Background: Kidney cancer (KC) is associated with cardiovascular regulation disorder, which easily leads to cardiovascular and cerebrovascular death (CCD), and CCD is one of the major causes of death in patients with KC, especially in T1/2 status. However, there are few studies treated CCD as an independent outcome and analyzed the risk factors related to this outcome. We aimed to evaluate the key factors associated with CCD or kidney cancer-specific death (KCD) in patients with T1/2 KC by competing risk analysis, and compared these two kinds of risk factors to offer some information for clinical management. Methods: A total of 45117 patients diagnosed with first primary KC in T1/2 status between 2004-2015 were obtained from the Surveillance, Epidemiology, and End Results (SEER) database. According to their outcomes at the end of follow-up, all patients were divided into CCD group (n=3087), KCD group (n=3212), Other Events group (n=6312) and Alive group (n=32506). Patients’ clinical characteristics were estimated their association with CCD and KCD by Fine-Gray’s competing risk model. Factors significantly correlating with CCD or KCD were used to create forest plots to compare their differences.Results: The Fine-Gray’s competing risk analysis showed that age at diagnosis, race, marital status, tumor size, AJCC T stage, chemotherapy, kind of surgery of primary site and scope of lymph node were correlated significantly with CCD. Moreover, age at diagnosis, sex, marital status, tumor size, AJCC T/N status, radiation therapy, chemotherapy, kind of surgery of primary site and scope of lymph node were correlated significantly with KCD. Then the forest plots of these two kinds factors were established to compare their difference. It was found that age at diagnose, race, AJCC T/N status and therapy methods represented significantly different risks for patients with T1/2 KC developing to CCD or KCD.Conclusion: We firstly separated CCD and KCD as two independent outcomes to analysis the risk factors related them, and found that age at diagnose, race, AJCC T/N status and therapy methods differently affected patients with T1/2 KC developing to CCD or KCD.