EDITORIAL nale et Médicaments Anticancéreux-Renal Insufficiency and Anticancer Medications). These two cohorts included about 10,000 adult cancer patients with solid tumors (mainly breast, colorectal, and lung). Approximately half of them were nonmetastatic at the time of inclusion, and not on dialysis (1, 2). In these cohorts, 52.9% and 50.2% of the patients in IRMA-1 and IRMA-2, respectively, had a reduced eGFR (lower than 90 mL/min/1.73 m²), and 12.0% and 11.8% had stage 3 or 4 RI (lower than 60 mL/min/1.73 m²). Interestingly, cancer patients rarely present with a normal eGFR. Several other studies have reported on the prevalence of RI in cancer patients. For instance, in patients with kidney cancer, Huang et al (3) reported a particularly high (87%) prevalence of abnormal renal function (lower than 90 mL/min/1.73 m²) in a cohort of 662 patients with a renal cortical tumor (<4 cm) awaiting partial or radical nephrectomy. The prevalence of an eGFR lower than 60 mL/min/1.73 m² was also higher than the one reported in the IRMA studies, with 26% of the patients with at stage 3-4 RI. Other studies in Belgium (4), the USA (5), Japan (6), and Austria (7) reported the prevalence of an eGFR <60 mL/min/1.73 m 2 of 16.1%, 22.0%, 25.0%, and 14.7 to 16.1%, respectively. In the IRMA-2 study, the potential impact of RI on patient survival had been assessed through a 2-year follow-up. The results showed that patients with an eGFR lower than 60 mL/min/1.73 m² at the time of inclusion in the study had a significantly lower survival rate compared to patients with an eGFR greater than or equal to 60 mL/min/1.73 m². Considering the 2,382 patients who had a nonmetastatic disease, the impact of RI on survival was still significant. The survival was 21.0 vs. 25.0 months for patients with an eGFR lower than or equal to 60 mL/min/1.73 m², respectively.