Outcomes of Cytoreductive Radical Prostatectomy for Oligometastatic Prostate Cancer on Prostate-specific Membrane Antigen Positron Emission Tomography: Results of a Multicenter European Study
Language English Country Netherlands Media print-electronic
Document type Journal Article, Multicenter Study
PubMed
37845121
DOI
10.1016/j.euo.2023.09.006
PII: S2588-9311(23)00197-9
Knihovny.cz E-resources
- Keywords
- Cytoreductive radical prostatectomy, Multimodal therapy, Oligometastatic, Prostate cancer, Prostate-specific membrane antigen positron emission tomography,
- MeSH
- Antigens, Surface metabolism MeSH
- Cytoreduction Surgical Procedures MeSH
- Glutamate Carboxypeptidase II metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Neoplasm Metastasis MeSH
- Prostatic Neoplasms * pathology surgery MeSH
- Positron-Emission Tomography * methods MeSH
- Prostatectomy * methods MeSH
- Prostate-Specific Antigen blood MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Geographicals
- Europe epidemiology MeSH
- Names of Substances
- Antigens, Surface MeSH
- Glutamate Carboxypeptidase II MeSH
- Prostate-Specific Antigen MeSH
BACKGROUND: De novo oligometastatic prostate cancer (omPCa) on prostate-specific membrane antigen (PSMA) positron emission tomography (PET) is a new disease entity and its optimal management remains unknown. OBJECTIVE: To analyze the outcomes of patients treated with cytoreductive radical prostatectomy (cRP) for omPCa on PSMA-PET. DESIGN, SETTING, AND PARTICIPANTS: Overall, 116 patients treated with cRP at 13 European centers were identified. Oligometastatic PCa was defined as miM1a and/or miM1b with five or fewer osseous metastases and/or miM1c with three or fewer lung lesions on PSMA-PET. INTERVENTION: Cytoreductive radical prostatectomy. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Thirty-day complications according to Clavien-Dindo, continence rates, time to castration-resistant PCa (CRPC), and overall survival (OS) were analyzed. RESULTS AND LIMITATIONS: Overall, 95 (82%) patients had miM1b, 18 (16%) miM1a, and three (2.6%) miM1c omPCa. The median prebiopsy prostate-specific antigen was 14 ng/ml, and 102 (88%) men had biopsy grade group ≥3 PCa. The median number of metastases on PSMA-PET was 2; 38 (33%), 29 (25%), and 49 (42%) patients had one, two, and three or more distant positive lesions. A total of 70 (60%) men received neoadjuvant systemic therapy, and 37 (32%) underwent metastasis-directed therapy. Any and Clavien-Dindo grade ≥3 complications occurred in 36 (31%) and six (5%) patients, respectively. At a median follow-up of 27 mo, 19 (16%) patients developed CRPC and eight (7%) patients died. The 1-yr urinary continence rate was 82%. The 2-yr CRPC-free survival and OS were 85.8% (95% confidence interval [CI] 78.5-93.7%) and 98.9% (95% CI 96.8-100%), respectively. The limitations include retrospective design and short-term follow-up. CONCLUSIONS: Cytoreductive radical prostatectomy is a safe and feasible treatment option in patients with de novo omPCa on PSMA-PET. Despite overall favorable oncologic outcomes, some of these patients have a non-negligible risk of early progression and thus should be considered for multimodal therapy. PATIENT SUMMARY: We found that patients treated at expert centers with surgery for prostate cancer, with a limited number of metastases detected using novel molecular imaging, have favorable short-term survival, functional results, and acceptable rates of complications.
Department of Radiotherapy Holy Cross Cancer Center Kielce Poland
Department of Surgery Candiolo Cancer Institute FPO IRCCS Candiolo Turin Italy
Department of Surgery Oncology and Gastroenterology University of Padua Padua Italy
Department of Urology Città della Salute e della Scienza University of Turin Turin Italy
Department of Urology LMU Klinikum Ludwig Maximilians University Munich Munich Germany
Department of Urology Medical University of Vienna Vienna Austria
Department of Urology Skåne University Hospital Lund University Malmö Sweden
Department of Urology St Antonius Hospital Utrecht The Netherlands
Department of Urology University Hospitals Leuven Leuven Belgium
Division of Nuclear Medicine IEO European Institute of Oncology IRCCS Milan Italy
References provided by Crossref.org
Metastasis-directed therapy in oligometastatic prostate cancer