Phase I clinical study of three times a day oral administration of TAS-102 in patients with solid tumors.
Publication
, Journal Article
Overman, MJ; Kopetz, S; Varadhachary, G; Fukushima, M; Kuwata, K; Mita, A; Wolff, RA; Hoff, P; Xiong, H; Abbruzzese, JL
Published in: Cancer Invest
October 2008
TAS-102 is a novel formulation of the fluorinated pyrimidine analogue trifluorothymidine (FTD) with an inhibitor of thymidine phosphorylase. The purpose of this study was to determine the MTD and DLT for TAS-102 administered three times a day on days 1-5 and 8-12 every 4 weeks. Fifteen patients were enrolled with two patients experiencing dose-limiting fatigue and granulocytopenia at the first dose level (80 mg/m2/day). Granulocytopenia was the primary toxicity: 7 patients experienced grade 3 or 4 granulocytopenia with the first course. No responses were noted, but nine patients demonstrated prolonged stable disease in this heavily pretreated 5-FU refractory population.
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Published In
Cancer Invest
DOI
EISSN
1532-4192
Publication Date
October 2008
Volume
26
Issue
8
Start / End Page
794 / 799
Location
England
Related Subject Headings
- Uracil
- Trifluridine
- Thymine
- Pyrrolidines
- Oncology & Carcinogenesis
- Neoplasms
- Middle Aged
- Maximum Tolerated Dose
- Male
- Humans
Citation
APA
Chicago
ICMJE
MLA
NLM
Overman, M. J., Kopetz, S., Varadhachary, G., Fukushima, M., Kuwata, K., Mita, A., … Abbruzzese, J. L. (2008). Phase I clinical study of three times a day oral administration of TAS-102 in patients with solid tumors. Cancer Invest, 26(8), 794–799. https://doi.org/10.1080/07357900802087242
Overman, Michael J., Scott Kopetz, Gauri Varadhachary, Masakazu Fukushima, Keizo Kuwata, Akira Mita, Robert A. Wolff, Paulo Hoff, Henry Xiong, and James L. Abbruzzese. “Phase I clinical study of three times a day oral administration of TAS-102 in patients with solid tumors.” Cancer Invest 26, no. 8 (October 2008): 794–99. https://doi.org/10.1080/07357900802087242.
Overman MJ, Kopetz S, Varadhachary G, Fukushima M, Kuwata K, Mita A, et al. Phase I clinical study of three times a day oral administration of TAS-102 in patients with solid tumors. Cancer Invest. 2008 Oct;26(8):794–9.
Overman, Michael J., et al. “Phase I clinical study of three times a day oral administration of TAS-102 in patients with solid tumors.” Cancer Invest, vol. 26, no. 8, Oct. 2008, pp. 794–99. Pubmed, doi:10.1080/07357900802087242.
Overman MJ, Kopetz S, Varadhachary G, Fukushima M, Kuwata K, Mita A, Wolff RA, Hoff P, Xiong H, Abbruzzese JL. Phase I clinical study of three times a day oral administration of TAS-102 in patients with solid tumors. Cancer Invest. 2008 Oct;26(8):794–799.
Published In
Cancer Invest
DOI
EISSN
1532-4192
Publication Date
October 2008
Volume
26
Issue
8
Start / End Page
794 / 799
Location
England
Related Subject Headings
- Uracil
- Trifluridine
- Thymine
- Pyrrolidines
- Oncology & Carcinogenesis
- Neoplasms
- Middle Aged
- Maximum Tolerated Dose
- Male
- Humans