Literature DB >> 18279578

Second-line chemotherapy use in metastatic colon cancer varies by disease responsiveness.

Seth Politano1, Michael Overman, Priyanka Pathak, Romil Chadha, Katrina Glover, David Z Chang, Robert A Wolff, Paulo M Hoff, James Abbruzzese, Cathy Eng, Scott Kopetz.   

Abstract

BACKGROUND: Improved survival of patients with metastatic colorectal cancer (CRC) has been shown to correlate with increased utilization of the 3 active cytotoxic chemotherapeutic agents: 5-fluorouracil (5-FU), irinotecan, and oxaliplatin, usually administered in 2 lines of therapy. However, it is unclear which patient, disease, and treatment characteristics are associated with the utilization of a second-line regimen. PATIENTS AND METHODS: We performed a retrospective chart review. Patients with metastatic CRC treated with bevacizumab outside of a clinical trial and any infusional 5-FU/leucovorin (LV) regimen off-protocol (ie, 5-FU/LV/irinotecan [FOLFIRI]/bevacizumab or 5-FU/LV/oxaliplatin [FOLFOX]/bevacizumab) at the University of Texas M. D. Anderson Cancer Center between February 2004 and September 2005 were included. Prespecified characteristics of age, tumor burden, severe toxicity, and front-line regimen efficacy were compared with exploratory analyses of additional patient, disease, and treatment characteristics.
RESULTS: Eighty-seven sequential patients treated with the specified front-line regimens were identified. Seventy-six percent of the eligible patients were treated with a second-line regimen. Despite equal treatment durations, patients with a better response of stable disease were significantly less likely to receive a third cytotoxic agent than patients with a partial response (68% vs. 95%; odds ratio, 8.2; P = .02) due to declining performance status (86%) or patient preference (14%). This was associated with a decreased 2-year overall survival (86% vs. 55%). Neither age, tumor burden, nor development of toxicities were associated with a different utilization of a second-line regimen.
CONCLUSION: Failure to obtain a response to initial chemotherapy for metastatic disease appears to be associated with decreased utilization of a second-line regimen.

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Year:  2008        PMID: 18279578     DOI: 10.3816/CCC.2008.n.008

Source DB:  PubMed          Journal:  Clin Colorectal Cancer        ISSN: 1533-0028            Impact factor:   4.481


  4 in total

1.  Caspase-mediated pro-apoptotic interaction of panaxadiol and irinotecan in human colorectal cancer cells.

Authors:  Guang-Jian Du; Chong-Zhi Wang; Zhi-Yu Zhang; Xiao-Dong Wen; Jacqueline Somogyi; Tyler Calway; Tong-Chuan He; Wei Du; Chun-Su Yuan
Journal:  J Pharm Pharmacol       Date:  2012-02-21       Impact factor: 3.765

2.  Phase II trial of infusional fluorouracil, irinotecan, and bevacizumab for metastatic colorectal cancer: efficacy and circulating angiogenic biomarkers associated with therapeutic resistance.

Authors:  Scott Kopetz; Paulo M Hoff; Jeffrey S Morris; Robert A Wolff; Cathy Eng; Katrina Y Glover; Rosie Adinin; Michael J Overman; Vincete Valero; Sijin Wen; Christopher Lieu; Shaoyu Yan; Hai T Tran; Lee M Ellis; James L Abbruzzese; John V Heymach
Journal:  J Clin Oncol       Date:  2009-12-14       Impact factor: 44.544

3.  Angiogenesis-related protein expression in bevacizumab-treated metastatic colorectal cancer: NOTCH1 detrimental to overall survival.

Authors:  Tadeu Ferreira Paiva; Victor Hugo Fonseca de Jesus; Raul Amorim Marques; Alexandre André Balieiro Anastácio da Costa; Mariana Petaccia de Macedo; Patricia Maria Peresi; Aline Damascena; Benedito Mauro Rossi; Maria Dirlei Begnami; Vladmir Cláudio Cordeiro de Lima
Journal:  BMC Cancer       Date:  2015-09-22       Impact factor: 4.430

4.  Does the type of first-line regimens influence the receipt of second-line chemotherapy treatment? An analysis of 3211 metastatic colon cancer patients.

Authors:  Zhiyuan Zheng; Nader Hanna; Eberechukwu Onukwugha; Emily S Reese; Brian Seal; C Daniel Mullins
Journal:  Cancer Med       Date:  2014-01-07       Impact factor: 4.452

  4 in total

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