Clinical trial · Interventional
Follow-up After Metastasectomy in Patients With Kidney Cancer
A Phase II Metastasectomy Study for Patients With Renal Cell Carcinoma
NCT00918775CI-TRIAL-00108270active not recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This phase II trial studies the follow-up after metastasectomy in patients with kidney cancer. Following up patients' health condition after metastasectomy may help doctors to learn if the surgical removal of the primary tumor or the parts of the cancer that has spread to other parts of the body is a good method for treating patients who have kidney cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Renal Cell Carcinoma | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Follow-Up Care | Other | — | UNRESOLVED |
| Laboratory Biomarker Analysis | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Observational (follow-up)
- description
- After metastasectomy, patients are followed up every 6 months for up to 5 years.
- interventionNames
- Other: Follow-Up Care
- Other: Laboratory Biomarker Analysis
Primary outcomes (1)
- measure
- Binary indicator that the patient is alive with no evidence of disease progression (either progression or relapse) post surgery
- timeFrame
- 24 weeks
- description
- Assessed using a logistic regression model.
Secondary outcomes (3)
- measure
- Progression free survival (PFS)
- timeFrame
- Up to 5 years
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * Patients with histologically or cytologically confirmed renal cell carcinoma (RCC) * Patients have clinical reasons for undergoing a surgical resection of tumor; there are two main categories of patients: * Patients with fully resectable disease as defined by lesions accessible by a surgeon during no more than two separate surgical sessions, and are expected to be rendered surgically no evidence of disease (NED) * Patients undergoing a noncurative procedure for relief of symptoms or for management of threatening lesions * Patients have been deemed resectable by the subspecialty surgeon involved in the patient's care * Patients must give written informed consent prior to initiation of therapy, in keeping with the policies of the institution; patients with a history of major psychiatric illness must be judged able to fully understand the investigational nature of the study and the risks associated with the therapy; the only approved consent is attached to this protocol * Patients must have ability to comply with study and/or follow-up procedures * Members of all races and ethnic groups are eligible for this trial Exclusion Criteria: * Patients must not have active acute infections that could be worsened by surgery or interfere with this study * Patients must not have clinically significant cardiovascular disease, or peripheral vascular disease that creates an unacceptably high operative risk * Patients must not have history of other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates surgical resection, or render the subject at high risk from treatment complications * Patients must not have a history of uncontrolled severe depression
References
Publications (0)
Data not yet available
No reference posted for this study.