Renal Cell Carcinoma
Conditions
Keywords
Renal Cell Carcinoma (clear cell or non-clear cell)
Brief summary
The purpose of the protocol is to assess the Overall Survival (OS) at 1 year in patients after cabozantinib initiation.
Interventions
None listed
Sponsors
Ipsen
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Male or female ≥ 18 age at the time of cabozantinib initiation * Pathologically confirmed diagnosis of Renal Cell Carcinoma (Clear Cell or non-Clear Cell) cancer considered as advanced or metastatic at the time of cabozantinib initiation * Intention to be treated with cabozantinib tablets according to the current local Summary of Product Characteristics (SmPC) (France) * Initiating cabozantinib as a second line of treatment (Baseline visit must be performed before cabozantinib first intake)
Exclusion criteria
* He/she is already included in an interventional trial with an investigational product at the same time.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival (OS) rate at 1 year after cabozantinib initiation | up to 12 months | OS is the time between treatment initiation and the date of death from any cause. For participants who are alive, their survival time will be censored at the last date that they were known to be alive if before 1 year. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Objective Response Rate (ORR) at 1 year | Day 15, 1 month, 3, 6 and 12 months | ORR is defined as the proportion of participants who achieve partial or complete response from the start of the study treatment. The ORR will be assessed by tumour response evaluation according to investigator assessment. Tumour response will be evaluated per routine clinical practice by the physician. |
| Best Overall Response (BOR) at 1 year | Day 15, 1 month, 3, 6 and 12 months | BOR is the best response recorded from the start of the study treatment until the disease progression/recurrence. The BOR will be assessed by tumour response evaluation according to investigator assessment. Tumour response will be evaluated per routine clinical practice by the physician. |
| Progression Free Survival (PFS) at 1 year | Day 15, 1 month, 3, 6 and 12 months | PFS is defined as the time elapsed from the date of first treatment intake to the date of documented progression reported by the investigator or death due to any cause, whichever occurs first. Disease progression will be assessed by tumour response evaluation according to investigator assessment. Tumour response will be evaluated per routine clinical practice as Progressive / not progressive disease by the physician. |
| Previous systemic neoadjuvant and adjuvant therapies for RCC prior cabozantinib initiation in terms of nature of the therapy, duration, and reason for discontinuation. | Baseline | — |
| Pattern of use of cabozantinib | Baseline, day 15, 1 month, 3, 6 and 12 months | Dose modification, reason of modification and treatment duration of cabozantinib will be described from cabozantinib initiation until participants' end of study treatment or study withdrawal. |
| Quality of life (QoL) change according to Functional Assessment of Cancer Therapy (FKSI-19) questionnaire | Baseline, day 15, 1 month, 3, 6 and 12 months | QoL change from baseline. The score will be evaluated with FKSI 19 questionnaires at the planned visits and at treatment discontinuation. The FKSI-19 is a disease-specific instrument that measures disease and treatment-related symptoms in 4 domains by using a 5-point scale (0=not at all, 1=a little bit, 2=somewhat, 3=quite a bit, 4=very much). Higher scores represent better health. A negative change from Baseline represents a worsening of condition. |
| Pain assessment | Baseline, day 15, 1 month, 3, 6 and 12 months | To assess pain according to the Brief Pain Inventory-Short Form (BPI-SF) questionnaire and analgesic consumption/duration and the time for improvement of symptomatology. BPI-SF has a scale of 0 to 10 with 0 indicating No pain and 10 indicating Pain as bad as you can imagine. |
| Subsequent systemic treatment for RCC after cabozantinib discontinuation in terms of the description of the nature of the therapy, starting date. | End of Study visit (12 months if the patient didn't discontinue earlier) | — |
| Safety of cabozantinib in the real-world setting | Day 15, 1 month, 3, 6 and 12 months | Incidence of Adverse Events (AEs),Serious Adverse Events (SAEs) assessed overall and by intensity and causality. |
| First-line therapy for RCC prior cabozantinib initiation in terms of nature of the therapy, duration, and reason for discontinuation. | Baseline | — |
Outcome results
None listed