Abstract. The aim of this study (JGOG1063) was to determine the recommended dose (RD) for combination chemotherapy with irinotecan hydrochloride (CPT-11) and nedaplatin (NDP) for advanced cervical squamous cell carcinoma. CPT-11 was given intravenously in fixed doses of 60 mg/m 2 on days 1 and 8 and NDP, in escalating doses, on day 1, every 4 weeks. A total of 15 patients were enrolled in the study. At level 1 (NDP: 50 mg/m 2 ), one of the 3 patients developed grade 3 diarrhea, so 3 additional patients were enrolled at this level. As none of the 3 additional patients exhibited dose-limiting toxicity, level 1 was elevated to level 2 (NDP: 60 mg/m 2 ). The maximum tolerated dose was not reached, even at the highest dose level (level 4; NDP: 80 mg/m 2 ). No further dose escalation was carried out, and level 4 (CPT-11: 60 mg/m 2 , NDP: 80 mg/m 2 ) was determined as the RD.