N/A
Completed N=18
Consensus Method to Evaluate the Conformity of Prescription of a Chemotherapy
Source: ClinicalTrials.gov NCT02882178 ↗Enrolled (actual)
18
Serious AEs
—
Results posted
Jan 2021
Primary outcomePrimary: Items to Define Conformity to Cabazitaxel Conditions of Use — 11 items
Summary
Cabazitaxel is a second line chemotherapy drug recently approved for the treatment of metastatic castration-resistant prostate cancer. To investigate whether the precautions for the use of cabazitaxel (contraindications, hepatic function, premedication for hypersensitivity, prophylactic treatments, dose and dose adjustment, as well as conditions of administration) are respected in routine practice, an observational cohort study will be implemented in 32 oncology centres of South-West region of France (CABOBS study). The primary objective of this cohort is to evaluate the conformity of cabazitaxel prescriptions with the Summary of Product haracteristics (SPC) in clinical practice (indications and monitoring methods) and according to the conditions of use. Panel of experts were convened to assess the conformity of prescription of cabazitaxel with a Delphi consensus method. The Delphi method is most suited to areas where a limited number of evidences are available to enable a recommendation or guidelines to be drawn. Moreover, all the evaluated items came from an official document provided by the EMA, the SPC of cabazitaxel. Thus, it is expected from the experts to select the most relevant items. In the frame of the CABOBS study, this method will allow to select items of the SPC list according to their importance, and to define the primary objective of conformity to cabazitaxel conditions of use.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Items to Define Conformity to Cabazitaxel Conditions of Use |
11 | — |
Eligibility Criteria
Eligibility criteria for the experts involved in the consensus process:
- experts in uro-oncology solicited within the French GETUG's group (Groupe d'Etude des Tumeurs Uro-Génitales)
- experts in uro-oncology solicited within the EORTC GU group for the second panel of experts.
Data sourced from ClinicalTrials.gov (NCT02882178). 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.