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Analysis of risk factors for disease progression after salvage radiation therapy with androgen deprivation therapy in prostate cancer patients who have prostate-specific antigen persistence after radical prostatectomy.
Lee, Kyeonghyo; Kim, Dongchan; Nam, Jiho; Park, Dahl; Kim, Wontaek; Joo, Jihyeon; Jeon, Hosang; Ki, Yongkan; Kim, Donghyun.
Afiliação
  • Lee K; Department of Radiation Oncology, Pusan National University Hospital, Busan, Korea.
  • Kim D; Department of Radiation Oncology, Pusan National University Hospital, Busan, Korea.
  • Nam J; Department of Radiation Oncology, Pusan National University Hospital, Busan, Korea.
  • Park D; Department of Radiation Oncology, Pusan National University School of Medicine, Yangsan, Korea.
  • Kim W; Department of Radiation Oncology, Pusan National University Hospital, Busan, Korea.
  • Joo J; Department of Radiation Oncology, Pusan National University Hospital, Busan, Korea.
  • Jeon H; Department of Radiation Oncology, Pusan National University School of Medicine, Yangsan, Korea.
  • Ki Y; Department of Radiation Oncology, Pusan National University School of Medicine, Yangsan, Korea.
  • Kim D; Department of Radiation Oncology, Pusan National University Yangsan Hospital, Yangsan, Korea.
Radiat Oncol J ; 42(2): 124-129, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38946074
ABSTRACT

PURPOSE:

To assess risk factors of disease progression after salvage radiation therapy (SRT) with androgen deprivation therapy (ADT) in case of prostate-specific antigen (PSA) persistence after radical prostatectomy (RP). MATERIALS AND

METHODS:

We analyzed 57 patients who received SRT with ADT between 2013 and 2019 due to PSA persistence after RP. The endpoint was disease progression defined by biochemical recurrence or clinical recurrence. Age, Pre-RP PSA level, Gleason score, pathologic stage, presence of pelvic lymph node dissection, surgical margins, and PSA at 6-8 weeks after RP were analyzed as predictive factors for disease progression. Kaplan-Meier method and Cox regression models were used for data analysis.

RESULTS:

At a median follow-up of 38 months (interquartile range, 26-61), 17 patients had disease progression. Pathologic T stage (pT3b vs. pT3a or lower; hazard ratio [HR] = 9.20; p = 0.035) and PSA level at 6-8 weeks after RP (≥2.04 vs. <2.04 ng/mL; HR = 5.85; p = 0.002) were predictors of disease progression. The 5-year disease progression-free survival rate was 46.7% in pT3b group as compared to 92.9 % in pT3a or lower group, and 18.4% for PSA ≥2.04 ng/mL after RP as compared to 79.2% for PSA <2.04 ng/mL.

CONCLUSION:

Pathological T stage (pT3b) and post RP PSA ≥2.04 ng/mL are independent risk factors of disease progression after SRT with ADT in patients with PSA persistence after RP.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiat Oncol J Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiat Oncol J Ano de publicação: 2024 Tipo de documento: Article