Literature DB >> 17536342

Optimizing palliative treatment of metastatic colorectal cancer in the era of biologic therapy.

Axel Grothey1, John L Marshall.   

Abstract

Over the past decade, new cytotoxic and biologic therapies beyond the old standard-of-care, biomodulated fluorouracil (5-FU), have become available for the treatment of metastatic colorectal cancer (mCRC). The introductions of irinotecan (Camptosar), oxaliplatin (Eloxatin), and bevacizumab (Avastin) have prolonged survival, but the optimal use of these new therapies remains to be determined. Issues remain regarding management of toxicities, treatment of elderly patients or those with poor performance status, and the duration of treatment with front-line therapy. This article reviews recent and ongoing studies of newer therapies in an effort to determine the best use of these drugs in the treatment of mCRC. Current data support the front-line use of bevacizumab added to either 5-FU/leucovorin alone or 5-FU/leucovorin in combination with oxaliplatin (FOLFOX/bevacizumab) or irinotecan (FOLFIRI/bevacizumab). If oxaliplatin is used in first-line therapy, oxaliplatin should be discontinued before the development of severe neurotoxicity and be reintroduced or replaced with irinotecan on disease progression. Definitive conclusions on the sequence and duration of front-line therapy and the most effective strategy to ameliorate toxicity await results of ongoing prospective clinical trials.

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Year:  2007        PMID: 17536342

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN: 0890-9091            Impact factor:   2.990


  7 in total

1.  EGFR gene copy number as a predictive biomarker for resistance to anti-EGFR monoclonal antibodies in metastatic colorectal cancer treatment: a meta-analysis.

Authors:  Wei-Dong Shen; Hong-Lin Chen; Peng-Fei Liu
Journal:  Chin J Cancer Res       Date:  2014-02       Impact factor: 5.087

2.  Annual report to the nation on the status of cancer, 1975-2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates.

Authors:  Brenda K Edwards; Elizabeth Ward; Betsy A Kohler; Christie Eheman; Ann G Zauber; Robert N Anderson; Ahmedin Jemal; Maria J Schymura; Iris Lansdorp-Vogelaar; Laura C Seeff; Marjolein van Ballegooijen; S Luuk Goede; Lynn A G Ries
Journal:  Cancer       Date:  2010-02-01       Impact factor: 6.860

3.  Outcomes for Metastatic Colorectal Cancer Based on Microsatellite Instability: Results from the South Australian Metastatic Colorectal Cancer Registry.

Authors:  Li Chia Chong; Amanda Rose Townsend; Joanne Young; Amitesh Roy; Cynthia Piantadosi; Jennifer E Hardingham; David Roder; Christos Karapetis; Robert Padbury; Guy Maddern; James Moore; Timothy Jay Price
Journal:  Target Oncol       Date:  2019-02       Impact factor: 4.493

4.  Medical treatment of advanced colorectal cancer in 2009.

Authors:  Axel Grothey
Journal:  Ther Adv Med Oncol       Date:  2009-09       Impact factor: 8.168

Review 5.  Irinotecan as palliative chemotherapy for metastatic colorectal cancer: evolving tactics following initial treatment.

Authors:  Emmanuel Mitry; Astrid Lièvre; Jean-Baptiste Bachet; Philippe Rougier
Journal:  Int J Colorectal Dis       Date:  2009-02-17       Impact factor: 2.571

6.  Mucinous histology predicts for poor response rate and overall survival of patients with colorectal cancer and treated with first-line oxaliplatin- and/or irinotecan-based chemotherapy.

Authors:  V Catalano; F Loupakis; F Graziano; U Torresi; R Bisonni; D Mari; L Fornaro; A M Baldelli; P Giordani; D Rossi; P Alessandroni; L Giustini; R R Silva; A Falcone; S D'Emidio; S L Fedeli
Journal:  Br J Cancer       Date:  2009-03-03       Impact factor: 7.640

Review 7.  Advances in immunotherapy for colorectal cancer: a review.

Authors:  Gol Golshani; Yue Zhang
Journal:  Therap Adv Gastroenterol       Date:  2020-06-01       Impact factor: 4.409

  7 in total

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