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N/A N=2,384

Modeling Clinical Failure in Prostate Cancer Patients Based on a Two-stage Statistical Model

Prostate Cancer

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

OutcomeResultp-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
View full record on ClinicalTrials.gov →

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.

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