| Literature DB >> 27889880 |
Takuma Narita1, Takuya Koie2, Teppei Ookubo3, Koji Mitsuzuka3, Shintaro Narita4, Hayato Yamamoto1, Takamitsu Inoue4, Shingo Hatakeyama1, Sadafumi Kawamura5, Tatsuo Tochigi5, Tomonori Habuchi4, Yoichi Arai3, Chikara Ohyama1.
Abstract
The optimal treatment for high-risk prostate cancer (Pca) remains to be established. The current guidelines recommend extended pelvic lymph node dissection (e-PLND) for selected intermediate- and high-risk patients treated with RP. However, the indications, optimal extent, and therapeutic benefits of e-PLND remain unclear. The aim of this study was to assess whether e-PLND confers an oncological benefit for high-risk Pca compared to neoadjuvant luteinizing hormone-releasing hormone and estramustine (LHRH + EMP). The Michinoku Urological Cancer Study Group database contained the data of 2403 consecutive Pca patients treated with RP at four institutes between March 2000 and December 2014. In the e-PLND group, we identified 238 high-risk Pca patients who underwent RP and e-PLND, with lymphatic tissue removal around the obturator and the external iliac regions, and hypogastric lymph node dissection. The neoadjuvant therapy with limited PLND (l-PLND) group included 280 high-risk Pca patients who underwent RP and removal of the obturator node chain between September 2005 and June 2014 at Hirosaki University. The outcome measure was BRFS. The 5-year biochemical recurrence-free survival rates for the neoadjuvant therapy with l-PLND group and e-PLND group were 84.9 and 54.7%, respectively (P < 0.0001). The operative time was significantly longer in the e-PLND group compared to that of the neoadjuvant therapy with l-PLND group. Grade 3/4 surgery-related complications were not identified in both groups. Although the present study was not randomized, neoadjuvant LHRH + EMP therapy followed by RP might reduce the risk of biochemical recurrence.Entities:
Keywords: Extended lymph node dissection; High-risk prostate cancer; Neoadjuvant therapy; Prostatectomy
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Year: 2016 PMID: 27889880 DOI: 10.1007/s12032-016-0859-0
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064