The primary objective of this study was to determine the response rates of the gemcitabine and cisplatin combination in unresectable gall bladder cancer patients. The secondary objectives were to evaluate the toxicity, time to progressive disease, and overall survival. Chemonaïve patients with histologically proven, unresectable bidimensionally measurable gall bladder cancer were enrolled into this study. All patients were required to have a Zubrod's performance status

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409709PMC
http://dx.doi.org/10.1038/sj.bjc.6601736DOI Listing

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