ST-DoxPCa (AI “virtual spatial transcriptomics”) identifies an OS-benefiting subgroup for adjuvant docetaxel in high-risk localized prostate cancer
- Cancer type
- Prostate Cancer
- Published in
- New in Oncology - June 25, 2026
ST-DoxPCa is an AI/computational pathology biomarker built from routine H&E biopsies using a Vision Transformer to infer spot-level expression for a prostate gene panel (distilled to a locked 26-gene signature; includes genes such as PTEN, NKX3-1, ACPP, FASN, TMPRSS2) and aggregate to patient-level risk features. In NRG/RTOG 0521 (Phase 3; high-risk localized prostate cancer treated with RT+long-term ADT ± adjuvant docetaxel; n=350, RT+ADT n=169 vs RT+ADT+DTX n=181), ST-DoxPCa-positive patients had a significant OS benefit from docetaxel (HR=0.38, 95% CI 0.18–0.83; p=0.012), while ST-DoxPCa-negative patients had no OS benefit (HR=1.05, 95% CI 0.67–1.63; p=0.84)—notably aligning with the parent trial’s “modest/limited” unselected benefit signal that attenuated with longer follow-up (i.e., adding docetaxel to RT+ADT has not been a universally durable OS win in the full population).
Take home
If this locked, biopsy-based signature holds up in additional cohorts, it’s exactly the kind of “treat-more vs treat-less” classifier that could keep docetaxel for the subset that actually lives longer with intensification—while sparing the biomarker-negative majority the toxicity and inconvenience of chemo with no OS upside.
Source: Read the original publication
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