TY - JOUR T1 - Salvage chemotherapy with a combination of paclitaxel, ifosfamide, and cisplatin for the patients with recurrent carcinoma of the uterine cervix JF - International Journal of Gynecologic Cancer JO - Int J Gynecol Cancer SP - 1157 LP - 1164 DO - 10.1136/ijgc-00009577-200605000-00032 VL - 16 IS - 3 AU - C. H. Choi AU - T.-J. Kim AU - S.-J. Lee AU - J.-W. Lee AU - B.-G. Kim AU - J.-H. Lee AU - D.-S. Bae Y1 - 2006/04/01 UR - http://ijgc.bmj.com/content/16/3/1157.abstract N2 - The aim of this study was to assess the efficacy and toxicities of a combination of paclitaxel, ifosfamide, and cisplatin (TIP) for recurrent carcinoma of the uterine cervix. Fifty-three patients with recurrent cervical carcinoma were treated with ifosfamide 1500 mg/m2 intravenously over 3 h on days 1–3, paclitaxel 135 mg/m2 as a 3-h intravenous infusion, and cisplatin 50 mg/m2 intravenously over 30 min on day 1. The chemotherapy was repeated every 3 weeks until there was disease progression or unacceptable toxicity. Forty-five patients received at least three courses of treatment and were evaluable for their response. Twenty-one patients (46.7%) showed objective responses, including 4.4% complete responses and 42.2% partial responses. The median time to progression and the overall survival for all the patients were 8.0 months (95% confidence interval [CI], 7.1–8.9 months) and 19.0 months (95% CI, 11.9–26.1 months), respectively. The median duration of response was 9.0 months. Patients who had previously been treated with another chemotherapy after tumor recurrence showed a moderate response rate (29.4%) but a shorter time to progression (6 vs 8 months, P = 0.0421) and a shorter survival (11 vs 39 months, P = 0.0018). Patients with good performance status showed a higher response rate (63.6% vs 30.4%, P = 0.026) and a longer time to progression (9 vs 7 months, P = 0.0049). Patients with recurrent disease only outside the previous radiotherapy (RT) field exhibited a slightly higher response without statistical significance (60.0% vs 36.0%, P = 0.109). Grade 3 or 4 toxicities included neutropenia in 13% of patients and neurotoxicity in 5%. Three deaths during treatment were observed, but two of them were due to disease progression. We conclude that the combination chemotherapy with TIP yields a high response rate with acceptable toxicity for patients with recurrent cervical carcinoma, including those patients who have failed to respond to prior platinum-based chemotherapy. ER -