Aspirin as Adjuvant Therapy in Patients With Surgically Treated High Risk Renal Cell Carcinoma Clinical Trial
Official title:
Preventive Effects of Low-dose Aspirin as Adjuvant Therapy After Radical Nephrectomy on Disease Recurrence/Metastasis and Survival in Patients With Locally Advanced Renal Cell Carcinoma: an Observational Prospective Cohort Study
The study evaluates the protective effect of low-dose aspirin use as adjuvant therapy on locally advanced renal cell carcinoma in users and non-users of aspirin in Renji Hospital, Shanghai, China.
Status | Recruiting |
Enrollment | 260 |
Est. completion date | October 2024 |
Est. primary completion date | October 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients must complete radical surgery more than 4 weeks and less than 12 weeks prior to study entry - Patients must have histologically or cytologically confirmed renal cell carcinoma. Using 2017 (American Joint Committee on Cancer [AJCC] 8th edition) TNM Staging, patients must be one of the following: - pT2aG3 or G4N0M0 - pT2bG(any)N0M0 - pT3G(any)N0M0 - pT4G(any)N0M0 - pT(any)G(any)N1M0 - Patients must have no clinical or imaging evidence of visible residual lesions or distant metastases (M0) after nephrectomy - Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 - Patients must be able to swallow pills Exclusion Criteria: - Patients with haemorrhagic diathesis (i.e. haemophilia). - Patients with prior malignant tumors except for kidney cancers in the past 5 years. - Patients with documented or suspected metastases. - Patients with serious, nonhealing wound, ulcer, or bone fracture. - Patients with a history of stroke, coronary arterial disease, angina, or vascular disease. - Patients who are pregnant, lactating, or not using adequate contraception. - Patients who have known allergy to NSAID or Aspirin. - Patients receiving other antiplatelet agents (i.e. clopidogrel, ticlopidine) or anticoagulants (i.e. warfarin, low molecular weight heparins). - Patients receiving current long term treatment (=1 month) with Aspirin or other NSAIDs. - Subject unwilling or unable to comply with study requirements. |
Country | Name | City | State |
---|---|---|---|
China | Renji Hospital, School of Medicine, Shanghai Jiao Tong University | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
RenJi Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Disease-free Survival | Disease-free Survival | 36 mouths | |
Secondary | Overall survival | Overall survival | 36 months | |
Secondary | Cancer specific survival | Cancer specific survival | 36 months | |
Secondary | adverse event rate | Rate of patients with each of the adverse event per grade | 12 months |