TY - JOUR
T1 - Radical Prostatectomy With and Without Neoadjuvant Chemohormonal Pretreatment for High-Risk Localized Prostate Cancer
T2 - A Comparative Propensity Score Matched Analysis
AU - Narita, Shintaro
AU - Nara, Taketoshi
AU - Kanda, Sohei
AU - Numakura, Kazuyuki
AU - Saito, Mitsuru
AU - Inoue, Takamitsu
AU - Satoh, Shigeru
AU - Nanjo, Hiroshi
AU - Tsuchiya, Norihiko
AU - Mitsuzuka, Koji
AU - Koie, Takuya
AU - Kawamura, Sadafumi
AU - Ohyama, Chikara
AU - Tochigi, Tatsuo
AU - Arai, Yoichi
AU - Habuchi, Tomonori
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/2
Y1 - 2019/2
N2 - Background: To investigate the clinical outcomes in patients with high-risk prostate cancer (PCa) treated with neoadjuvant chemohormonal therapy (NCHT) before radical prostatectomy (RP). Patients and Methods: Our NCHT protocol involved complete androgen blockade followed by 6 cycles of docetaxel (30 mg/m 2 ) plus estramustine phosphate (560 mg). NCHT was provided to 60 patients with PCa before RP, and we compared the clinical and pathologic outcomes with those of 349 patients with high-risk PCa who underwent RP alone using propensity score matching. The data for those who underwent RP alone were obtained from the Michinoku Japan Urological Cancer Study Group database. Results: In the NCHT group, 10.0% experienced pathologic complete response, 3.3% had positive surgical margins, and 13.3% developed severe complications (Clavien-Dindo grade III or higher) after RP. The median follow-up duration was 42.5 months, and the 5-year biochemical recurrence (BCR)-free survival was 60.1%. In multivariate analysis, pN+ was an independent prognostic factor for BCR (hazard ratio = 5.251, 95%CI 1.300-21.201; P =.020). In propensity score matching, the BCR rate in the NCHT group was significantly lower than that in the RP alone group (P =.021). In subgroup analyses, the BCR rate in patients with a single high-risk factor was significantly lower in the NCHT group than in the RP-alone group (P =.027). Conclusion: NCHT before RP can reduce the risk of BCR in patients with high-risk PCa, particularly if a single high-risk factor is present. However, the potential for perioperative complications should be considered.
AB - Background: To investigate the clinical outcomes in patients with high-risk prostate cancer (PCa) treated with neoadjuvant chemohormonal therapy (NCHT) before radical prostatectomy (RP). Patients and Methods: Our NCHT protocol involved complete androgen blockade followed by 6 cycles of docetaxel (30 mg/m 2 ) plus estramustine phosphate (560 mg). NCHT was provided to 60 patients with PCa before RP, and we compared the clinical and pathologic outcomes with those of 349 patients with high-risk PCa who underwent RP alone using propensity score matching. The data for those who underwent RP alone were obtained from the Michinoku Japan Urological Cancer Study Group database. Results: In the NCHT group, 10.0% experienced pathologic complete response, 3.3% had positive surgical margins, and 13.3% developed severe complications (Clavien-Dindo grade III or higher) after RP. The median follow-up duration was 42.5 months, and the 5-year biochemical recurrence (BCR)-free survival was 60.1%. In multivariate analysis, pN+ was an independent prognostic factor for BCR (hazard ratio = 5.251, 95%CI 1.300-21.201; P =.020). In propensity score matching, the BCR rate in the NCHT group was significantly lower than that in the RP alone group (P =.021). In subgroup analyses, the BCR rate in patients with a single high-risk factor was significantly lower in the NCHT group than in the RP-alone group (P =.027). Conclusion: NCHT before RP can reduce the risk of BCR in patients with high-risk PCa, particularly if a single high-risk factor is present. However, the potential for perioperative complications should be considered.
KW - Combined androgen blockade
KW - Docetaxel
KW - Estramustine phosphate
KW - Neoadjuvant chemotherapy
KW - Prostatectomy
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U2 - 10.1016/j.clgc.2018.09.019
DO - 10.1016/j.clgc.2018.09.019
M3 - Article
C2 - 30391137
AN - SCOPUS:85055738003
SN - 1558-7673
VL - 17
SP - e113-e122
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 1
ER -