Literature DB >> 25958297

Bevacizumab-based neoadjuvant chemotherapy for colorectal cancer liver metastases: Pitfalls and helpful tricks in a review for clinicians.

Filippo Pietrantonio1, Armando Orlandi2, Alessandro Inno3, Valentina Da Prat4, Daniele Spada5, Alessandro Iaculli6, Maria Di Bartolomeo4, Carlo Morosi7, Filippo de Braud4.   

Abstract

Bevacizumab added to chemotherapy has shown encouraging efficacy in the neoadjuvant therapy of colorectal cancer liver metastases. In absence of biological predictor factors of efficacy to bevacizumab-based treatment, the assessment of response may be a crucial point to select patients who may benefit the most from surgery. At the same time the pathological response after liver resection could represent a guide for the next therapeutic plan. In the pre-surgical phase, conventional computed tomography and response evaluation with RECIST criteria may underestimate the response to anti-angiogenic drugs. Modified computed tomography criteria of response, morphologic changes as well as novel imaging techniques and metabolic assessment by fluorodeoxyglucose positron emission tomography seem to be promising methods for the assessment of response and for leading the clinical choices. Pathological response at the time of surgery is an important prognostic factor and a surrogate of survival for resected patients. Different classification criteria to assess pathological response have been developed, residual viable tumor, tumor regression grade (TRG), modified TRG and tumor thickness at the tumor-normal interface, but to date a superiority of one approach over the others has not been clearly established. In this review, we evaluate the available data with the aim to help the clinicians in the pre- and post-surgical care of patient with colorectal cancer liver metastases treated with bevacizumab-based neoadjuvant strategy.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Bevacizumab; Colorectal cancer; Liver metastases; Neoadjuvant; Response criteria

Mesh:

Substances:

Year:  2015        PMID: 25958297     DOI: 10.1016/j.critrevonc.2015.04.008

Source DB:  PubMed          Journal:  Crit Rev Oncol Hematol        ISSN: 1040-8428            Impact factor:   6.312


  6 in total

1.  Pathological response after neoadjuvant bevacizumab- or cetuximab-based chemotherapy in resected colorectal cancer liver metastases.

Authors:  Filippo Pietrantonio; Vincenzo Mazzaferro; Rosalba Miceli; Christian Cotsoglou; Flavia Melotti; Giuseppe Fanetti; Federica Perrone; Pamela Biondani; Cecilia Muscarà; Maria Di Bartolomeo; Jorgelina Coppa; Claudia Maggi; Massimo Milione; Elena Tamborini; Filippo de Braud
Journal:  Med Oncol       Date:  2015-05-24       Impact factor: 3.064

Review 2.  Clinical trials of antiangiogenic therapy for hepatocellular carcinoma.

Authors:  Akinobu Taketomi
Journal:  Int J Clin Oncol       Date:  2016-02-22       Impact factor: 3.402

3.  Maximum Diameter and Number of Tumors as a New Prognostic Indicator of Colorectal Liver Metastases.

Authors:  Toshiaki Yoshimoto; Yuji Morine; Satoru Imura; Tetsuya Ikemoto; Syuichi Iwahashi; Y U Saito; Sinichiro Yamada; Daichi Ishikawa; Hiroki Teraoku; Masato Yoshikawa; Jun Higashijima; Chie Takasu; Mitsuo Shimada
Journal:  In Vivo       Date:  2017 May-Jun       Impact factor: 2.155

4.  IL-8 and eNOS polymorphisms predict bevacizumab-based first line treatment outcomes in RAS mutant metastatic colorectal cancer patients.

Authors:  Mariantonietta Di Salvatore; Filippo Pietrantonio; Armando Orlandi; Marzia Del Re; Rosa Berenato; Ernesto Rossi; Marta Caporale; Donatella Guarino; Antonia Martinetti; Michele Basso; Roberta Mennitto; Concetta Santonocito; Alessia Mennitto; Giovanni Schinzari; Ilaria Bossi; Ettore Capoluongo; Romano Danesi; Filippo de Braud; Carlo Barone
Journal:  Oncotarget       Date:  2017-03-07

5.  Bevacizumab-associated intestinal perforation and perioperative complications in patients receiving bevacizumab.

Authors:  Toshiaki Yoshimoto; Kozo Yoshikawa; Jun Higashijima; Tomohiko Miyatani; Takuya Tokunaga; Masaaki Nishi; Chie Takasu; Hideya Kashihara; Yukako Takehara; Mitsuo Shimada
Journal:  Ann Gastroenterol Surg       Date:  2020-02-12

6.  Blockade of the chemokine receptor, CCR5, reduces the growth of orthotopically injected colon cancer cells via limiting cancer-associated fibroblast accumulation.

Authors:  Yamato Tanabe; Soichiro Sasaki; Naofumi Mukaida; Tomohisa Baba
Journal:  Oncotarget       Date:  2016-07-26
  6 in total

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