Correlation of Prostate-specific Antigen Kinetics with Overall Survival and Radiological Progression-free Survival in Metastatic Castration-sensitive Prostate Cancer Treated with Abiraterone Acetate plus Prednisone or Placebos Added to Androgen Deprivation Therapy: Post Hoc Analysis of Phase 3 LATITUDE Study

被引:92
作者
Matsubara, Nobuaki [1 ]
Chi, Kim N. [2 ]
Ozguroglu, Mustafa [3 ]
Rodriguez-Antolin, Alfredo [4 ]
Feyerabend, Susan [5 ]
Fein, Luis [6 ]
Alekseev, Boris Y. [7 ]
Sulur, Giri [8 ]
Protheroe, Andrew [9 ]
Li, Susan [10 ]
Mundle, Suneel [11 ]
De Porre, Peter [12 ]
Tran, Namphuong [8 ]
Fizazi, Karim [13 ]
机构
[1] Natl Canc Ctr Hosp East, Chiba, Japan
[2] BC Canc Agcy, Vancouver, BC, Canada
[3] Istanbul Univ Cerrahpasa, Cerrahpa Med Fac, Istanbul, Turkey
[4] 12 Octubre Univ Hosp, Madrid, Spain
[5] Studienpraxis Urol, Nurtingen, Germany
[6] Inst Oncol Rosario, Rosario, Argentina
[7] PA Hertsen Moscow Canc Res Inst, Moscow, Russia
[8] Janssen Res & Dev, Los Angeles, CA USA
[9] Oxford Univ Hosp Fdn NHS Trust, Oxford, England
[10] Janssen Res & Dev, Spring House, PA USA
[11] Janssen Res & Dev, Raritan, NJ USA
[12] Janssen Res & Dev, Beerse, Belgium
[13] Univ Paris Sud, Inst Gustave Roussy, Villejuif, France
关键词
Abiraterone; Metastatic castration-sensitive prostate cancer; Overall survival; Prostate-specific antigen kinetics; Radiological progression-free survival; CLINICAL-TRIALS; DOCETAXEL; PREDICTS; RECOMMENDATIONS; SURROGACY; LEVEL; TIME; PSA;
D O I
10.1016/j.eururo.2019.11.021
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: LATITUDE, a randomized, double-blind trial, compared abiraterone acetate and prednisone (AAP) + androgen deprivation therapy (ADT) versus placebo (PBO) + ADT in high-risk metastatic castration-sensitive prostate cancer (mCSPC). Objective: To assess the correlation of prostate-specific antigen (PSA) kinetics with overall survival (OS) and radiological progression-free survival (rPFS). Design, setting, and participants: A post hoc analysis of data from 597 men receiving AAP + ADT and 602 receiving PBO + ADT. Outcome measurements and statistical analysis: The associations of PSA-related outcomes (rates of confirmed 50% [PSA50] and 90% [PSA90] decline from baseline PSA [Prostate Cancer Working Group 2 criteria], rates of PSA < 0.2 ng/ml, median nadir PSA, time to PSA nadir [TPN], and time to PSA progression [TPP] with long-term outcomes [OS and rPFS]) were evaluated. Hazard ratios (HRs) were estimated using Cox proportional hazard model. Correlations of TPP with coprimary endpoints rPFS and OS were evaluated using Kendall's tau (KT). Results and limitations: AAP + ADT significantly delayed median TPP versus PBO + ADT (33.2 vs 7.4 mo; HR: 0.3, p < 0.001). TPP correlated with rPFS (KT = 0.921) and OS (KT = 0.666). In the AAP + ADT group, 91% had PSA50 and 79% had PSA90 responses (relative risk [RR]: 1.36 and 2.30, respectively; p < 0.001 for both comparisons vs PBO + ADT). Compared with nonresponders, PSA50 and PSA90 responders had reduced risk of death (RR: 0.44 and 0.12, respectively). At 6 mo, 40% receiving AAP + ADT and 6.5% receiving PBO + ADT achieved PSA <0.1 ng/ml, which was significantly associated with longer rPFS and OS. Median nadir PSA was 0.09 ng/ml with AAP + ADT versus 2.36 ng/ml with PBO + ADT. Median TPN (AAP + ADT, 6.4 mo; PBO + ADT, 3.8 mo) positively correlated with rPFS and OS. Conclusions: Superior PSA response dynamics with AAP + ADT versus ADT + PBO strongly correlated with long-term outcomes of rPFS and OS in high-risk mCSPC. Patient summary: We found that low prostate-specific antigen levels (<0.1 ng/ml) after 6 mo may indicate a good long-term response to treatment. Our results need confirmation. (C) 2019 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:494 / 500
页数:7
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