N/A
N=2,384
Modeling Clinical Failure in Prostate Cancer Patients Based on a Two-stage Statistical Model
Prostate Cancer
Bottom Line
View on ClinicalTrials.gov: NCT03979079 ↗Enrolled (actual)
2,384
Serious AEs
—
Results posted
Dec 2020
Primary outcome: Primary: Number of Participants With Clinical Failure After Initiation of Radiotherapy — 315 Participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- external beam radiation therapy (Radiation)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Male
- Sponsor
- Institut Bergonié
- Primary completion
- Jan 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Clinical Failure After Initiation of Radiotherapy |
315 | — |
| SECONDARY Number of Participants With Initiation of Salvage Therapy After Radiotherapy |
267 | — |
Summary
Biomarker series can indicate disease progression and predict clinical endpoints. When a treatment is prescribed depending on the biomarker, confounding by indication might be introduced if the treatment modifies the marker profile and risk of failure.
The two-stage model fitted within a Bayesian Markov Chain Monte Carlo framework is particularly flexible to account for such data. Prostate-specific antigens in prostate cancer patients treated with external beam radiation therapy can be monitored. In the presence of rising prostate-specific antigens after external beam radiation therapy, salvage hormone therapy can be prescribed to reduce both the prostate-specific antigens concentration and the risk of clinical failure, an illustration of confounding by indication. The prognostic value of hormone therapy and prostate-specific antigens trajectory on the risk of failure based on a two-stage model within a Bayesian framework to assess the role of the prostate-specific antigens profile on clinical failure while accounting for a secondary treatment prescribed by indication. the aim of this research is to model prostate specific antigens using a hierarchical piecewise linear trajectory with a random changepoint. Residual prostate-specific antigens variability can be expressed as a function of prostate-specific antigens concentration. Covariates in the survival model can include : hormone therapy, baseline characteristics, and individual predictions of the prostate-specific antigens nadir and timing and prostate-specific antigens slopes before and after the nadir as provided by the longitudinal process.
Eligibility Criteria
Inclusion Criteria
- clinically localized prostate cancer
- Clinical stage T1 to T4
- Node and metastasis negative
- Treated with external beam radiation therapy (RT).
Exclusion Criteria
- Patients with baseline or planned hormonotherapy
Data sourced from ClinicalTrials.gov (NCT03979079). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.