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Chemotherapy After Prostatectomy (CAP) For High Risk Prostate Carcinoma

CSP #553 - Adjuvant Therapy in Prostate Carcinoma Treatment

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00132301
Acronym
CAP
Enrollment
298
Registered
2005-08-19
Start date
2006-06-30
Completion date
2016-09-30
Last updated
2018-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

multi-site clinical trial, prostate, radical prostatectomy, randomized

Brief summary

VA Cooperative Study #553 is designed to prospectively evaluate the efficacy of early adjuvant chemotherapy using docetaxel and prednisone added to the standard of care for patients who are potentially cured by radical prostatectomy but who are at high risk for relapse. The standard of care is surveillance, with the addition of androgen deprivation at the time of biochemical relapse. This study will assess the effect of adding early chemotherapy to the standard of care on progression free survival in Veterans at high risk for progression after prostatectomy.

Detailed description

VA Cooperative Study #553 is designed to prospectively evaluate the efficacy of early adjuvant chemotherapy using docetaxel and prednisone added to the standard of care for patients who are potentially cured by radical prostatectomy but who are at high risk for relapse. The standard of care is surveillance, with the addition of androgen deprivation at the time of biochemical relapse. This study will assess the effect of adding early chemotherapy to the standard of care on progression free survival in Veterans at high risk for progression after prostatectomy. The ability of radical prostatectomy to cure prostate cancer and to therefore prevent the morbidity and mortality associated with progression to metastatic disease depends on effectively treating both local and potential systemic disease. In the United States alone, over 80,000 men per year are treated with prostatectomy to cure their disease. Because 20% of these men will be found to have locally advanced or high-grade disease, they will be at risk for relapse and morbidity from their prostate cancer. Although androgen deprivation, radiation therapy, and chemotherapy have been considered potentially effective adjuvant modalities for localized prostate cancer, there are no randomized studies that support the utility of any of these treatments as a standard of care. Ultimately, it is androgen independent prostate cancer, which causes morbidity for these patients. Docetaxel based chemotherapy has been shown to prolong survival and induce responses in up to 80% of patients with androgen independent disease, generating enthusiasm for the use of chemotherapy early in the treatment of prostate cancer. This study is designed to test the value of adjuvant chemotherapy in improving progression free survival, which is critical in preventing morbidity and mortality from relapse in patients with clinically localized, but high risk, prostate cancer. After patients are stratified for PSA, Gleason score, tumor stage, the presence of positive margins, and the planned use of adjuvant radiation therapy, this study will randomized 300 patients from 30 VA sites, after prostatectomy, to the standard of care or to docetaxel and prednisone administered every 3 weeks for 18 weeks. Patients would then be observed with PSA for a minimum of one and a maximum of five years. The study is designed with 90% power to detect a reduction in the 5-year progression rate from 60% to 45% (15% absolute difference, 25% relative difference). At the end of the study period (October 31, 2012), the patients in the study will continue to be passively followed for three more years. The follow-up study involved centralized remote access of the participants' medical records to obtain information on PSA levels and study endpoints. Prostate cancer is the leading cause of malignancy for Veterans, and the second leading cause of death. Patients with high risk, localized disease account for 70% of all cancer deaths in patients treated for cure with radical prostatectomy. Effective adjuvant therapy is critical to reducing suffering and death from prostate cancer. The VA Cooperative Studies Program is uniquely placed to address this question. The VA has a longstanding history of important studies in prostate cancer, which have significantly changed the way urologic oncologists treat patients with this disease. The incidence of prostate cancer in our older, male population is substantial, the number of Veterans treated with prostatectomy continues to rise, and the incidence of high risk prostate cancer in Veterans is greater than that typically found in the community. For all of these reasons, carrying out this study within the VA through the VA Cooperative Studies Program is the optimal way to determine whether adjuvant chemotherapy will benefit men with high risk prostate cancer.

Interventions

DRUGDocetaxel

Chemotherapy agent

DRUGPrednisone

steroid in combination with chemotherapy agent

Sponsors

Sanofi
CollaboratorINDUSTRY
VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The Endpoint Committee will adjudicate evidence for progression, metastasis, and cause of death. The committee will be blinded to the treatment assignment.

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* A histologic diagnosis of cT1-T2 primary adenocarcinoma of the prostate prior to prostatectomy, with lymph node dissection at time of radical prostatectomy * One or more of the following poor prognostic features: * tumor extension to seminal vesicle (pT3b) or bladder neck (T4) * established extracapsular extension (pT3a) and Gleason Score \>= 7 * organ confined (pT2) with positive surgical margin and Gleason 8-10 * preoperative PSA \> 20 * SWOG performance status 0-1 * PSA nadir of \<= 0.1 ng/ml up to 30 days prior to randomization. Patients must be randomized within 120 days after prostatectomy. * Laboratory values (no more than 30 days before randomization) must be as follows: * Absolute granulocyte count: \>= 1,500/mm3 * Platelets: \>= 100,000/mm3 * Hemoglobin: \>= 10 g/dL * Serum Creatinine: \<= 1.5 x ULN * AST: \<= 1.5 x ULN * ALT: \<= 1.5 x ULN * Serum Calcium: \<= ULN * Total Bilirubin: \<=ULN * Plasma Phosphorus Level: \<= 6 mg/dl * Patients with preoperative PSA \> 20 ng/mL must have a negative bone scan within 120 days of randomization * A valid, signed, and witnessed informed consent by the patient

Exclusion criteria

* Small cell histology * N1 disease or M1 disease * Clinical T3 disease prior to prostatectomy * Any other investigational therapy * An active serious infection or other serious underlying medical condition that would otherwise impair their ability to receive protocol treatment * A history of cancer related hypercalcemia * Uncontrolled heart failure * Prior malignancy other than curatively treated squamous cell or basal cell carcinoma of the skin. If another malignancy has been treated and there is no evidence of relapse \> 5 years from the time of treatment, patients are eligible * Androgen deprivation, chemotherapy, or radiation therapy to treat prostate carcinoma * Current peripheral neuropathy of any etiology that is greater than Grade I

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants With Progression-Free SurvivalUp to 100 months (centralized follow-up)The primary objective of this study is to determine whether adding early chemotherapy based on docetaxel plus prednisone compared to standard of care alone reduces disease progression as evidenced by detectable PSA in high risk patients with prostate cancer who have undergone radical prostatectomy.

Countries

Puerto Rico, United States

Participant flow

Participants by arm

ArmCount
Arm 1: Chemotherapy Agent and Prednisone
Chemotherapy after radical prostatectomy Docetaxel: Chemotherapy agent Prednisone: steroid in combination with chemotherapy agent
140
Arm 2: Standard of Care
Treatment by Standard of care
157
Total297

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyDeath76
Overall StudyExcluded by Data Monitoring Committee10
Overall StudyLost to Follow-up53
Overall StudyOther11
Overall StudyPhysician Decision11
Overall StudyWithdrawal by Subject52

Baseline characteristics

CharacteristicTotalArm 2: Standard of CareArm 1: Chemotherapy Agent and Prednisone
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
76 Participants42 Participants34 Participants
Age, Categorical
Between 18 and 65 years
221 Participants115 Participants106 Participants
Age, Continuous62.27 years
STANDARD_DEVIATION 5.6
63.0 years
STANDARD_DEVIATION 5.3
62.0 years
STANDARD_DEVIATION 6
Biopsy Gleason Score
<= 7
201 Participants104 Participants97 Participants
Biopsy Gleason Score
8 to 10
96 Participants53 Participants43 Participants
BMI
BMI < 25
57 Participants28 Participants29 Participants
BMI
BMI 25 to < 30
131 Participants71 Participants60 Participants
BMI
BMI >= 30
109 Participants58 Participants51 Participants
Clinical Stage
cT1
154 Participants87 Participants67 Participants
Clinical Stage
cT2a
64 Participants28 Participants36 Participants
Clinical Stage
cT2b
49 Participants24 Participants25 Participants
Clinical Stage
cT2c
29 Participants17 Participants12 Participants
Clinical Stage
unknown or not reported
1 Participants1 Participants0 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
28 Participants11 Participants17 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
269 Participants146 Participants123 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Pathology Stage
T2a, T2b, T2c
26 Participants15 Participants11 Participants
Pathology Stage
T3a
168 Participants87 Participants81 Participants
Pathology Stage
> T3b
103 Participants55 Participants48 Participants
Pre Biopsy PSA (ng/ml)
< 10
201 Participants110 Participants91 Participants
Pre Biopsy PSA (ng/ml)
10 to < 20
61 Participants30 Participants31 Participants
Pre Biopsy PSA (ng/ml)
>= 20
33 Participants16 Participants17 Participants
Pre Biopsy PSA (ng/ml)
Unknown or not reported
2 Participants1 Participants1 Participants
Pre Prostatectomy PSA (ng/ml)
< 10
191 Participants106 Participants85 Participants
Pre Prostatectomy PSA (ng/ml)
10 to < 20
70 Participants32 Participants38 Participants
Pre Prostatectomy PSA (ng/ml)
>=20
36 Participants19 Participants17 Participants
Prostatectomy Gleason Score
<= 7
11 Participants4 Participants7 Participants
Prostatectomy Gleason Score
7: 3+4
112 Participants60 Participants52 Participants
Prostatectomy Gleason Score
7: 4+3
71 Participants36 Participants35 Participants
Prostatectomy Gleason Score
8-10
103 Participants57 Participants46 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
74 Participants35 Participants39 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
16 Participants9 Participants7 Participants
Race (NIH/OMB)
White
207 Participants113 Participants94 Participants
Region of Enrollment
United States
297 Participants157 Participants140 Participants
Sex: Female, Male
Female
0 Participants0 Participants0 Participants
Sex: Female, Male
Male
297 Participants157 Participants140 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
79 / 1403 / 157
serious
Total, serious adverse events
47 / 14050 / 157

Outcome results

Primary

Number of Participants With Progression-Free Survival

The primary objective of this study is to determine whether adding early chemotherapy based on docetaxel plus prednisone compared to standard of care alone reduces disease progression as evidenced by detectable PSA in high risk patients with prostate cancer who have undergone radical prostatectomy.

Time frame: Up to 100 months (centralized follow-up)

Population: One participant in Arm 1 was excluded from analysis by the Data Monitoring Committee (DMC), making the analysis population in Arm 1 140 participants.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Arm 1: Docetaxel and PrednisoneNumber of Participants With Progression-Free Survival66 Participants
Arm 2: Standard of CareNumber of Participants With Progression-Free Survival84 Participants
p-value: 0.495% CI: [0.58, 1.11]Log Rank

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026