Literature DB >> 27091467

The Best. First. Anti-EGFR before anti-VEGF, in the first-line treatment of RAS wild-type metastatic colorectal cancer: from bench to bedside.

A Zaniboni1, V Formica2.   

Abstract

BACKGROUND: Since 2013, informative trials exploring the optimal use of available biologic agents in the first-line setting of metastatic colorectal cancer (mCRC) have been presented. These trials have opened a stimulating debate on the biological effect that first-line therapies may have on subsequent lines of treatment even long after the first-line progression.
MATERIALS AND METHODS: We reviewed available preclinical and clinical data on the effect of different sequences of the biological drugs approved for use in mCRC patients. The importance of molecular selection of patients based on RAS mutational status and toxicity and quality-of-life issues were also analyzed.
RESULTS: Convincing evidence exists on the optimal therapeutic effect obtained by using anti-EGFR agents in first-line treatment before anti-VEGF agents. On the contrary, up-front anti-VEGF agents' use seems to determine biological changes that increase the risk of acquired resistance to subsequent EGFR inhibitors. This hypothesis is confirmed by the scarce evidence of EGFR inhibitor activity in second-line treatment. Such a therapeutic optimum is subject to a fine molecular selection based on RAS mutational status.
CONCLUSION: There is accumulating evidence suggesting that, after precise and well-established molecular selection, anti-EGFR agents deliver their maximum efficacy in mCRC patients when given early in the treatment strategy. Their toxicity profile seems manageable under the supervision of experienced physicians. Large randomized trials prospectively confirming the impact of different sequencing strategies are eagerly awaited.

Entities:  

Keywords:  Anti-EGFR therapy; Bevacizumab; Cetuximab; Colon cancer; Panitumumab; Sequential treatment

Mesh:

Substances:

Year:  2016        PMID: 27091467     DOI: 10.1007/s00280-016-3032-8

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  18 in total

1.  Continuation of Bevacizumab vs Cetuximab Plus Chemotherapy After First Progression in KRAS Wild-Type Metastatic Colorectal Cancer: The UNICANCER PRODIGE18 Randomized Clinical Trial.

Authors:  Jaafar Bennouna; Sandrine Hiret; Aurelie Bertaut; Olivier Bouché; Gael Deplanque; Christian Borel; Eric François; Thierry Conroy; François Ghiringhelli; Gaëtan des Guetz; Jean-François Seitz; Pascal Artru; Mohamed Hebbar; Trevor Stanbury; Marc G Denis; Antoine Adenis; Christophe Borg
Journal:  JAMA Oncol       Date:  2019-01-01       Impact factor: 31.777

2.  KRAS and BRAF Mutations in Stage II and III Colon Cancer: A Systematic Review and Meta-Analysis.

Authors:  Vincenzo Formica; Francesco Sera; Chiara Cremolini; Silvia Riondino; Cristina Morelli; Hendrik-Tobias Arkenau; Mario Roselli
Journal:  J Natl Cancer Inst       Date:  2022-04-11       Impact factor: 11.816

3.  Exploratory pooled analysis evaluating the effect of sequence of biological therapies on overall survival in patients with RAS wild-type metastatic colorectal carcinoma.

Authors:  Marc Peeters; Frédéric Forget; Meinolf Karthaus; Manuel Valladares-Ayerbes; Alberto Zaniboni; Gaston Demonty; Xuesong Guan; Fernando Rivera
Journal:  ESMO Open       Date:  2018-02-24

4.  Combined application of anti-VEGF and anti-EGFR attenuates the growth and angiogenesis of colorectal cancer mainly through suppressing AKT and ERK signaling in mice model.

Authors:  Chenbo Ding; Longmei Li; Taoyu Yang; Xiaobo Fan; Guoqiu Wu
Journal:  BMC Cancer       Date:  2016-10-12       Impact factor: 4.430

Review 5.  Optimizing the use of anti VEGF targeted therapies in patients with metastatic colorectal cancer: review of literature.

Authors:  Claudiu Hopirtean; Viorica Nagy
Journal:  Clujul Med       Date:  2018-01-15

6.  Biologic Response of Colorectal Cancer Xenograft Tumors to Sequential Treatment with Panitumumab and Bevacizumab.

Authors:  Hiroya Taniguchi; Yuji Baba; Yoji Sagiya; Masamitsu Gotou; Kazuhide Nakamura; Hiroshi Sawada; Kazunori Yamanaka; Yukiko Sakakibara; Ikuo Mori; Yukiko Hikichi; Junpei Soeda; Hideo Baba
Journal:  Neoplasia       Date:  2018-05-23       Impact factor: 5.715

7.  Anti-VEGF and anti-EGFR agents open up new horizons changing the landscape for their associations.

Authors:  Gerard Milano
Journal:  Cancer Chemother Pharmacol       Date:  2016-06-16       Impact factor: 3.333

8.  Distinct effects of EGFR inhibitors on epithelial- and mesenchymal-like esophageal squamous cell carcinoma cells.

Authors:  Masahiro Yoshioka; Shinya Ohashi; Tomomi Ida; Yukie Nakai; Osamu Kikuchi; Yusuke Amanuma; Junichi Matsubara; Atsushi Yamada; Shin'ichi Miyamoto; Mitsuteru Natsuizaka; Hiroshi Nakagawa; Tsutomu Chiba; Hiroshi Seno; Manabu Muto
Journal:  J Exp Clin Cancer Res       Date:  2017-08-01

9.  Oral mucositis associated with anti-EGFR therapy in colorectal cancer: single institutional retrospective cohort study.

Authors:  Satoshi Dote; Shoji Itakura; Kohei Kamei; Daiki Hira; Satoshi Noda; Yuka Kobayashi; Tomohiro Terada
Journal:  BMC Cancer       Date:  2018-10-05       Impact factor: 4.430

10.  Relationships between tumour response and primary tumour location, and predictors of long-term survival, in patients with RAS wild-type metastatic colorectal cancer receiving first-line panitumumab therapy: retrospective analyses of the PRIME and PEAK clinical trials.

Authors:  Marc Peeters; Timothy Price; Julien Taieb; Michael Geissler; Fernando Rivera; Jean-Luc Canon; George Pentheroudakis; Reija Koukakis; Peter Burdon; Salvatore Siena
Journal:  Br J Cancer       Date:  2018-07-17       Impact factor: 7.640

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