metastatic castration-resistant prostate cancer

Date

10 Sep 2022

Session

Poster session 11

Topics

Clinical Research;  Cancer Treatment in Patients with Comorbidities;  Multi-Disciplinary and Multi-Professional Cancer Care;  Cancer in Older Adults;  Image-Guided Therapy

Tumour Site

Prostate Cancer

Presenters

Robert Tauber

Citation

Annals of Oncology (2022) 33 (suppl_7): S616-S652. 10.1016/annonc/annonc1070

Authors

R.L. Tauber1, M. Retz1, K. Knorr2, C. D’Alessandria2, S. Grigorascu2, K. Hansen2, H. Wester3, J. Gschwend1, W. Weber2, M. Eiber2, T. Langbein2

Author affiliations

  • 1 Urology, Klinikum Rechts der Isar - Technische Universitaet Muenchen, 81675 - Munich/DE
  • 2 Nuclear Medicine, Klinikum Rechts der Isar - Technische Universitaet Muenchen, 81675 - Munich/DE
  • 3 Tum School Of Natural Sciences - Radiopharmacy, TUM - Technical University of Munich, 80333 - Munich/DE

Resources

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Abstract 1414P

Background

Lutetium-177 prostate-specific membrane antigen radioligand therapy (177Lu-PSMA-RLT) is an option for treatment of metastatic castration-resistant prostate cancer (mCRPC). It is increasingly used in old or comorbid patients. Purpose was to evaluate the safety and efficacy in patients ≥80 years of age.

Methods

Seventy-nine mCRPC patients who underwent 177-lutetium–labeled PSMA-I&T RLT at the age of 80 or older (median age 82, IQR:81-84) between March 2016 and September 2021 were selected from our institutional database. Patients were previously treated with androgen receptor-directed therapy and taxane-based chemotherapy or were chemotherapy-ineligible. All patients showed high PSMA-ligand uptake at PSMA-PET. Treatment was performed with a total of 344 cycles (median 4 cycles, range:1–12) and a median activity of 27.9 GBq (IQR:14.9-43.9) on a 4 to 6 weeks interval base. Toxicity data were acquired until 6 months after last treatment. Best PSA-response, progression-free survival (PFS) and overall survival (OS) were obtained.

Results

Median number of previous mCRPC treatment regimens was two, 50/79 (63.3%) patients were chemotherapy-naïve (CTx-naïve) before Lu-177-PSMA therapy, 14/79 (17.7%) patients had visceral metastases. A PSA decline of 90% was achieved in 25/79 (31.6%), a 50%-PSA decline in 38/79 (48.1%) patients. CTx-naïve patients showed higher PSA response rates compared to CTx-pretreated patients (55.1% vs. 44.0% 50%-PSA-decline). Median PFS and OS were 9.5 and 16.5 months. Median PFS and OS of CTx-naïve patients were significantly longer compared to CTx-pretreated patients (11.3 months vs. 6.4 months and 20.4 vs. 14.0 months, respectively, both p<0.01). Treatment related grade 3 toxicities were anemia in 4/79 (5%), thrombocytopenia in 3/79 (4%) and chronic renal impairment in 6/79 (8%) patients, no nonhematologic grade 3 and no grade 4 toxicities were observed. Most frequent clinical side effects were grade 1-2 xerostomia, fatigue and inappetence.

Conclusions

Response rates and toxicity of 177Lu-PSMA RLT in old mCRPC patients are comparable to published data. Chemotherapy-naïve patients showed a better and longer response to therapy than chemotherapy-pretreated patients.

Clinical trial identification

Legal entity responsible for the study

Klinikum Rechts der Isar, Technichal University Munich.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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