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  • Wiley  (2)
  • Iwamura, Masatsugu  (2)
  • 1
    In: The Prostate, Wiley, Vol. 77, No. 15 ( 2017-11), p. 1520-1527
    Abstract: We evaluated a five‐tiered Gleason grade groups arising from the 2014 International Society of Urological Pathology consensus conference on prognostic prediction in clinical stage T3a (extracapsular invasion) and T3b (seminal vesicle involvement) prostate cancer undergoing high‐dose‐rate brachytherapy (HDR‐BT). Methods From November 2003 to December 2012, 283 patients with stage T3 prostate cancer received HDR‐BT and external beam radiation therapy (EBRT) with long‐term androgen deprivation therapy (ADT). Of these, 203 (72%) and 80 (28%) patients had stage T3a and T3b disease, respectively. The mean dose to 90% of the planning target volume was 7.5 Gy/fraction of HDR‐BT. After five fractions, EBRT with 10 fractions of 3 Gy was administered. All patients first underwent ≥6 months of neoadjuvant ADT, and adjuvant ADT continued for 36 months. Median follow‐up was 74 months from the start of radiotherapy. Results The 10‐year biochemical recurrence (BCR) −free rate for stage T3a and T3b disease was 79% and 64%, respectively ( P  = 0.0083). The 10‐year cancer‐specific survival (CSS) rate for stage T3a and T3b was 96% and 91%, respectively ( P  = 0.0305). Although grade groups ≥4 were independent predictors for BCR in cT3a patients ( P  = 0.0270), they failed to significantly predict prostate cancer‐specific mortality (PCSM) among cT3a patients. Among cT3b patients, grade group 5 was a significant predictor of both BCR ( P  = 0.0017) and PCSM ( P  = 0.0233). Among stage T3a patients, no significant difference existed in 10‐year CSS between grade groups 5 and 4 (94% vs 97%, P  = 0.3960). In contrast, grade group 5 had a significantly worse outcome in 10‐year CSS than grade group 4 among stage T3b patients (74% vs 100%, P  = 0.0350). Conclusions Stage T3a patients with grade groups 4/5 and stage T3b with grade group 4 had fairly low PCSM risk. Approximately one of four patients among stage T3b patients with grade group 5 showed PCSM after combined HDR‐BT and EBRT with long‐term ADT. Stage T3b patients with grade group 5 may have a greater risk for PCSM.
    Type of Medium: Online Resource
    ISSN: 0270-4137 , 1097-0045
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 1494709-2
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  • 2
    In: The Prostate, Wiley, Vol. 79, No. 5 ( 2019-04), p. 506-514
    Abstract: Systemic Therapy in Advancing or Metastatic Prostate Cancer: Evaluation of Drug Efficacy (STAMPEDE) trial showed the survival benefit for prostate radiotherapy in newly diagnosed prostate cancer patients with a low metastatic burden. The result raises the next question whether additional radiotherapy to metastatic sites could improve the survival in those with a low metastatic burden. Methods We evaluated the efficacy and safety of prostate‐directed radiotherapy (PDRT) with or without metastasis‐directed radiotherapy (MDRT) in newly diagnosed oligometastatic patients who underwent combination of high‐dose‐rate prostate brachytherapy, external beam radiotherapy, and androgen deprivation therapy. Forty patients with bone metastasis and node positive prostate cancer were retrospectively analyzed. Of these, 22 (55%), 3 (7%), and 15 (38%) patients had N1M0, M1a, and M1b, respectively. Eighteen patients (45%) received MDRT to all metastatic sites. All patients initially underwent ≧6 months of androgen deprivation therapy. Oligometastatic disease was defined as presence of five or fewer metastatic lesions. Median follow‐up period was 62.5 months. Results Of the 40 patients, the 5‐year castration‐resistant prostate cancer (CRPC)‐free survival rate and cancer‐specific survival was 64.4% and 87.9%, respectively. Pre‐ or post‐treatment predictive value including prostate‐specific antigen (PSA) at diagnosis ≥20 ng/mL, Gleason grade group 5, positive biopsy core rate ≥51%, PSA nadir level of ≥0.02 ng/mL after the radiotherapy, and no MDRT were significantly associated with progression to CRPC. Patients with MDRT had significantly higher probability of achieving a PSA level of 〈 0.02 ng/mL than those without the therapy (88.8% vs 54.5%, P  = 0.0354) and consequently had a better CRPC‐free survival than those without the therapy (HR 0.319, 95%CI: 0.116‐0.877). Comparing PDRT alone, PDRT with MDRT did not significantly increase the incidences of genitourinary and gastrointestinal toxicities. Conclusions This single‐institutional study revealed the feasibility of combining prostate brachytherapy and MDRT for newly diagnosed oligometastatic prostate cancer. This combined approach has potential to prolong CRPC‐free survival.
    Type of Medium: Online Resource
    ISSN: 0270-4137 , 1097-0045
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 1494709-2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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