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Molecular and Clinical Oncology
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September-October 2014 Volume 2 Issue 5

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International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

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International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

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Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

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Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

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Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

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Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

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Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

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Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

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Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

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Article

XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI

  • Authors:
    • Koichi Suzuki
    • Kato Takaharu
    • Yuta Muto
    • Kosuke Ichida
    • Taro Fukui
    • Yuji Takayama
    • Shingo Tsujinaka
    • Junichi Sasaki
    • Hisanaga Horie
    • Yutaka J. Kawamura
    • Fumio Konishi
    • Toshiki Rikiyama
  • View Affiliations / Copyright

    Affiliations: Department of Surgery, Saitama Medical Center, Jichi Medical University, Saitama 330‑8503, Japan, Nerima‑Hikarigaoka Hospital, Tokyo 179‑0072, Japan
  • Pages: 827-832
    |
    Published online on: June 6, 2014
       https://doi.org/10.3892/mco.2014.306
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Abstract

The aim of the present study was to present a retrospective review of 42 metastatic colorectal cancer (mCRC) patients treated using the XELIRI regimen as second‑line chemotherapy during the period between 2010 and 2012. Patients were treated with capecitabine, 1,600 (≥65 years) or 2,000 mg/m2 (<65 years), on days 1‑15, 200 mg/m2 irinotecan (CPT‑11) on day 1, with or without 7.5 mg/kg bevacizumab on day 1 and every 21 days. A total of 21 patients underwent XELIRI and 21 underwent XELIRI plus bevacizumab treatment. Fifteen patients received continuous administration of bevacizumab in the first‑ and second‑line settings [bevacizumab beyond progression (BBP)+], whereas 27 patients did not receive the treatment (BBP‑). Forty patients (95.2%), including all the patients in the BBP+ group, received sequentially administered XELOX and XELIRI regimens from the first‑ to the second‑line setting. The disease control rate (DCR), progression‑free survival (PFS), overall survival (OS) and adverse events were compared between the BBP‑ and BBP+ groups. The median relative dose intensity was similar (93.9% for capecitabine and 96.3% for CPT‑11 in the BBP‑ group vs. 94.8% for capecitabine and 91.5% for CPT‑11 in the BBP+ group). The DCR was 25.9% in the BBP‑ and 66.6% in the BBP+ groups (P=0.020). The median PFS was 3.5 months in the BBP‑ and 7.2 months in the BBP+ groups (P=0.028). The BBP+ group exhibited a higher median OS time compared to the BBP‑ group (12.5 months in the BBP‑ group vs. not reached in the BBP+ group; P=0.0267). The most common grade 3/4 adverse event (n≥20) was hypertension observed in the BBP+ group [three patients (20%)]: these three patients were well‑controlled with a single antihypertensive drug. Treatment with sequentially administered XELOX and XELIRI regimens did not aggravate adverse events in the 40 patients. The results showed that the XELIRI regimen, involving continuous treatment with bevacizumab, was well‑tolerated and effective as a second‑line chemotherapy and sequentially administering XELOX and XELIRI was feasible and manageable for patients with mCRC.
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Copy and paste a formatted citation
Spandidos Publications style
Suzuki K, Takaharu K, Muto Y, Ichida K, Fukui T, Takayama Y, Tsujinaka S, Sasaki J, Horie H, Kawamura YJ, Kawamura YJ, et al: XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI. Mol Clin Oncol 2: 827-832, 2014.
APA
Suzuki, K., Takaharu, K., Muto, Y., Ichida, K., Fukui, T., Takayama, Y. ... Rikiyama, T. (2014). XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI. Molecular and Clinical Oncology, 2, 827-832. https://doi.org/10.3892/mco.2014.306
MLA
Suzuki, K., Takaharu, K., Muto, Y., Ichida, K., Fukui, T., Takayama, Y., Tsujinaka, S., Sasaki, J., Horie, H., Kawamura, Y. J., Konishi, F., Rikiyama, T."XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI". Molecular and Clinical Oncology 2.5 (2014): 827-832.
Chicago
Suzuki, K., Takaharu, K., Muto, Y., Ichida, K., Fukui, T., Takayama, Y., Tsujinaka, S., Sasaki, J., Horie, H., Kawamura, Y. J., Konishi, F., Rikiyama, T."XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI". Molecular and Clinical Oncology 2, no. 5 (2014): 827-832. https://doi.org/10.3892/mco.2014.306
Copy and paste a formatted citation
x
Spandidos Publications style
Suzuki K, Takaharu K, Muto Y, Ichida K, Fukui T, Takayama Y, Tsujinaka S, Sasaki J, Horie H, Kawamura YJ, Kawamura YJ, et al: XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI. Mol Clin Oncol 2: 827-832, 2014.
APA
Suzuki, K., Takaharu, K., Muto, Y., Ichida, K., Fukui, T., Takayama, Y. ... Rikiyama, T. (2014). XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI. Molecular and Clinical Oncology, 2, 827-832. https://doi.org/10.3892/mco.2014.306
MLA
Suzuki, K., Takaharu, K., Muto, Y., Ichida, K., Fukui, T., Takayama, Y., Tsujinaka, S., Sasaki, J., Horie, H., Kawamura, Y. J., Konishi, F., Rikiyama, T."XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI". Molecular and Clinical Oncology 2.5 (2014): 827-832.
Chicago
Suzuki, K., Takaharu, K., Muto, Y., Ichida, K., Fukui, T., Takayama, Y., Tsujinaka, S., Sasaki, J., Horie, H., Kawamura, Y. J., Konishi, F., Rikiyama, T."XELIRI regimen plus continuous treatment with bevacizumab is well-tolerated and effective in metastatic colorectal cancer patients in a second‑line setting involving the sequential administration of XELOX and XELIRI". Molecular and Clinical Oncology 2, no. 5 (2014): 827-832. https://doi.org/10.3892/mco.2014.306
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