Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma

Objectives: The prognosis for patients with unresectable biliary tract cancer is poor and existing chemotherapy is relatively ineffective. Therefore, a need exists for new, effective chemotherapeutic regimens. The aim of this study was to determine the efficacy and safety profile of gemcitabine plus...

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Main Authors: S. Thongprasert, S. Napapan, C. Charoentum, S. Moonprakan
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/62115
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spelling th-cmuir.6653943832-621152018-09-11T09:27:06Z Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma S. Thongprasert S. Napapan C. Charoentum S. Moonprakan Biochemistry, Genetics and Molecular Biology Medicine Objectives: The prognosis for patients with unresectable biliary tract cancer is poor and existing chemotherapy is relatively ineffective. Therefore, a need exists for new, effective chemotherapeutic regimens. The aim of this study was to determine the efficacy and safety profile of gemcitabine plus cisplatin in patients with unresectable biliary tract cancer (cholangiocarcinoma) and gall bladder cancer. Methods: From December 2000 to July 2002, 43 patients received gemcitabine 1250mg/m 2 in a 30-min i.v. infusion on d1, 8 and cisplatin 75 mg/m 2 in a 2-h i.v. infusion on d1 (with appropriate hydration), every 3 weeks. Eligibility: Normal hematologic parameters and creatinine levels; serum bilirubin <5 mg/dl. Results: Forty-three patients enrolled; 40 were assessable (three patients were not assessable due to incomplete treatment; they chose to discontinue chemotherapy after the first cycle). There were 23 males and 17 females, median age 50 years (range 31-69), median Karnofsky PS 80%. Tumor types: cholangiocarcinoma (39), gall bladder cancer (1). Median number of chemotherapy courses was four (range 1-8). Overall response rate was 27.5% (PR in 11 pts), with 32.5% SD and/or minor response. Median survival time was 36 weeks. Grade 3 hematologic toxicity: anemia (4.33%), leukopenia (1.73%). Non-hematologic toxicity (i.e. rash, nausea, vomiting, neuropathy and myalgia) ranged from mild to moderate. Conclusions: Gemcitabine plus cisplatin is active in biliary tract carcinoma. These data warrant further investigation of single-agent gemcitabine versus gemcitabine plus cisplatin or its derivative, i.e. oxaliplatin. © 2005 European Society for Medical Oncology. 2018-09-11T09:22:05Z 2018-09-11T09:22:05Z 2005-02-01 Journal 09237534 2-s2.0-14644410398 10.1093/annonc/mdi046 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=14644410398&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62115
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
S. Thongprasert
S. Napapan
C. Charoentum
S. Moonprakan
Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
description Objectives: The prognosis for patients with unresectable biliary tract cancer is poor and existing chemotherapy is relatively ineffective. Therefore, a need exists for new, effective chemotherapeutic regimens. The aim of this study was to determine the efficacy and safety profile of gemcitabine plus cisplatin in patients with unresectable biliary tract cancer (cholangiocarcinoma) and gall bladder cancer. Methods: From December 2000 to July 2002, 43 patients received gemcitabine 1250mg/m 2 in a 30-min i.v. infusion on d1, 8 and cisplatin 75 mg/m 2 in a 2-h i.v. infusion on d1 (with appropriate hydration), every 3 weeks. Eligibility: Normal hematologic parameters and creatinine levels; serum bilirubin <5 mg/dl. Results: Forty-three patients enrolled; 40 were assessable (three patients were not assessable due to incomplete treatment; they chose to discontinue chemotherapy after the first cycle). There were 23 males and 17 females, median age 50 years (range 31-69), median Karnofsky PS 80%. Tumor types: cholangiocarcinoma (39), gall bladder cancer (1). Median number of chemotherapy courses was four (range 1-8). Overall response rate was 27.5% (PR in 11 pts), with 32.5% SD and/or minor response. Median survival time was 36 weeks. Grade 3 hematologic toxicity: anemia (4.33%), leukopenia (1.73%). Non-hematologic toxicity (i.e. rash, nausea, vomiting, neuropathy and myalgia) ranged from mild to moderate. Conclusions: Gemcitabine plus cisplatin is active in biliary tract carcinoma. These data warrant further investigation of single-agent gemcitabine versus gemcitabine plus cisplatin or its derivative, i.e. oxaliplatin. © 2005 European Society for Medical Oncology.
format Journal
author S. Thongprasert
S. Napapan
C. Charoentum
S. Moonprakan
author_facet S. Thongprasert
S. Napapan
C. Charoentum
S. Moonprakan
author_sort S. Thongprasert
title Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
title_short Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
title_full Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
title_fullStr Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
title_full_unstemmed Phase II study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
title_sort phase ii study of gemcitabine and cisplatin as first-line chemotherapy in inoperable biliary tract carcinoma
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=14644410398&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62115
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