N/A
N=62
REGISTRY OF COMPLETE RESPONSES TO SUNITINIB IN SPANISH PATIENTS WITH METASTATIC RENAL CELL CARCINOMA
Carcinoma, Renal Cell
Bottom Line
View on ClinicalTrials.gov: NCT03916458 ↗Enrolled (actual)
62
Serious AEs
14.5%
Results posted
Dec 2021
Primary outcome: Primary: Time to Complete Remission of Lesions — 10.9; 15.7 Months
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Pediatric, Adult, Older Adult · 0+ yrs
- Sex
- All
- Sponsor
- Pfizer
- Primary completion
- Nov 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Complete Remission of Lesions |
10.9; 15.7 | — |
| PRIMARY Duration of Complete Remission (DOR) |
64.1; 62.2 | — |
| PRIMARY Progression Free Survival (PFS) |
NA | — |
Summary
Observational, retrospective, multicentre study in spanish patients with metastatic Renal Cell Carcinoma (mRCC) treated with sunitinib as a first-line treatment (treatment with previous cytokine therapy is accepted) according to clinical practice who obtained a complete response (CR) to treatment in one of these 2 situations:
1. Complete response (CR) obtained exclusively with first-line sunitinib treatment (sunitinib CR).
2. Response obtained after a period of time on treatment with sunitinib in which local treatment was also performed (surgery of the residual metastasis/metastases, radiofrequency ablation or radiotherapy) to achieve the total macroscopic disappearance of the disease, according to the opinion of the physician responsible for the patient (CR + local treatment).
Eligibility Criteria
Inclusion Criteria
- Patients who are 18 year-old or over who have been treated for metastatic renal cell carcinoma with sunitinib as first-line treatment (treatment with prior cytokine therapy is accepted) between 2007 and 30 September 2018 and who have obtained as a best treatment response the total remission of the disease in the opinion of the doctor in charge from a clinical, radiological and/or macroscopic point of view. This response must have been reached through two possible strategies:
A) Systemic treatment with sunitinib alone. B) Treatment with sunitinib and subsequent local treatment for one or more residual lesions that have not responded to the drug (traditional surgery, radiotherapy, SBRT (Stereotactic Body Radiation Therapy)).
- The duration of CR must have been confirmed with at least 2 consecutive imaging tests, without having a limit in the duration of this response. Although the patient had progressed subsequently, he/she may be included in this registry.
- Patients from any risk group
- Tumours of any histology
Exclusion Criteria
- Patients treated with another drug other than Sunitinib.
- Patients with no radiology reports proving CR.
- Patients with no record of the dose and regimen received with Sunitinib.
- Patients who achieved complete remission after 30 September 2018.
Data sourced from ClinicalTrials.gov (NCT03916458). 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.