Adverse pathology as a predictor of distant metastasis and prostate cancer mortality with 20-year follow up.

Authors

null

Michael Austin Brooks

Harris Health/Ben Taub Hospital, Baylor College of Medicine and Dan L. Duncan Comprehensive Cancer Center, Houston, TX

Michael Austin Brooks , Lewis Thomas , Cristina Magi-Galluzi , Jianbo Li , Michael Crager , Ruixiao Lu , John Abran , Tamer Aboushwareb , Eric A. Klein

Organizations

Harris Health/Ben Taub Hospital, Baylor College of Medicine and Dan L. Duncan Comprehensive Cancer Center, Houston, TX, Cleveland Clinic Foundation, Cleveland, OH, Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, Genomic Health Inc, an Exact Sciences Corporation, Redwood City, CA

Research Funding

Pharmaceutical/Biotech Company
Genomic Health Incorporated, an Exact Sciences corporation.

Background: Adverse pathology (AP) at radical prostatectomy (RP) is often used as a proxy for long-term prostate cancer outcomes. The goal of this study was to assess the association of AP at RP, defined as high-grade (> Grade Group 3) and/or non-organ confined disease (pT3), with distant metastasis and prostate cancer death. Methods: A stratified cohort sample of 428 patients was used to evaluate the association of adverse pathology with the risk of distant metastases and prostate cancer-specific mortality over 20 years after prostatectomy in 2641 patients treated between 1987-2004. Cox regression of cause-specific hazards was used to estimate the absolute risk of both endpoints, with death from other causes treated as a competing risk. Subgroup analysis in patients with low/intermediate risk disease potentially eligible for active surveillance was performed. Results: Among the 428 patients, 343 had AUA Low or Intermediate risk disease and 85 had High risk disease. Median follow-up time was 15.5 years (IQR 14.6–16.6 years). Using the cohort sampling weights for estimation, at RP 29.8% of patients had high-grade disease, 42.3 % had non-organ confined disease, 19.3% had both, and thus 52.8% had AP. Adverse pathology was highly associated with metastasis and prostate cancer mortality in the overall cohort (HR 12.30, 95% CI 5.30-28.55, and 10.03, 95% CI 3.42-29.47, respectively, both p<0.001), and in the low/intermediate risk subgroup potentially eligible for active surveillance (HR 10.48, 95% CI 4.18-26.28, and 8.60, 95% CI 2.40-30.84, respectively, both p≤0.001). Conclusions: Adverse pathology at radical prostatectomy is highly associated with future development of metastasis and prostate cancer mortality and may be used as a short-term predictor of outcomes.

Cox proportional hazards regression effect of AP and estimated absolute risk of distant metastasis and prostate cancer specific mortality.

Event20-year absolutea risk of event (95% CI)
Hazard ratio (95% CI) for APAbsence of APPresence of AP
All patients (n=428)
Distant metastasis12.30 (5.30, 28.55)1.5% (0.7%, 3.5%)16.9% (13.2%, 21.4%)
(105 events)p<.001
Prostate cancer mortality10.03 (3.42, 29.47)0.6% (0.2%, 1.7%)5.8% (4.2%, 7.9%)
(53 events)p<.001
Low and Intermediate Risk patients (n = 343)
Distant metastasis10.48 (4.18, 26.28)1.5% (0.6%, 3.6%)13.9% (10.2%, 18.9%)
(67 events)p<.001
Prostate cancer mortality8.60 (2.40, 30.84)0.5% (0.1%, 1.6%)4.0% (2.6%, 6.2%)
(30 events)p=.001

aAbsolute risk treating death due to non-prostate-cancer causes as a competing risk. AP=adverse pathology; CI = confidence interval

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Abstract Details

Meeting

2021 Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session: Prostate Cancer - Localized Disease

Track

Prostate Cancer - Localized

Sub Track

Patient-Reported Outcomes and Real-World Evidence

Citation

J Clin Oncol 39, 2021 (suppl 6; abstr 219)

DOI

10.1200/JCO.2021.39.6_suppl.219

Abstract #

219

Poster Bd #

Online Only

Abstract Disclosures

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