Interleukin-2/interferon- α 2a/13-retinoic acid-based chemoimmunotherapy in advanced renal cell carcinoma: results of a prospectively randomised trial of the German Cooperative Renal Carcinoma Chemoimmunotherapy Group (DGCIN)

We performed a prospectively randomised clinical trial to compare the efficacy of four subcutaneous interleukin-2-(sc-IL-2) and sc interferon- α 2a (sc-IFN- α 2a)-based outpatient regimens in 379 patients with progressive metastatic renal cell carcinoma. Patients with lung metastases, an erythrocyte sedimentation rate ⩽70 mm h −1 and neutrophil counts ⩽6000 μ l −1 (group I) were randomised to arm A: sc-IL-2, sc-IFN- α 2a, peroral 13- cis -retinoic acid (po-13cRA) ( n =78), or arm B: arm A plus inhaled-IL-2 ( n =65). All others (group II) were randomised to arm C: arm A plus intravenous 5-fluorouracil (iv-5-FU) ( n =116), or arm D: arm A plus po-Capecitabine ( n =120). Median overall survival (OS) was 22 months (arm A; 3-year OS: 29.7%) and 18 months (arm B; 3-year OS: 29.2%) in group I, and 18 months (arm C; 3-year OS: 25.7%) and 16 months (arm D; 3-year OS: 32.6%) in group II. There were no statistically significant differences in OS, progression-free survival, and objective response between arms A and B, and between arms C and D, respectively. Given the known therapeutic efficacy of sc-IL-2/sc-INF- α 2a/po-13cRA-based outpatient chemoimmunotherapies, our results did not establish survival advantages in favour of po-Capecitabine vs iv-5-FU, and in favour of short-term inhaled-IL-2 in patients with advanced renal cell carcinoma receiving systemic cytokines.