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PSA decay during salvage radiotherapy for prostate cancer as a predictor of disease outcome - 5 year follow-up of a prospective observational study.
Gunnlaugsson, Adalsteinn; Kjellén, Elisabeth; Bratt, Ola; Ahlgren, Göran; Johannesson, Vilberg; Blom, René; Nilsson, Per.
Afiliación
  • Gunnlaugsson A; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, 221 85 Lund, Sweden.
  • Kjellén E; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, 221 85 Lund, Sweden.
  • Bratt O; Department of Urology, Sahlgrenska University Hospital, 41345 Gothenburg, Sweden.
  • Ahlgren G; Department of Urology and Surgery, Skåne University Hospital, 221 85 Lund, Sweden.
  • Johannesson V; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, 221 85 Lund, Sweden.
  • Blom R; Department of Surgery, Halmstad Hospital, 302 33 Halmstad, Sweden.
  • Nilsson P; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, 221 85 Lund, Sweden.
Clin Transl Radiat Oncol ; 24: 23-28, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32613088
ABSTRACT
BACKGROUND AND

PURPOSE:

Biochemical recurrence after prostatectomy is commonly treated with salvage radiotherapy (SRT). In this prospective observational study we investigated the PSA decay rate, determined by predefined serial PSA measurements during SRT, as a predictor for treatment outcome. MATERIALS AND

METHODS:

Between 2013 and 2016, 214 patients were included in the study. The prescribed dose to the prostate bed was 70 Gy in 35 fractions (7 weeks) without hormonal treatment. PSA was measured weekly during SRT. Assuming first order kinetics, a PSA decay-rate constant (k) was calculated for 196 eligible patients. The ability of k to predict disease progression was compared with known clinical prediction parameters using Cox regression, logistic regression and ROC analyses. Disease progression was defined as continuously rising PSA after SRT, PSA increase by ≥0.2 ng/ml above nadir after SRT, hormonal treatment or clinical progression.

RESULTS:

After a median follow up of 4.7 years the estimated failure-free survival at 5 years was 56%. The PSA decay-rate constant (k) was found to be the strongest predictor of disease progression in both uni-and multivariable analyses.

CONCLUSION:

The addition of k to established clinical variables significantly improves the possibility to predict treatment outcome after SRT and could be used to personalize future therapies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Transl Radiat Oncol Año: 2020 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Transl Radiat Oncol Año: 2020 Tipo del documento: Article País de afiliación: Suecia
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