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Japanese Journal of Clinical Oncology 2004 34(11):681-685; doi:10.1093/jjco/hyh124
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© 2004 Foundation for Promotion of Cancer Research

A Phase II Study of Paclitaxel plus Cisplatin Chemotherapy in an Unfavourable Group of Patients with Cancer of Unknown Primary Site

Yeon Hee Park, Baek-Yeol Ryoo, Seong-Jun Choi, Sung Hyun Yang and Heung-Tae Kim

Department of Internal Medicine, Korea Institute of Radiological and Medical Sciences, Seoul, Korea

For reprints and all correspondence: Yeon Hee Park, Division of Medical Oncology, Korea Cancer Center Hospital, 215-4, Gongneung-Dong, Nowon-ku, Seoul 139-706, Korea. E-mail: yhpark{at}kcch.re.kr

Received June 24, 2004; accepted September 23, 2004

Objective: We evaluated the efficacy and toxicity of combined paclitaxel and cisplatin chemotherapy in patients with cancer of unknown primary site (CUP). Efficacy was evaluated in terms of response rate, progression-free survival and overall survival.

Methods: Thirty-seven patients with CUP were enrolled between January 2001 and September 2003 at Korea Cancer Center Hospital. The patients received 21-day cycles of paclitaxel (175 mg/m2 i.v.) with cisplatin (60 mg/m2 i.v.) given on the first day.

Results: Of the 37 patients, 31 had adenocarcinoma subtypes. The overall response rate of 26 patients with measurable lesions was 42% [95% confidence interval (CI) 23–61%]. Stable disease was seen in six patients and progressive disease in nine. Median time to progression was 4 months (95% CI 1.3–6.8). Median overall survival was 11 months (95% CI 8.3–13.5). The major toxicities were neuropathy and neutropenia. Grade 4 neutropenia occurred in 10 patients, but febrile neutropenia was seen in four.

Conclusions: This combined paclitaxel and cisplatin regimen was well tolerated with an encouraging level of effectiveness for patients with CUP.

Key Words: carcinoma of unknown primary site (CUP) • cisplatin • paclitaxel


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