Combination of Cabazitaxel With Prednisolone With Primary Prophylaxis With PEG-G-CSF in Treatment of Patients With Prostate Cancer
Summary
Primary Objective: To assess the tolerability of cabazitaxel 25 mg per body surface area (m\^2) with primary prophylactic polyethylene glycol-granulocyte-colony stimulating factor (PEG-G-CSF) in terms of the incidence rate of febrile neutropenia (FN) (defined: absolute neutrophil count \[ANC\] \<1000 per volume \[mm\^3\] and a single temperature of \>38.3 degree or a sustained temperature of ≥38 degree Celsius for more than one hour) during Cycle 1. Secondary Objective: To assess overall rate of FN and grade ≥3 neutropenia and diarrhea; frequencies of dose delay due to adverse events (AEs); dose reduction due to AEs; relative dose intensity; incidences of FN-related hospitalization and use of intravenous (IV) anti-infectives; tolerability according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v4.0; prostate specific antigen (PSA) response (50% decrease); tumor response according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 if available.
Timeline
- Start
- 2015-04
- Primary completion
- 2016-02
- Completion
- 2016-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cabazitaxel | Other / unclassified | 25 mg/m2 | Intravenous |
| Subject | Pegfilgrastim | Protein / enzyme biologic | 3.6 mg | Subcutaneous |
| Background | Dexamethasone | Small molecule | — | Oral |
| Background | Dexchlorpheniramine | Unknown | — | Oral |
| Background | Diphenhydramine | Unknown | — | Oral |
| Background | Granisetron | Other / unclassified | — | Oral |
| Background | Metoclopramide | Small molecule | — | Oral |
| Background | Ondansetron | Other / unclassified | — | Oral |
| Background | Prednisolone | Other / unclassified | 10 mg | Oral |
| Background | Ranitidine | Unknown | — | Oral |