Mode
Text Size
Log in / Sign up
Phase 3 Completed N=1,401 Randomized Quadruple-blind Treatment

Safety and Efficacy Study of Enzalutamide in Patients With Nonmetastatic Castration-Resistant Prostate Cancer

Nonmetastatic Castration-Resistant Prostate Cancer · Prostate Cancer · Cancer of the Prostate
Source: ClinicalTrials.gov NCT02003924 ↗
Enrolled (actual)
1,401
Serious AEs
32.7%
Results posted
Jul 2018
Primary outcomePrimary: Metastasis Free Survival (MFS) — 36.6; 14.7 months — p=<0.0001
◆ Published Evidence
Established
20citations · ~7 / year
Nadir Prostate-specific Antigen as an Independent Predictor of Survival Outcomes: A Post Hoc Analysis of the PROSPER Randomized Clinical Trial.
The Journal of urology · 2023 · Open access · Likely link

Summary

The purpose of this study is to assess the safety and efficacy of enzalutamide in patients with non metastatic prostate cancer.

Linked Publications (5)

  • Nadir Prostate-specific Antigen as an Independent Predictor of Survival Outcomes: A Post Hoc Analysis of the PROSPER Randomized Clinical Trial.
    The Journal of urology · 2023 · 20 citations · Open access · Likely link
  • US Population Reference Values for Health-Related Quality of Life Questionnaires Based on Demographics of Patients with Prostate Cancer.
    Advances in therapy · 2022 · 4 citations · Open access · Likely link
  • Radiographic Progression With and Without Prostate-Specific Antigen Rise in Patients With Advanced Prostate Cancer Treated With Enzalutamide.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026 · 1 citation · Open access · Likely link
  • From Androgen Deprivation to Precision Therapy: A Bibliometric Review of Global Research Trends (2008-2023).
    American journal of men's health · 2025 · 1 citation · Open access · Likely link
  • Which traits affect how long patients with advanced prostate cancer live when treated with enzalutamide?
    Future oncology (London, England) · 2022 · 0 citations · Open access · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Metastasis Free Survival (MFS)
36.6; 14.7 <0.0001 sig
SECONDARY
Time to Prostate-Specific Antigen (PSA) Progression
37.2; 3.9 <0.0001 sig
SECONDARY
Time to First Use of New Antineoplastic Therapy
39.6; 17.7 <0.0001 sig
SECONDARY
Overall Survival
67.0; 56.3 0.0011 sig
SECONDARY
Time to Pain Progression
18.5; 18.4 0.6534
SECONDARY
Time to First Use of Cytotoxic Chemotherapy
NA; 39.7 <0.0001 sig
SECONDARY
Chemotherapy-Free Disease Specific Survival
39.6; 38.9
SECONDARY
Chemotherapy-Free Survival
38.1; 34.0
SECONDARY
Percentage of Participants With Prostate Specific Antigen (PSA) Response
76.3; 2.4; 55.9; 0.4; 9.6; 0 <0.0001 sig
SECONDARY
Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Global Score
119.5; 120.8; -4.0; -3.0; -4.6; -3.5
SECONDARY
Number of Participants With European Quality of Life-5 Dimensions-5 Levels (EQ-5D-5L) Mobility Domain Score
578; 298; 183; 100; 100; 33
SECONDARY
Number of Participants With European Quality of Life-5 Dimensions-5 Levels (EQ-5D-5L) Self-Care Domain Score
805; 415; 51; 23; 22; 1
SECONDARY
Number of Participants With European Quality of Life-5 Dimensions-5 Levels (EQ-5D-5L) Usual Activities Domain Score
646; 356; 167; 64; 56; 14
SECONDARY
Number of Participants With European Quality of Life-5 Dimensions-5 Levels (EQ-5D-5L) Pain/Discomfort Domain Score
546; 292; 240; 117; 86; 25
SECONDARY
Number of Participants With European Quality of Life-5 Dimensions-5 Levels (EQ-5D-5L) Anxiety/ Depression Domain Score
595; 310; 231; 100; 51; 24
SECONDARY
European Quality of Life-5 Dimensions-5 Levels (EQ-5D-5L) Overall Health Status Visual Analog Score (VAS)
76.2; 77.5; 74.7; 74.9; 74.6; 74.0
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 31
285; 162; 348; 160; 207; 92
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 32
193; 108; 423; 195; 200; 103
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 33
406; 197; 266; 147; 150; 70
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 34
479; 235; 273; 146; 93; 40
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 35
646; 330; 177; 84; 45; 18
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 36
550; 283; 273; 124; 36; 20
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 37
775; 380; 92; 47; 10; 8
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 38
83; 37; 40; 19; 15; 3
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 39
666; 338; 173; 80; 35; 11
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 40
758; 393; 112; 40; 9; 4
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 41
794; 404; 78; 32; 11; 2
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 42
836; 422; 48; 17; 0; 0
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 43
667; 320; 190; 103; 22; 16
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 44
374; 177; 314; 166; 151; 68
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 45
688; 333; 146; 80; 38; 24
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 46
663; 323; 189; 89; 22; 22
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 47
820; 399; 48; 25; 10; 10
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 48
677; 315; 153; 95; 40; 16
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 49
435; 214; 234; 131; 138; 59
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 50
586; 291; 204; 101; 67; 32
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 51
735; 374; 98; 38; 41; 19
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 52
5; 6; 23; 11; 14; 5
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 53
6; 4; 19; 5; 4; 4
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 54
11; 7; 14; 4; 3; 2
SECONDARY
Number of Participants With European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-Prostate 25 (QLQ-PR25) Module Score for Question 55
31; 13; 13; 8; 4; 0
SECONDARY
Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)
808; 360; 226; 85
SECONDARY
Number of Participants With Treatment-Emergent Adverse Events Greater Than or Equal to Grade 3, Based on National Cancer Institute (NCI) Common Terminology Criteria (CTC) for AEs (CTCAE), Version 4.0
292; 109
SECONDARY
Number of Participants With Discontinuations From Study Treatment Due to Adverse Events (AEs)
87; 28
SECONDARY
Number of Participants With Increase of 2 or More National Cancer Institute Common Terminology Criteria for Adverse Event (NCI CTCAE) (Version 4.0) Toxicity Grades Above Baseline - Hematology
12; 7; 7; 7; 4; 2
SECONDARY
Number of Participants With Increase of 2 or More National Cancer Institute Common Terminology Criteria for Adverse Event (NCI CTCAE) (Version 4.0) Toxicity Grades Above Baseline - Chemistry
4; 1; 7; 0; 3; 6
SECONDARY
Number of Participants With Clinically Significant Vital Signs
738; 328; 563; 229; 7; 4

Eligibility Criteria

Inclusion Criteria

  • Histologically or cytologically confirmed adenocarcinoma of the prostate without neuroendocrine differentiation, signet cell, or small cell features;
  • Ongoing androgen deprivation therapy with a gonadotropin-releasing hormone (GnRH) agonist/antagonist or prior bilateral orchiectomy (medical or surgical castration);
  • Testosterone ≤ 50 ng/dL (≤ 1.73 nmol/L) at screening;
  • Progressive disease on androgen deprivation therapy at enrollment;
  • PSA and the screening PSA assessed by the central laboratory (central PSA) should be ≥ 2 µg/L (2 ng/mL:
  • PSA doubling time ≤ 10 months;
  • No prior or present evidence of metastatic disease;
  • Asymptomatic prostate cancer;
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
  • Estimated life expectancy ≥ 12 months.

Exclusion Criteria

  • Prior cytotoxic chemotherapy;
  • Use of hormonal therapy or biologic therapy for prostate cancer (other than approved bone targeting agents and GnRH agonist/antagonist therapy) or use of an investigational agent within 4 weeks of randomization;
  • Known or suspected brain metastasis or active leptomeningeal disease;
  • History of another invasive cancer within 3 years of randomization;
  • Absolute neutrophil count 2 mg/dL (177 µmol/L) at screening;
  • Albumin < 3.0 g/dL (30 g/L) at screening;
  • History of seizure or any condition that may predispose to seizure;
  • Clinically significant cardiovascular disease;
  • Gastrointestinal disorder affecting absorption;
  • Major surgery within 4 weeks of randomization;
  • Hypersensitivity reaction to the active pharmaceutical ingredient or any of the capsule components, including Labrasol, butylated hydroxyanisole, and butylated hydroxytoluene;
  • Any concurrent disease, infection, or comorbid condition that interferes with the ability of the patient to participate in the trial, which places the patient at undue risk, or complicates the interpretation of data, in the opinion of the investigator or medical monitor.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02003924) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search