Literature DB >> 18477855

XELOX followed by XELIRI or the reverse sequence in advanced colorectal cancer.

B Sakar1, M Gumus, M Basaran, A Argon, Z Ustuner, M A Ustaoglu, S Saglam, N Guney, A N Tenekeci, N F Aykan.   

Abstract

BACKGROUND: Capecitabine has demonstrated high efficacy as first-line treatment for metastatic colorectal cancer (mCRC). In this non-randomized pilot study, we investigated the efficacy and safety of sequentially administered XELOX and XELIRI regimens or the reverse sequence in patients with advanced colorectal cancer. PATIENTS AND METHODS: Entry criteria were histologically confirmed mCRC, ECOG performance status (PS) < or =2 and adequate bone marrow, renal and hepatic function. All patients consecutively received XELOX followed by XELIRI at disease progression or vice versa.
RESULTS: In multivariate analysis, independent prognostic factors with worse overall survival were: lower PS (p = 0.0001), multiple metastatic sites (p = 0.016) and high tumor grade. Higher serum levels of alkaline phosphatase and worse ECOG PS were associated with a shorter progression-free survival. Grade 3/4 mucositis, nausea/vomiting, grade 3/4 alopecia and grade 3 diarrhea were more frequent with XELIRI, whereas major toxicity events with XELOX were grade 3 neutropenia, thrombocytopenia and grade 2/3 neurotoxicity.
CONCLUSION: Capecitabine appears to be an acceptable alternative to continuous-infusion fluorouracil (FU)/leucovorin (LV) in combination therapy and offers an effective, but more convenient alternative to continuous infusion FU/LV in the first-line treatment of patients with mCRC. 2008 S. Karger AG, Basel.

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Year:  2008        PMID: 18477855     DOI: 10.1159/000132395

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  2 in total

1.  Sequential administration of XELOX and XELIRI is effective, feasible and well tolerated by patients with metastatic colorectal cancer.

Authors:  Taro Fukui; Koichi Suzuki; Kosuke Ichida; Yuji Takayama; Nao Kakizawa; Yuta Muto; Fumi Hasegawa; Fumiaki Watanabe; Rina Kikugawa; Masaaki Saito; Shingo Tsujinaka; Yasuyuki Miyakura; Toshiki Rikiyama
Journal:  Oncol Lett       Date:  2017-04-26       Impact factor: 2.967

2.  Examination of multiple UGT1A and DPYD polymorphisms has limited ability to predict the toxicity and efficacy of metastatic colorectal cancer treated with irinotecan-based chemotherapy: a retrospective analysis.

Authors:  Dan Liu; Jian Li; Jing Gao; Yanyan Li; Rui Yang; Lin Shen
Journal:  BMC Cancer       Date:  2017-06-20       Impact factor: 4.430

  2 in total

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