Literature DB >> 32507561

Current Options for Third-line and Beyond Treatment of Metastatic Colorectal Cancer. Spanish TTD Group Expert Opinion.

Ana Fernández-Montes1, Cristina Grávalos2, Carles Pericay3, Ma José Safont4, Manuel Benavides5, Elena Élez6, Pilar García-Alfonso7, Beatriz García-Paredes8, Alfredo Carrato9, Enrique Aranda10.   

Abstract

Colorectal cancer (CRC) is a public health problem: it is the third most common cancer in men (746,000 new cases/year) and the second in women (614,000 new cases/year), representing the second leading cause of death by cancer worldwide. The survival of patients with metastatic CRC (mCRC) has increased prominently in recent years, reaching a median of 25 to 30 months. A growing number of patients with mCRC are candidates to receive a treatment in third line or beyond, although the optimal drug regimen and sequence are still unknown. In this situation of refractoriness, there are several alternatives: (1) To administer sequentially the 2 oral drugs approved in this indication: trifluridine/tipiracil and regorafenib, which have shown a statistically significant benefit in progression-free survival and overall survival with a different toxicity profile. (2) To administer cetuximab or panitumumab in treatment-naive patients with RAS wild type, which is increasingly rare because these drugs are usually indicated in first- or second-line. (3) To reuse drugs already administered that were discontinued owing to toxicity or progression (oxaliplatin, irinotecan, fluoropyrimidine, antiangiogenics, anti-epidermal growth factor receptor [if RAS wild-type]). High-quality evidence is limited, but this strategy is often used in routine clinical practice in the absence of alternative therapies especially in patients with good performance status. (4) To use specific treatments for very selected populations, such as trastuzumab/lapatinib in mCRC human epidermal growth factor receptor 2-positive, immunotherapy in microsatellite instability, intrahepatic therapies in limited disease or primarily located in the liver, although the main recommendation is to include patients in clinical trials.
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biomarkers; Colorectal neoplasms; Mutations; Refractory; Therapy

Year:  2020        PMID: 32507561     DOI: 10.1016/j.clcc.2020.04.003

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


  4 in total

1.  Previous Use of Anti-Vascular Endothelial Growth Factor Receptor Agents Decreases Efficacy of Fruquintinib in Metastatic Colorectal Cancer Refractory to Standard Therapies.

Authors:  Lei Wang; Huijiao Cao; Chang Jiang; Wenzhuo He; Yafei You; Kunwei Peng; Yanan Jin; Liangping Xia
Journal:  Front Oncol       Date:  2020-11-13       Impact factor: 6.244

2.  Blockade of EIF5A hypusination limits colorectal cancer growth by inhibiting MYC elongation.

Authors:  Sonia Coni; Silvia Maria Serrao; Zuleyha Nihan Yurtsever; Laura Di Magno; Rosa Bordone; Camilla Bertani; Valerio Licursi; Zaira Ianniello; Paola Infante; Marta Moretti; Marialaura Petroni; Francesca Guerrieri; Alessandro Fatica; Alberto Macone; Enrico De Smaele; Lucia Di Marcotullio; Giuseppe Giannini; Marella Maroder; Enzo Agostinelli; Gianluca Canettieri
Journal:  Cell Death Dis       Date:  2020-12-10       Impact factor: 8.469

3.  Comparison of Colorectal Cancer Stem Cells and Oxaliplatin-Resistant Cells Unveils Functional Similarities.

Authors:  Vanessa Rodríguez-Fanjul; Rosa Guerrero-López; Beatriz Fernández-Varas; Rosario Perona; Ana Sastre-Perona; Leandro Sastre
Journal:  Cells       Date:  2022-02-01       Impact factor: 6.600

4.  The Screening and COnsensus Based on Practices and Evidence (SCOPE) Program Results of a Survey on Daily Practice Patterns for Patients with Metastatic Colorectal Cancer-A Swiss Perspective in the Context of an International Viewpoint.

Authors:  Alexander R Siebenhüner; Giorgia Lo Presti; Daniel Helbling; Petr Szturz; Christoforos Astaras; Yannick Buccella; Sara De Dosso
Journal:  Curr Oncol       Date:  2022-08-06       Impact factor: 3.109

  4 in total

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