What could Nintedanib (BIBF 1120), a triple inhibitor of VEGFR, PDGFR, and FGFR, add to the current treatment options for patients with metastatic colorectal cancer?

被引:32
作者
Capdevila, Jaume [1 ]
Carrato, Alfredo [2 ]
Tabemero, Josep [1 ]
Grande, Enrique [2 ]
机构
[1] Hosp Valle De Hebron, Dept Med Oncol, Barcelona 08035, Spain
[2] Hosp Ramon & Cajal, Dept Med Oncol, Madrid, Spain
关键词
Nintedanib; VEGFR; Angiogenesis; Metastatic colorectal cancer; ENDOTHELIAL GROWTH-FACTOR; TYROSINE KINASE INHIBITOR; OXALIPLATIN-BASED CHEMOTHERAPY; PHASE-II TRIAL; CETUXIMAB PLUS IRINOTECAN; FACTOR-A EXPRESSION; FACTOR RECEPTOR; 1ST-LINE TREATMENT; MICROVESSEL DENSITY; PATIENTS PTS;
D O I
10.1016/j.critrevonc.2014.05.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increasing knowledge of the pro-angiogenic processes involved in the progression of metastatic colorectal cancer (mCRC) has resulted in the clinical development of several anti-angiogenic agents, with bevacizumab currently being the only approved agent for mCRC. Nintedanib (BIBF 1120) has been shown to block the vascular endothelial growth factor receptor (VEGFR), the platelet-derived growth factor receptor (PDGFR), and the fibroblast growth factor receptor (FGFR). By targeting FGFR signaling, nintedanib may overcome resistance to previous anti-VEGF treatments, and may represent a better approach in patients with high basal levels of circulating FGFs. In this article, the angiogenic mechanisms implicated in mCRC are reviewed (focusing on the signaling pathways activated by VEGFR, PDGFR, and FGFR), along with the clinical data for nintedanib in the context of other anti-angiogenic tyrosine kinase inhibitors under clinical development for mCRC. Biomarkers that could predict response to nintedanib are also discussed. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:83 / 106
页数:24
相关论文
共 156 条
[1]  
[Anonymous], ASCO M S
[2]  
[Anonymous], 2011, STUDY FOLFIRI CHEMOT
[3]  
Appelmann I, 2010, RECENT RESULTS CANC, V180, P51, DOI 10.1007/978-3-540-78281-0_5
[4]   Shed alcam as a biomarker for urogenital cancers [J].
Arnold, Shanna ;
Jones-Paris, Celestial ;
Hansen, Amanda Georgia ;
Fadare, Oluwole ;
Clark, Peter ;
Zijlstra, Andries .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (30)
[5]   SYNERGISTIC EFFECT OF VASCULAR ENDOTHELIAL GROWTH-FACTOR AND BASIC FIBROBLAST GROWTH-FACTOR ON ANGIOGENESIS IN-VIVO [J].
ASAHARA, T ;
BAUTERS, C ;
ZHENG, LP ;
TAKESHITA, S ;
BUNTING, S ;
FERRARA, N ;
SYMES, JF ;
ISNER, JM .
CIRCULATION, 1995, 92 (09) :365-371
[6]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[7]   The angiogenic switch in carcinogenesis [J].
Baeriswyl, Vanessa ;
Christofori, Gerhard .
SEMINARS IN CANCER BIOLOGY, 2009, 19 (05) :329-337
[8]   Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[9]   The multifaceted circulating endothelial cell in cancer: towards marker and target identification [J].
Bertolini, Francesco ;
Shaked, Yuval ;
Mancuso, Patrizia ;
Kerbel, Robert S. .
NATURE REVIEWS CANCER, 2006, 6 (11) :833-845
[10]   Insight into the physiological functions of PDGF through genetic studies in mice [J].
Betsholtz, C .
CYTOKINE & GROWTH FACTOR REVIEWS, 2004, 15 (04) :215-228