Phase 3
Completed N=1,401
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.
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.
-
US Population Reference Values for Health-Related Quality of Life Questionnaires Based on Demographics of Patients with Prostate Cancer.
-
Radiographic Progression With and Without Prostate-Specific Antigen Rise in Patients With Advanced Prostate Cancer Treated With Enzalutamide.
-
From Androgen Deprivation to Precision Therapy: A Bibliometric Review of Global Research Trends (2008-2023).
-
Which traits affect how long patients with advanced prostate cancer live when treated with enzalutamide?
Outcome Measures
| Outcome | Result | p-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.
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.