Literature DB >> 23558559

Feasibility and pharmacokinetics of combined therapy with S-1 and trastuzumab in patients with human epidermal growth factor receptor 2-positive metastatic or recurrent breast cancer.

Yasuhiro Suzuki1, Rin Ogiya, Risa Oshitanai, Mayako Terao, Mizuho Terada, Toru Morioka, Banri Tsuda, Naoki Niikura, Takuho Okamura, Yuki Saito, Yutaka Tokuda.   

Abstract

BACKGROUND: To clarify the tolerance and pharmacokinetics of combined therapy with S-1 and trastuzumab in patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic or recurrent breast cancer.
METHODS: From January 2008 through to September 2009, combined therapy with S-1 and trastuzumab was given to 7 patients with HER2-positive metastatic or recurrent breast cancer. The incidence of adverse events and the pharmacokinetics of tegafur, 5-fluorouracil, and gimeracil in plasma were studied.
RESULTS: One patient had grade 3 leukopenia, and another had a grade 3 elevation of alanine aminotransferase. All other adverse events were grade 2 or lower. The combination of S-1 and trastuzumab did not cause any new adverse events. The incidence of adverse events was similar to those associated with S-1 alone. The median number of treatment cycles was 11. The pharmacokinetics of tegafur, 5-fluorouracil, and gimeracil after treatment with S-1 plus trastuzumab did not markedly differ from those after S-1 alone.
CONCLUSIONS: Combined therapy with S-1 and trastuzumab did not cause any new adverse events, administration continuity was good, and the therapy was well tolerated.

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Year:  2013        PMID: 23558559     DOI: 10.1007/s10147-013-0547-4

Source DB:  PubMed          Journal:  Int J Clin Oncol        ISSN: 1341-9625            Impact factor:   3.402


  17 in total

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Journal:  Anticancer Res       Date:  2011-09       Impact factor: 2.480

3.  Determination of S-1 (combined drug of tegafur, 5-chloro-2,4-dihydroxypyridine and potassium oxonate) and 5-fluorouracil in human plasma and urine using high-performance liquid chromatography and gas chromatography-negative ion chemical ionization mass spectrometry.

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5.  A phase I/II trial of trastuzumab plus erlotinib in metastatic HER2-positive breast cancer: a dual ErbB targeted approach.

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7.  Pharmacokinetics, safety, and efficacy of trastuzumab administered every three weeks in combination with paclitaxel.

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Journal:  J Clin Oncol       Date:  2003-09-24       Impact factor: 44.544

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  3 in total

1.  Phase II multi-center clinical study on using S-1 to treat advanced breast cancer after resistance to anthracycline and taxane drugs in Chinese patients.

Authors:  Peng Yuan; Li-Jun Di; Wei Liu; Dong-Gui Wan; Hong Dai; Zhong-Sheng Tong; Feng Du; Bing-He Xu
Journal:  Int J Clin Exp Med       Date:  2015-02-15

2.  Evaluation of Left Ventricular Ejection Fractions in Breast Cancer Patients Undergoing Long-Term Trastuzumab Treatment.

Authors:  Yong Sun; Tao Li; Yuanpeng Zhang; Qiwen Zhang
Journal:  Med Sci Monit       Date:  2016-12-21

3.  Phase II study of sequential S-1 and cyclophosphamide therapy in patients with metastatic breast cancer.

Authors:  Keiko Yanai; Takaaki Fujii; Jun Horiguchi; Yuko Nakazawa; Sasagu Kurozumi; Sayaka Obayashi; Reina Yajima; Ken Shirabe
Journal:  BMC Cancer       Date:  2020-11-06       Impact factor: 4.430

  3 in total

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