MISC

査読有り 国際誌
2019年4月

Dose escalation of external beam radiotherapy for high-risk prostate cancer-Impact of multiple high-risk factor.

Asian journal of urology
  • Rei Umezawa
  • Koji Inaba
  • Satoshi Nakamura
  • Akihisa Wakita
  • Hiroyuki Okamoto
  • Keisuke Tsuchida
  • Tairo Kashihara
  • Kazuma Kobayashi
  • Ken Harada
  • Kana Takahashi
  • Naoya Murakami
  • Yoshinori Ito
  • Hiroshi Igaki
  • Keiichi Jingu
  • Jun Itami
  • 全て表示

6
2
開始ページ
192
終了ページ
199
記述言語
英語
掲載種別
DOI
10.1016/j.ajur.2017.07.002

Objective: To retrospectively investigate the treatment outcomes of external beam radiotherapy with androgen deprivation therapy (ADT) in high-risk prostate cancer in three radiotherapy dose groups. Methods: Between 1998 and 2013, patients with high-risk prostate cancer underwent three-dimensional conformal radiotherapy or intensity-modulated radiotherapy of 66 Gy, 72 Gy, or 78 Gy with ADT. Prostate-specific antigen (PSA) relapse was defined using the Phoenix definition. PSA relapse-free survival (PRFS) was evaluated in each radiotherapy dose group. Moreover, high-risk patients were divided into H-1 (patients with multiple high-risk factors) and H-2 (patients with a single high-risk factor) as risk subgroups. Results: Two hundred and eighty-nine patients with a median follow-up period of 77.3 months were analyzed in this study. The median duration of ADT was 10.1 months. Age, Gleason score, T stage, and radiotherapy dose influenced PRFS with statistical significance both in univariate and multivariate analyses. The 4-year PRFS rates in Group-66 Gy, Group-72 Gy and Group-78 Gy were 72.7%, 81.6% and 90.3%, respectively. PRFS rates in the H-1 subgroup differed with statistical significance with an increasing radiotherapy dose having a more favorable PRFS, while PRFS rates in H-2 subgroup did not differ with increase in radiotherapy dose. Conclusion: Dose escalation for high-risk prostate cancer in combination with ADT improved PRFS. PRFS for patients in the H-1 subgroup was poor, but dose escalation in those patients was beneficial, while dose escalation in the H-2 subgroup was not proven to be effective for improving PRFS.

リンク情報
DOI
https://doi.org/10.1016/j.ajur.2017.07.002
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31061806
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488684
ID情報
  • DOI : 10.1016/j.ajur.2017.07.002
  • PubMed ID : 31061806
  • PubMed Central 記事ID : PMC6488684

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