Literature DB >> 31115124

Outcomes after a first and/or second salvage treatment in patients with oligometastatic prostate cancer recurrence detected by (18-F) choline PET-CT.

Alfonso Gomez-Iturriaga1, Francisco Casquero Ocio1, Piet Ost2, Iratxe Fernandez3, Emilia Rodeño3, Roberto Llarena4, Jorge Garcia-Olaverri4, Roberto Ortiz de Zarate1, Jon Cacicedo1, Alina Ahtamon1, Pedro Bilbao1.   

Abstract

OBJECTIVE: The primary objective of this study was to assess clinical outcomes in patients with oligometastatic prostate cancer recurrence after single or repeated salvage radiation treatment.
METHODS: Forty-nine consecutive prostate cancer patients diagnosed with oligometastatic recurrence on Ch-PET have been prospectively treated. Seven (23%) patients had castrate-resistant disease. Clinical outcomes were assessed using the Kaplan-Meier method. Potential prognostic factors were examined using univariate proportional hazards regression.
RESULTS: The treatments administered to the initial oligorecurrence sites were intensity-modulated radiotherapy (IMRT) ± ADT (26 patients; 53%) and stereotactic ablative radiotherapy (SABR) ± ADT (23 patients; 47%). With a median follow-up of 24 months (range 6-39), 24 patients developed a biochemical failure. Twenty out of the 24 relapsed patients underwent a second Ch-PET/CT. Seven patients presented poly-metastatic relapse and 10 oligometastatic diseases. Six of 10 patients with a second oligorecurrence were treated again with SABR. Overall, 102 lesions were treated. Local control was detected in 45 (91.8%) patients. No relevant (grade ≥ 2) toxicity was reported, and there was no grade 3 toxicity. On univariate analysis, none of the variables were significantly predicted for clinical disease-free survival. At last follow-up visit, 24 patients (40%) were free from biochemical failure and 37 (71%) patients were free from clinical disease. The 2-year OS and PCSS were 91.8% and 95.9% respectively.
CONCLUSION: Salvage IMRT or SBRT of oligometastatic prostate cancer recurrence is associated with a prolonged cDFS. This may result in a longer time to develop castrate-resistant disease and a longer time without systemic therapies.
© 2019 John Wiley & Sons Ltd.

Entities:  

Keywords:  SABR; choline PET; oligometastases; oligorecurrence; radiotherapy

Mesh:

Substances:

Year:  2019        PMID: 31115124     DOI: 10.1111/ecc.13093

Source DB:  PubMed          Journal:  Eur J Cancer Care (Engl)        ISSN: 0961-5423            Impact factor:   2.520


  5 in total

1.  Stereotactic body radiotherapy (SBRT) in metachronous oligometastatic prostate cancer: a systematic review and meta-analysis on the current prospective evidence.

Authors:  Michael Yan; Nikitha Moideen; Vanessa Freitas Bratti; Fabio Ynoe de Moraes
Journal:  Br J Radiol       Date:  2020-09-04       Impact factor: 3.039

2.  Oligometastatic Prostate Adenocarcinoma. Clinical-Pathologic Study of a Histologically Under-Recognized Prostate Cancer.

Authors:  Claudia Manini; Alba González; David Büchser; Jorge García-Olaverri; Arantza Urresola; Ana Ezquerro; Iratxe Fernández; Roberto Llarena; Iñaki Zabalza; Rafael Pulido; Arkaitz Carracedo; Alfonso Gómez-Iturriaga; José I López
Journal:  J Pers Med       Date:  2020-12-04

Review 3.  Local Therapies in Oligometastatic and Oligoprogressive Prostate Cancer.

Authors:  Matthew P Deek; Ryan M Phillips; Phuoc T Tran
Journal:  Semin Radiat Oncol       Date:  2021-07       Impact factor: 5.421

Review 4.  Oligometastatic and Oligoprogression Disease and Local Therapies in Prostate Cancer.

Authors:  Matthew P Deek; Phuoc T Tran
Journal:  Cancer J       Date:  2020 Mar/Apr       Impact factor: 2.074

5.  Efficacy of repeated PSMA PET-directed radiotherapy for oligorecurrent prostate cancer after initial curative therapy.

Authors:  Christoph Henkenberens; Ann-Kathrin Oehus; Thorsten Derlin; Frank Bengel; Tobias L Ross; Markus A Kuczyk; Stefan Janssen; Hans Christiansen; Christoph A J von Klot
Journal:  Strahlenther Onkol       Date:  2020-05-12       Impact factor: 3.621

  5 in total

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