Validation of the Decipher Genomic Classifier in Patients receiving Salvage Radiotherapy without Hormone Therapy after Radical Prostatectomy – An Ancillary Study of the SAKK 09/10 Randomized Clinical Trial (2022, Full Text)
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Highlights• Decipher identifies patients at highest risk of progression who may require treatment intensification
• Decipher defines subgroups associated with improved outcomes when treated with very early SRT compared to late SRT
• Transcript
omic profiling can guide personalized management of SRT timing and the addition of systemic therapy
Abstract
BackgroundThe Decipher genomic classifier (
GC) has shown to independently prognosticate outcomes in prostate cancer. The objective of this study was to validate the GC in a randomized phase 3 trial of dose-escalated salvage radiotherapy (SRT) after radical prostatectomy.
Patients and MethodsA clinical grade whole-transcript
ome assay was performed on RP samples obtained from patients enrolled in SAKK 09/10, a phase 3 trial of 350 men with biochemical recurrence post-radical prostatectomy randomized to 64Gy vs. 70Gy without concurrent hormonal therapy or pelvic nodal radiotherapy (RT). A pre-specified statistical plan was developed to assess the impact of the GC on clinical outcomes. The primary endpoint was biochemical progression; secondary endpoints were clinical progression and time to hormone therapy. Multivariable analyses adjusted for age, T-category, Gleason score, post-radical prostatectomy persistent prostate-specific antigen (PSA), PSA at randomization, and randomization arm were conducted, accounting for competing risks.
ResultsThe analytic cohort of 226 patients was representative of the overall trial, with median follow-up of 6.3 years (IQR 6.1-7.2). GC (high vs. low-intermediate) was independently associated with biochemical progression (subdistribution hazard ratio [sHR] 2.26 [95% CI 1.42-3.60], p<0.001), clinical progression (HR 2.29 [95% CI 1.32-3.98], p=0.003), and use of hormone therapy (sHR 2.99 [95% CI 1.55-5.76], p=0.001). GC high patients had 5-year freedom from biochemical progression of 45% vs. 71% for GC low-intermediate. Dose escalation did not benefit the overall cohort, nor patients with lower vs. higher GC scores.
ConclusionsThis study represents the first contemporary randomized controlled trial in patients treated with early SRT without concurrent hormone therapy or pelvic nodal RT that has validated the prognostic utility of the GC. Independent of standard clinicopathologic variables and RT dose, high-GC patients were more than twice as likely than lower-GC patients to experience biochemical and clinical progression and receive of salvage hormone therapy. This data confirms the clinical value of Decipher GC to personalize the use of concurrent systemic therapy in the postoperative salvage setting."
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The paper defines the SRT timing categories according to PSA:
"Routine treatment decisions made for men post-radical prostatectomy include the use of
very early SRT (<0.2 ng/mL), early SRT (0.2-0.5 ng/mL), or late SRT (>0.5 ng/mL)."
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We now have both PSMA PET/CT imaging and a clinically validated genomic classifier to help with the difficult decisions whether to add ADT and/or pelvic node RT to salvage prostate fossa irradiation. The trend in the past couple of years has been away from adjuvant and towards salvage therapy to avoid overtreatment (for intermediate-risk, post-RP men with adverse pathologies), and we may see something similar with regard to customizing SRT for BCR (+/-ADT, +/- pelvic node irradiation, SRT timing), again to avoid overtreatment.
Djin