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  4. Phase II study of biweekly gemcitabine followed by oxaliplatin and simplified 48-h infusion of 5-fluorouracil/leucovorin (GOFL) in advanced pancreatic cancer
 
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Phase II study of biweekly gemcitabine followed by oxaliplatin and simplified 48-h infusion of 5-fluorouracil/leucovorin (GOFL) in advanced pancreatic cancer

Journal
Cancer Chemotherapy and Pharmacology
Journal Volume
64
Journal Issue
6
Pages
1173-1179
Date Issued
2009
Author(s)
Ch'ang H.-J.
Huang C.-L.
HSIU-PO WANG  
Shiah H.-S.
MING-CHU CHANG  
Jan C.-M.
Chen J.-S.
YU-WEN TIEN  
Hwang T.-L.
Lin J.-T.
ANN-LII CHENG  
Whang-Peng J.
Chen L.-T.
DOI
10.1007/s00280-009-0980-2
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-69049099928&doi=10.1007%2fs00280-009-0980-2&partnerID=40&md5=96013a846cf027043958a3b24ce9809d
https://scholars.lib.ntu.edu.tw/handle/123456789/461876
Abstract
Purpose: To evaluate the efficacy and safety profile of a triplet regimen consisting of gemcitabine, oxaliplatin, and infusional fluorouracil and leucovorin (LV) in advanced pancreatic carcinoma (APC). Patients and methods: Chemotherapy-na?ve patients with histo-/cytologically proven unresectable APC, and bi-dimensionally measurable diseases were eligible. Treatment consisted of fixed-dose rate (10 mg/m2/min) infusion of 800 mg/m2 gemcitabine followed by 2-h infusion of 85 mg/m2 oxaliplatin and then 48-h infusion of fluorouracil and LV (3,000 and 300 mg/m2, respectively) every 2 weeks (the GOFL regimen). The primary end-point was objective response rate. Results: Forty-five patients were enrolled and received a median of seven [95% confidence interval (CI) 6.4-8.8] cycles of treatment. On intent-to-treat analysis, the overall response and disease-control rates were 33.3% (95% CI 21.4-48.0%) and 68.9% (95% CI 54.8-83.0%), respectively. Clinical benefit response was observed in 46.2% of initially symptomatic patients. The median time-to-tumor progression and overall survival were 5.1 (95% CI 4.0-6.3) months and 8.7 (95% CI, 6.1-11.3) months, respectively. Major grade 3-4 toxicities were neutropenia (28.9%, with 4.4% complicated with fever), peripheral sensory neuropathy (15.6%), nausea/vomiting (13.3%), and diarrhea (6.7%). Conclusions: The triplet regimen is feasible and exhibits promising activity against APC, deserving further exploration. ? 2009 Springer-Verlag.
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; fluorouracil; folinic acid; gemcitabine; oxalip; oxaliplatin; unclassified drug; adult; advanced cancer; aged; alanine aminotransferase blood level; anemia; article; asthenia; cancer combination chemotherapy; cancer patient; clinical article; clinical trial; diarrhea; drug efficacy; drug hypersensitivity; drug infusion; drug safety; drug withdrawal; feasibility study; febrile neutropenia; female; gastrointestinal hemorrhage; human; hyperammonemic encephalopathy; lung embolism; male; mucosa inflammation; multiple cycle treatment; nausea; neutropenia; overall survival; pancreas carcinoma; peripheral neuropathy; phase 2 clinical trial; priority journal; rash; sensory neuropathy; side effect; symptomatology; thrombocytopenia; treatment response; tumor growth; vomiting; Adult; Aged; Antineoplastic Agents; Deoxycytidine; Drug Administration Schedule; Drug Therapy, Combination; Female; Fluorouracil; Humans; Kaplan-Meiers Estimate; Leucovorin; Male; Middle Aged; Neoplasm Metastasis; Organoplatinum Compounds; Pancreatic Neoplasms; Survival Rate; Treatment Outcome
Type
journal article

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