Literature DB >> 21447970

Reintroduction of oxaliplatin: a viable approach to the long-term management of metastatic colorectal cancer.

Axel Grothey1.   

Abstract

Oxaliplatin-based chemotherapy is an effective first-line treatment option for patients with metastatic colorectal cancer (mCRC), which, in combination with targeted therapies and a sequential treatment approach using all active agents, has extended median overall survival to 2 years and beyond. Prolonged survival brings into focus the burden of treatment, in terms of associated toxicities and quality of life, and attention is now being paid to lowering the toxicity burden for patients receiving chemotherapy for mCRC without compromising efficacy. The use of oxaliplatin can lead to the development of sensory neuropathy, which commonly limits the dose and/or duration of treatment that can be administered. Temporary withdrawal of oxaliplatin (treatment holidays) has been shown to be an effective strategy for the management of this adverse effect. Data from randomized controlled trials indicate that a formalized stop-and-go approach to the delivery of oxaliplatin does not compromise efficacy, and indeed for some patients may prove beneficial by allowing them to continue treatment for longer periods. This paper presents a critical review of the evidence to support the utility of treatment interruption and reintroduction of oxaliplatin for the long-term management of mCRC.
Copyright © 2011 S. Karger AG, Basel.

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Year:  2011        PMID: 21447970     DOI: 10.1159/000323491

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


  5 in total

1.  Multicenter randomized phase II clinical trial of oxaliplatin reintroduction as a third- or later-line therapy for metastatic colorectal cancer-biweekly versus standard triweekly XELOX (The ORION Study).

Authors:  Chu Matsuda; Michitaka Honda; Chihiro Tanaka; Mutsumi Fukunaga; Keiichiro Ishibashi; Yoshinori Munemoto; Taishi Hata; Hiroyuki Bando; Mitsuru Oshiro; Michiya Kobayashi; Yukihiko Tokunaga; Akitomo Fujii; Naoki Nagata; Koji Oba; Hideyuki Mishima
Journal:  Int J Clin Oncol       Date:  2015-10-16       Impact factor: 3.402

Review 2.  Drug rechallenge and treatment beyond progression--implications for drug resistance.

Authors:  Elizabeth A Kuczynski; Daniel J Sargent; Axel Grothey; Robert S Kerbel
Journal:  Nat Rev Clin Oncol       Date:  2013-09-03       Impact factor: 66.675

3.  Spinal astrocyte gap junctions contribute to oxaliplatin-induced mechanical hypersensitivity.

Authors:  Seo-Yeon Yoon; Caleb R Robinson; Haijun Zhang; Patrick M Dougherty
Journal:  J Pain       Date:  2013-02       Impact factor: 5.820

4.  Prechemotherapy Touch Sensation Deficits Predict Oxaliplatin-Induced Neuropathy in Patients with Colorectal Cancer.

Authors:  Xin Shelley Wang; Qiuling Shi; Patrick M Dougherty; Cathy Eng; Tito R Mendoza; Loretta A Williams; David R Fogelman; Charles S Cleeland
Journal:  Oncology       Date:  2016-02-17       Impact factor: 2.935

5.  Autophagy protects against oxaliplatin-induced cell death via ER stress and ROS in Caco-2 cells.

Authors:  Yan Shi; Bin Tang; Pei-Wu Yu; Bo Tang; Ying-Xue Hao; Xiao Lei; Hua-Xing Luo; Dong-Zhu Zeng
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

  5 in total

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