Literature DB >> 12941200

Colorectal cancer: integrating oxaliplatin.

Christophe Louvet1, Aimery de Gramont.   

Abstract

5-Fluorouracil (5-FU), used according to several types of administration and several modulations, remained the standard treatment of colorectal cancer for many years. However, two major drugs (irinotecan and oxaliplatin) improved the therapeutic possibilities for this disease. Both drugs are active as a single agent, but they have a clear in vitro and in vivo synergistic antitumoral activity when combined with modulated 5-FU. Significant improvements in response rate, progression-free survival, and overall survival have been obtained by irinotecan/5-FU and oxaliplatin/5-FU combinations compared to 5-FU alone. Integrating these drugs in the therapeutic strategy of metastatic colorectal cancer treatment was a challenge for clinical trials. Second- and third-line treatments are often used, and these treatments are a large reason for the improvement in survival. Each patient who is able to receive several lines of therapy should be offered this strategy. Many attempts to optimize the results of these combinations have been performed. Although no definitive data show one drug to be better than the other, several arguments favored the oxaliplatin/5-FU combination as a first-line treatment of metastatic colorectal cancer. A better collaboration between surgeons and oncologists, based on the improvement of surgical techniques and highly active chemotherapeutic regimens, provides patients more strategies with curative intent in liver and lung metastatic disease. Progress in treating metastatic disease will hopefully translate into the improvement of cure rates when applied to adjuvant therapy. The tolerance of the oxaliplatin/5-FU combination allows for design regimens integrating new drugs, such as biologic modifiers.

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Year:  2003        PMID: 12941200     DOI: 10.1007/s11864-003-0041-8

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  10 in total

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9.  High-dose intensity oxaliplatin added to the simplified bimonthly leucovorin and 5-fluorouracil regimen as second-line therapy for metastatic colorectal cancer (FOLFOX 7).

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Journal:  Eur J Cancer       Date:  2001-05       Impact factor: 9.162

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Journal:  J Clin Oncol       Date:  1998-08       Impact factor: 44.544

  10 in total
  5 in total

1.  Inhibition of NF-kappaB signaling by quinacrine is cytotoxic to human colon carcinoma cell lines and is synergistic in combination with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) or oxaliplatin.

Authors:  Tanvi S Jani; Jennifer DeVecchio; Tapati Mazumdar; Akwasi Agyeman; Janet A Houghton
Journal:  J Biol Chem       Date:  2010-04-27       Impact factor: 5.157

2.  Early effects of FOLFOX treatment of colorectal tumour in an animal model: assessment of changes in gene expression and FDG kinetics.

Authors:  Ludwig G Strauss; Johannes Hoffend; Dirk Koczan; Leyun Pan; Uwe Haberkorn; Antonia Dimitrakopoulou-Strauss
Journal:  Eur J Nucl Med Mol Imaging       Date:  2009-03-11       Impact factor: 9.236

3.  Novel Rhodanine Derivative, 5-[4-(4-Fluorophenoxy) phenyl]methylene-3-{4-[3-(4-methylpiperazin-1-yl) propoxy]phenyl}-2-thioxo-4-thiazolidinone dihydrochloride, Induces Apoptosis via Mitochondria Dysfunction and Endoplasmic Reticulum Stress in Human Colon Cancer Cells.

Authors:  Hye-Uk Jung; Jeong-Hun Lee; Kyung-Sook Chung; Joo Young Hong; Jung-Hye Choi; Soo-Dong Kim; Eun Joo Roh; Kye Jung Shin; Kyung-Tae Lee
Journal:  Molecules       Date:  2018-11-06       Impact factor: 4.411

4.  Phase II study of UFT and oxaliplatin in first-line treatment of advanced colorectal cancer.

Authors:  J Feliu; J M Vicent; C García-Girón; M Constela; E Fonseca; J Aparicio; M Lomas; L Antón-Aparicio; F J Dorta; M Gonzalez-Baron
Journal:  Br J Cancer       Date:  2004-11-15       Impact factor: 7.640

5.  Selective Internal Radiation Therapy (SIRT) with yttrium-90 resin microspheres plus standard systemic chemotherapy regimen of FOLFOX versus FOLFOX alone as first-line treatment of non-resectable liver metastases from colorectal cancer: the SIRFLOX study.

Authors:  Peter Gibbs; Val Gebski; Mark Van Buskirk; Kenneth Thurston; David N Cade; Guy A Van Hazel
Journal:  BMC Cancer       Date:  2014-12-01       Impact factor: 4.430

  5 in total

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