Postradical prostatectomy prostate-specific antigen outcomes after 6 versus 18 months of perioperative androgen-deprivation therapy in men with localized, unfavorable intermediate-risk or high-risk prostate cancer: Results of part 2 of a randomized phase 2 trial

被引:5
作者
Mckay, Rana R. [1 ,2 ]
Xie, Wanling [3 ]
Yang, Xiaoyu [4 ]
Acosta, Andres [5 ]
Rathkopf, Dana [6 ]
Laudone, Vincent P. [7 ]
Bubley, Glenn J. [3 ]
Einstein, David J. [8 ]
Chang, Peter [9 ]
Wagner, Andrew A. [9 ]
Kane, Christopher J. [2 ]
Preston, Mark A. [10 ]
Kilbridge, Kerry [4 ]
Chang, Steven L. [10 ]
Choudhury, Atish D. [4 ]
Pomerantz, Mark M. [4 ]
Trinh, Quoc-Dien [10 ]
Kibel, Adam S. [10 ]
Taplin, Mary-Ellen [4 ,11 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA USA
[2] Univ Calif San Diego, Dept Urol, La Jolla, CA USA
[3] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[5] Brigham & Womens Hosp, Dept Pathol, Boston, MA USA
[6] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[7] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY USA
[8] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA USA
[9] Beth Israel Deaconess Med Ctr, Dept Surg, Boston, MA USA
[10] Brigham & Womens Hosp, Dept Surg, Boston, MA USA
[11] Dana Farber Canc Ctr, Dept Med, 450 Brookline Ave, Boston, MA 02215 USA
关键词
androgen-deprivation therapy; biochemical recurrence; high-risk; neoadjuvant hormone therapy; pathologic response; prostate cancer; radical prostatectomy; ABIRATERONE; ENZALUTAMIDE; LEUPROLIDE; SURVIVAL; ACETATE;
D O I
10.1002/cncr.35170
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Patients with localized, unfavorable intermediate-risk and high-risk prostate cancer have an increased risk of relapse after radical prostatectomy (RP). The authors previously reported on part 1 of this phase 2 trial testing neoadjuvant apalutamide, abiraterone, prednisone, plus leuprolide (AAPL) or abiraterone, prednisone, and leuprolide (APL) for 6 months followed by RP. The results demonstrated favorable pathologic responses (tumor <5 mm) in 20.3% of patients (n = 24 of 118). Herein, the authors report the results of part 2.Methods: For part 2, patients were randomized 1:1 to receive either AAPL for 12 months (arm 2A) or observation (arm 2B), stratified by neoadjuvant therapy and pathologic tumor classification. The primary end point was 3-year biochemical progression-free survival. Secondary end points included safety and testosterone recovery (>200 ng/dL).Results: Overall, 82 of 118 patients (69%) enrolled in part 1 were randomized to part 2. A higher proportion of patients who were not randomized to adjuvant therapy had a favorable prostatectomy pathologic response (32.3% in nonrandomized patients compared with 17.1% in randomized patients). In the intent-to-treat analysis, the 3-year biochemical progression-free survival rate was 81% for arm 2A and 72% for arm 2B (hazard ratio, 0.81; 90% confidence interval, 0.43-1.49). Of the randomized patients, 81% had testosterone recovery in the AAPL group compared with 95% in the observation group, with a median time to recovery of <12 months in both arms.Conclusions: In this study, because 30% of patients declined adjuvant treatment, part B was underpowered to detect differences between arms. Future perioperative studies should be biomarker-directed and include strategies for investigator and patient engagement to ensure compliance with protocol procedures.
引用
收藏
页码:1629 / 1641
页数:13
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