{Reference Type}: Journal Article
{Title}: A randomised trial of short- vs long-term androgen deprivation with salvage radiotherapy for biochemical failure following radical prostatectomy: URONCOR 06-24.
{Author}: González-San Segundo C;López Campos F;Gómez Iturriaga A;Rodríguez A;Olivera J;Duque-Santana V;Sancho G;Henríquez I;Conde AJ;Valero J;Maldonado X;Glaria L;Caballero B;Sanmamed N;Mases J;Boladeras-Inglada AM;Montijano M;Santos M;Álvarez A;Martínez JI;Couñago F;
{Journal}: BJU Int
{Volume}: 0
{Issue}: 0
{Year}: 2024 07 23
{Factor}: 5.969
{DOI}: 10.1111/bju.16484
{Abstract}: Salvage radiotherapy (SRT) and androgen-deprivation therapy (ADT) are widely used in routine clinical practice to treat patients with prostate cancer who develop biochemical recurrence (BCR) after radical prostatectomy (RP). However, there is no standard-of-care consensus on optimal duration ADT. Investigators propose three distinct risk groups in patients with prostate cancer treated with SRT in order to better define the indications and duration of ADT combined with SRT.<BR>The URONCOR 06-24 trial (ClinicalTrials.gov identifier NCT05781217) is a prospective, multicentre, randomised, open-label, phase III, clinical trial. The aim of the trial is to determine the impact of short-term (6 months) vs long-term (24 months) ADT in combination with SRT on distant metastasis-free survival (MFS) in patients with prostate cancer with BCR after RP (intermediate and high risk).<BR>The primary endpoint is 5-year MFS rates in patients with prostate cancer treated with long- vs short-term ADT in combination with SRT. Secondary objectives are biochemical-relapse free interval, pelvic progression-free survival, time to start of systemic treatment, time to castration resistance, cancer-specific survival, overall survival, acute and late toxicity, and quality of life.<BR>Total of 534 patients will be randomised 1:1 to ADT 6 months or ADT 24 months with a luteinizing hormone-releasing hormone analogue in combination with SRT, stratified by risk group and pathological lymph node status.<BR>The study is conducted under the guiding principles of the World Medical Association Declaration of Helsinki. The results will be disseminated at research conferences and in peer-reviewed journals.<BR>EudraCT number 2021-006975-41.