Trial Evaluating the Safety of 2 Schedules of Cabazitaxel in Elderly Men With mCRPC Previously Treated With a Docetaxel

Association Pour La Recherche des Thérapeutiques Innovantes en Cancérologie196 enrolled

Overview

The purpose of this study is to evaluate the incidence of grade ≥ 3 neutropenia and/or neutropenic complications (febrile neutropenia, neutropenic infection) with two schedules of cabazitaxel (bi-weekly versus tri-weekly) plus prednisone in elderly men (≥ 65 years) with mCRPC previously treated with a docetaxel-containing regimen.

Randomized, open-label, phase 3 trial in mCRPC patients aged ≥ 65 years. Number of subjects: Total:170 to 200 (85 to 100 per arm) Treatment: * Arm A : cabazitaxel 25 mg/m² on Day 1 of a 3-week cycle plus daily prednisone or * Arm B: cabazitaxel 16 mg/m² on Day 1 and Day 15 of a 4-week cycle plus daily prednisone. * Treatment will be continued for a maximum of 10 cycles unless there is documented disease progression or unacceptable toxicity. * Standard cabazitaxel premedication will be used * Prophylactic G-CSF (GRANOCYTE) will be injected from Day 3 to Day 7 after every administration cycle of cabazitaxel· All new hormonal treatment, including ODM-201, prior to study entry is allowed. * Patients who received Radium-223 are eligible for this study * Treatment with LHRH should not be discontinued. Exploratory assessments: CT-Scan (abdominal/pelvic/chest) or whole body MRI and Bone scan: at screening, every 3 months and EOT. FACT-P questionnaire:at C1D1,each subsequent visit and EOT Exploratory substudy Blood samples will be collected in France (4 or 6 sites) and the Netherlands (2 sites). Biomarker analysis will be conducted at the Urology and The Tumor Immunology Laboratory at Radboud UMC in NL. Biomarker schedule Arm A (25mg/m2): Baseline - Week 6 - Week 12 - at progression Arm B (16mg/m2): Baseline - Week 6 - Week 12 - at progression Optional sample points are at C1D8. Number of subjects: 50 Statistical analysis: A sample size of 77 to 90 evaluable patients per arm will achieve 80% power to detect a 20% difference in G3 neutropenia incidence between the 2 arms. The incidence in group cabazitaxel 25 mg/m2 q3w is assumed to be 32% and 12% on bi-weekly cabazitaxel arm. The test used is a two-sided Fisher's exact test at 0.05 significance level. Assuming 10% non-evaluable patients, 85 to 100 patients should be included in each arm for a total of 170 to 200. Patients will be stratified according to G8 score (\< 14 vs. ≥ 14), and age (\< 70 vs. ≥ 70) before randomization. Exploratory sub-study The trial is powered on a clinical endpoint, namely to detect a 20% difference in G3 nThe trial is powered on a clinical endpoint, namely to detect a 20% difference in G3 neutropenia incidence between arms (32% in arm A vs 12% arm B; power 80% with two-sided alpha of 5%, correcting for 10% non-evaluable patients (=17 patients). From the 153 to 180 evaluable patients, we have 76 to 90 patients in each arm, of which we expect 40-60 evaluable patients for translational studies (calculations performed on 25 per arm). In arm A, we expect 8 patients (32% of patients) with G3 neutropenia, and 17 patients that do not. In arm B, we expect 3 patients (12% of patients) with G3 neutropenia, and 22 patients that do not. For the MDSC analyses, we therefore will be comparing 11 patients with G3 neutropenia to 39 patients. For all continuous variables, including all immune subpopulations present in blood, mean (sd) will be presented if the distribution seems to be symmetric and in case of a skewed distribution the median and IQR. For categorical data, number and percentage will be presented. For comparison of continuous data linear regression analyses or correlation (Spearman or Pearson) will used. For comparison of continuous data with categorical data logistic regression analysis will be used. For comparison of two sets of categorical data the chi-square test of Fisher's exact test will be utilized. For the radiological PFS analyses the estimates of the hazard ratio and corresponding 95% confidence interval will be tested using a Cox Proportional hazard model. For the overall survival, a stratified log-rank test will be used to compare between groups.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

196

Conditions

Prostate Cancer Metastatic

Interventions

cabazitaxelDRUG

* Arm A : cabazitaxel 25 mg/m² on Day 1 of a 3-week cycle plus daily prednisone or * Arm B: cabazitaxel 16 mg/m² on Day 1 and Day 15 of a 4-week cycle plus daily prednisone. * Treatment will be continued for a maximum of 10 cycles unless there is documented disease progression or unacceptable toxicity. * Standard cabazitaxel premedication will be used

PrednisoneDRUG

Arm A:plus prednisone 10 mg orally given daily for a maximum of 10 cycles Arm B: plus prednisone 10 mg orally given per day up to 10 cycles

Granulocyte colony-stimulating factor (G-CSF)DRUG

Primary prophylaxis with Granulocyte Colony-Stimulating Factor (G-CSF) will be injected from Day 3 to Day 7 after every administration of cabazitaxel

Eligibility

Sex: MALEMin age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patient aged ≥ 65 years with mCRPC previously treated with docetaxel 2. Medical or surgical castration with castrate level of testosterone (\< 50 ng/dl) based on the EAU definition of castrate level of testosterone 3. Progressive disease according to PCWG2 4. Histologically proven prostate carcinoma 5. Health status allowing use of chemotherapy: G8 \> 14; or G8 score ≤ 14 with geriatric assessment concluding to reversible impairment allowing use of chemotherapy 6. ECOG-PS 0, 1 or 2(ECOG-PS 2 should be related to prostate cancer) 7. Adequate hematologic, liver and renal functions: 1. Neutrophil count ≥1.5 109/L 2. Haemoglobin ≥10 g/ dL 3. Platelet count ≥100.109/L 4. Total bilirubin ≤ 1 the upper limit of normal (ULN) 5. Transaminases ≤ 1.5 ULN 6. Serum creatinine ≤ 2.0 ULN 8. Ongoing LHRH therapy at study entry 9. Signed informed consent Exclusion Criteria: 1. History of severe hypersensitivity reaction (≥grade 3) to docetaxel 2. History of severe hypersensitivity reaction (≥grade 3) to polysorbate 80 containing drugs 3. Uncontrolled severe illness or medical condition (including uncontrolled diabetes mellitus) 4. Concurrent or planned treatment with strong inhibitors or strong inducers of cytochrome P450 3A4/5 (a one week wash-out period is necessary for patients who are already on these treatments) (see Appendix E) 5. PS \>2 not related to prostate cancer disease 6. G8 ≤ 14 with geriatric assessment contra-indicating standard cabazitaxel regimen 7. Concomitant vaccination with yellow fever vaccine 8. Patient who cannot be regularly followed or cannot answer to quality of life questionnaires because of psychological, social, familial or geographic reasons 9. Participation in another clinical trial with any investigational drug within 30 days prior to study enrolment.

Locations (31)

Outcomes

Primary Outcomes

Number of grade ≥ 3 neutropenia and/or neutropenic complications

To evaluate the incidence of grade ≥ 3 neutropenia (measured at Day 7 and Day 14) and/or neutropenic complications (febrile neutropenia, neutropenic infection) with two schedules of cabazitaxel (bi-weekly versus tri-weekly) plus prednisone in elderly men (≥ 65 years) with mCRPC previously treated with a docetaxel-containing regimen. with two schedules of -+cabazitaxel (bi-weekly versus tri-weekly) plus prednisone in elderly men with mCRPC previously treated with a docetaxel-containing regimen

Time frame: Up to 11 months

Secondary Outcomes

Dose reductions

Up to 11 months

Time frame: through study completion, an average of 40 weeks

Radiological progression-free survival (rPFS)

CT-Scan (abdominal/pelvic/chest) or whole body MRI and Bone scan

Time frame: Up to 11 months

Time to PSA progression

Assessed at C1D1, at every each subsequent visit and EOT

Time frame: Up to 11 months

Time to first symptomatic Skeletal-Related Event (SRE) and incidence of SREs

Assessed at C1D1, at every each subsequent visit and EOT

Time frame: Up to 11 months

Time to opioid treatment (if relevant)

Time frame: Up to 11 months

Prostate-specific antigen (PSA) response rate

Assessed at C1D1, at every each subsequent visit and EOT

Time frame: Up to 11 months

Data from ClinicalTrials.gov

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