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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

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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