Tyrosine kinase inhibitors in osteosarcoma: Adapting treatment strategiesa

被引:11
作者
Assi, Ahmad [1 ]
Farhat, Mohamad [1 ]
Hachem, Maria Catherine Rita [1 ]
Zalaquett, Ziad [1 ]
Aoun, Marven [2 ]
Daher, Mohammad [2 ,3 ]
Sebaaly, Amer [2 ]
Kourie, Hampig-Raphael [1 ]
机构
[1] Hotel Dieu France, Hematol Oncol Dept, Beirut, Lebanon
[2] Hotel Dieu France, Orthoped Dept, Beirut, Lebanon
[3] Brown Univ, Orthoped Dept, Providence, RI USA
关键词
Tyrosine kinase inhibitors; Osteosarcoma; Management; Cancer; Sarcoma; HIGH-GRADE OSTEOSARCOMA; GROWTH-FACTOR RECEPTOR; C-KIT EXPRESSION; PHASE-II; METASTATIC OSTEOSARCOMA; PROGNOSTIC-SIGNIFICANCE; PROTOONCOGENE PRODUCT; RAF/MEK/ERK PATHWAY; SIGNAL-TRANSDUCTION; IMATINIB MESYLATE;
D O I
10.1016/j.jbo.2023.100511
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma (OS) is an aggressive primary bone malignancy that metastasizes rapidly. The standard of care has changed little over the previous four decades, and survival rates have plateaued. In this context, tyrosine kinase inhibitors (TKIs) emerge as potential treatments. A literature search was conducted to collect data related to receptor tyrosine kinase genetic alterations and expression in OS specimens. Gene amplification and protein expression of these receptors were linked to prognosis and tumor behavior. Relevant TKIs were evaluated as monotherapies and as parts of combination therapies. Certain TKIs, such as apatinib, regorafenib, and cabozantinib, present a potential therapeutic avenue for OS patients, especially when combined with chemotherapy. Producing long-lasting responses and enhancing quality of life remain key goals in OS treatment. To this effect, optimizing the use of TKIs by identifying biomarkers predictive of response and assessing promising TKIs in larger-scale trials to validate the efficacy and safety outcomes relative to these drugs reported in phase II clinical trials. To this effect, it is necessary to identify biomarkers predictive of response to TKIs in larger-scale trials and to validate the efficacy and safety of these drugs reported in phase II clinical trials.
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页数:12
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共 127 条
[41]   An EGF receptor/Ral-GTPase signaling cascade regulates c-Src activity and substrate specificity [J].
Goi, T ;
Shipitsin, M ;
Lu, ZM ;
Foster, DA ;
Klinz, SG ;
Feig, LA .
EMBO JOURNAL, 2000, 19 (04) :623-630
[42]   A phase II trial of sorafenib in relapsed and unresectable high-grade osteosarcoma after failure of standard multimodal therapy: an Italian Sarcoma Group study [J].
Grignani, G. ;
Palmerini, E. ;
Dileo, P. ;
Asaftei, S. D. ;
D'Ambrosio, L. ;
Pignochino, Y. ;
Mercuri, M. ;
Picci, P. ;
Fagioli, F. ;
Casali, P. G. ;
Ferrari, S. ;
Aglietta, M. .
ANNALS OF ONCOLOGY, 2012, 23 (02) :508-516
[43]   Sorafenib and everolimus for patients with unresectable high-grade osteosarcoma progressing after standard treatment: a non-randomised phase 2 clinical trial [J].
Grignani, Giovanni ;
Palmerini, Emanuela ;
Ferraresi, Virginia ;
D'Ambrosio, Lorenzo ;
Bertulli, Rossella ;
Asaftei, Sebastian Dorin ;
Tamburini, Angela ;
Pignochino, Ymera ;
Sangiolo, Dario ;
Marchesi, Emanuela ;
Capozzi, Federica ;
Biagini, Roberto ;
Gambarotti, Marco ;
Fagioli, Franca ;
Casali, Paolo Giovanni ;
Picci, Piero ;
Ferrari, Stefano ;
Aglietta, Massimo .
LANCET ONCOLOGY, 2015, 16 (01) :98-107
[44]   The novel c-Met inhibitor cabozantinib overcomes gemcitabine resistance and stem cell signaling in pancreatic cancer [J].
Hage, C. ;
Rausch, V. ;
Giese, N. ;
Giese, T. ;
Schoensiegel, F. ;
Labsch, S. ;
Nwaeburu, C. ;
Mattern, J. ;
Gladkich, J. ;
Herr, I. .
CELL DEATH & DISEASE, 2013, 4 :e627-e627
[45]   Gas6/Axl mediates tumor cell apoptosis, migration and invasion and predicts the clinical outcome of osteosarcoma. patients [J].
Han, Ju ;
Tian, Rui ;
Yong, Bicheng ;
Luo, Canqiao ;
Tan, Pingxian ;
Shen, Jingnan ;
Peng, Tingsheng .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 435 (03) :493-500
[46]   Hallmarks of Cancer: The Next Generation [J].
Hanahan, Douglas ;
Weinberg, Robert A. .
CELL, 2011, 144 (05) :646-674
[47]   Mechanism of action and in vivo role of platelet-derived growth factor [J].
Heldin, CH ;
Westermark, B .
PHYSIOLOGICAL REVIEWS, 1999, 79 (04) :1283-1316
[48]   The FGFR Landscape in Cancer: Analysis of 4,853 Tumors by Next-Generation Sequencing [J].
Helsten, Teresa ;
Elkin, Sheryl ;
Arthur, Elisa ;
Tomson, Brett N. ;
Carter, Jennifer ;
Kurzrock, Razelle .
CLINICAL CANCER RESEARCH, 2016, 22 (01) :259-267
[49]   N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5-(tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a novel, highly selective, orally available, dual-specific c-Src/Abl kinase inhibitor [J].
Hennequin, Laurent F. ;
Allen, Jack ;
Breed, Jason ;
Curwen, Jon ;
Fennell, Michael ;
Green, Tim P. ;
Brempt, Christine Lambert-van der ;
Morgentin, Remy ;
Norman, Richard A. ;
Olivier, Annie ;
Otterbein, Ludovic ;
Ple, Patrick A. ;
Warin, Nicolas ;
Costello, Gerard .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (22) :6465-6488
[50]   Nonclinical Antiangiogenesis and Antitumor Activities of Axitinib (AG-013736), an Oral, Potent, and Selective Inhibitor of Vascular Endothelial Growth Factor Receptor Tyrosine Kinases 1, 2, 3 [J].
Hu-Lowe, Dana D. ;
Zou, Helen Y. ;
Grazzini, Maren L. ;
Hallin, Max E. ;
Wickman, Grant R. ;
Amundson, Karin ;
Chen, Jeffrey H. ;
Rewolinski, David A. ;
Yamazaki, Shinji ;
Wu, Ellen Y. ;
McTigue, Michele A. ;
Murray, Brion W. ;
Kania, Robert S. ;
O'Connor, Patrick ;
Shalinsky, David R. ;
Bender, Steve L. .
CLINICAL CANCER RESEARCH, 2008, 14 (22) :7272-7283