Literature DB >> 15719490

Phase I study of concomitant chemoradiation with raltitrexed in locally advanced head and neck cancer.

A Planting1, M de Jong, P Jansen, J Kerrebijn, M Smith, J Verweij.   

Abstract

In patients with non-resectable head and neck cancer concomitant chemoradiotherapy is increasingly used, especially in cases of oropharyngeal and hypopharyngeal tumours. Most chemoradiotherapy regimes contain cisplatin as a single agent or in combination with fluorouracil. However, not all patients are fit enough for a cisplatin-containing regime or they refuse hospital admission. Raltitrexed is a specific thymidylate synthase inhibitor that has been studied as a radiosensitiser in rectal cancer. Raltitrexed can be administered easily in an outpatient setting and has few short-term effects. We studied raltitrexed at escalating doses combined with standard radiotherapy in advanced head and neck cancer patients. Seventeen patients with locally advanced head and neck cancers were enrolled in the study. Raltitrexed was administered at dose levels of 1.5, 2.0, 2.5 and 3.0 mg/m(2) intravenously (i.v), once every 3 weeks, for two doses. Radiotherapy consisted of 70 Gy given over 7 weeks in five fractions of 2 Gy per week. In general, treatment toxicity (DLT), complicated febrile neutropenia, was observed at 3.0 mg/m(2) in two of four patients. The dose of 2.5 mg/m(2) was extended thereafter with additional patients without major toxicity. Radiotherapy had to be interrupted in one patient. Five patients had a clinical complete response(CR) and eleven a partial response (PR) six weeks after the last fraction of radiotherapy. Twelve out of 17 patients remained free of locoregional recurrence after a median follow-up of 24(+) months (range 3-60+ months). Raltitrexed, at a dose of 2.5 mg/m(2) given twice 3 weeks apart, can be administered in combination with 70 Gy of radiotherapy in locally advanced head and neck cancer patients with a manageable tolerability profile. The clinical results and convenience of the schedule make raltitrexed an attractive drug to explore further in patients considered unfit for cisplatin-containing chemoradiation regimens.

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Year:  2005        PMID: 15719490     DOI: 10.1016/j.ejca.2004.09.022

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  4 in total

1.  Phase II study of induction chemotherapy followed by concurrent chemoradiotherapy with raltitrexed and cisplatin in locally advanced nasopharyngeal carcinoma.

Authors:  Yuan Wu; Xueyan Wei; Zilong Yuan; Hongbin Xu; Yanping Li; Ying Li; Liu Hu; Guang Han; Yu Qian; Desheng Hu
Journal:  Chin J Cancer Res       Date:  2020-10-31       Impact factor: 5.087

2.  Raltitrexed Enhances the Antitumor Effect of Apatinib in Human Esophageal Squamous Carcinoma Cells via Akt and Erk Pathways.

Authors:  Hongchao Zhen; Guangxin Li; Pengfei Zhao; Ying Zhang; Jing Wang; Junxian Yu; Bangwei Cao
Journal:  Onco Targets Ther       Date:  2020-12-01       Impact factor: 4.147

3.  Raltitrexed increases radiation sensitivity of esophageal squamous carcinoma cells.

Authors:  Wen-Xiu Ding; Shu Liu; Jian-Xin Ma; Juan Pu; Hai-Jing Wang; Shu Zhang; Xin-Chen Sun
Journal:  Cancer Cell Int       Date:  2019-02-18       Impact factor: 5.722

4.  The Frequency of Circulating Tumour Cells and the Correlation with the Clinical Response to Standard Chemoradiotherapy in Locally Advanced Nasopharyngeal Carcinoma: A Prospective Study.

Authors:  Yu Qian; Yuan Wu; Zilong Yuan; Xiaohui Niu; Yaoyao He; Jun Peng; Fuxiang Zhou; Shaozhong Wei; Desheng Hu; Yunfeng Zhou
Journal:  Cancer Manag Res       Date:  2019-12-02       Impact factor: 3.989

  4 in total

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