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Gemcitabine and oxaliplatin combination as first-line treatment for advanced pancreatic cancer: a multicenter phase II study

Authors
Lee, Kyung HeeKim, Min KyoungKim, Yeol HongRyoo, Baek YeolLim, Ho YeongSong, Hong SukKim, Hoon KyoLee, Myung AhIm, Seock AhChang, Heung MoonCho, Jae YongZang, Dae YoungKim, Bong SeogKim, Jun Suk
Issue Date
Jul-2009
Publisher
SPRINGER
Keywords
Advanced pancreatic cancer; Combination chemotherapy; Gemcitabine; GEMOX; Oxaliplatin
Citation
CANCER CHEMOTHERAPY AND PHARMACOLOGY, v.64, no.2, pp.317 - 325
Indexed
SCIE
SCOPUS
Journal Title
CANCER CHEMOTHERAPY AND PHARMACOLOGY
Volume
64
Number
2
Start Page
317
End Page
325
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/119711
DOI
10.1007/s00280-008-0873-9
ISSN
0344-5704
Abstract
Gemcitabine is the only drug approved for single-agent therapy in advanced pancreatic carcinoma (APC). Gemcitabine-based combination chemotherapy has not yet shown promising results. This multicenter phase II study enrolled previously untreated patients with locally advanced and/or metastatic pancreatic adenocarcinoma. Patients received 1,000 mg/m(2) gemcitabine, 100-min infusion, day 1 and 100 mg/m(2) oxaliplatin, 2-h infusion, day 2; q2w. The primary end point was response rate (RR). Thirteen study centers enrolled 48 eligible patients of which 44 were evaluable. The RR, median overall survival, and median time to progression were 18.2%, 9.4 and 5.6 months, respectively. Sixteen patients (36.4%) experienced clinical benefit. The global quality of life scores improved by 11.71. Grade 3/4 peripheral sensory neuropathy was noted (2.1%), while the most common hematologic toxicity was anemia (grade 3/4, 6.3%). Gemcitabine and oxaliplatin combination chemotherapy showed a promising activity in APC patients and was well tolerated.
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