Pancreatic Cancer: Systemic Combination Therapies for a Heterogeneous Disease

被引:44
作者
Melisi, Davide
Calvetti, Lorenzo
Frizziero, Melissa
Tortora, Giampaolo [1 ]
机构
[1] Univ Verona, Dept Med, I-37134 Verona, Italy
关键词
Pancreatic cancer; combination therapies; drug resistance; FOLFIRINOX; nab-paclitaxel; TGF-beta; hypoxia; PHASE-III TRIAL; EPIDERMAL-GROWTH-FACTOR; NF-KAPPA-B; SINGLE-AGENT GEMCITABINE; FACTOR RECEPTOR EGFR; FACTOR-BETA RECEPTOR; ANTI-VEGF TREATMENT; PLUS GEMCITABINE; NAB-PACLITAXEL; TUMOR HYPOXIA;
D O I
10.2174/1381612820666140826154327
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Pancreatic cancer is the only human malignancy for which patients' survival has not improved substantially during the past 30 years. Despite advances in the comprehension of the molecular mechanisms underlying pancreatic carcinogenesis, current systemic treatments offer only a modest benefit in tumor-related symptoms and survival. Over the past decades, gemcitabine and its combination with other standard cytotoxic agents have been the reference treatments for advanced pancreatic cancer patients. The recent introduction of the three-drug combination regimen FOLFIRINOX or the new taxane nab-paclitaxel represent key advances for a better control of the disease. Novel agents targeting molecular mechanisms involved in cancer development and maintenance are currently under clinical investigation. This review describes the most important findings in the field of systemic combination therapies for the treatment of pancreatic cancer. We discuss the emerging evidences for the clinical activity of combination treatments with standard chemotherapy plus novel agents targeting tumor cell-autonomous and tumor microenvironment signaling pathways. We present some of the most important advances in the comprehension of the molecular mechanisms responsible for the chemoresistance of pancreatic cancer and the emerging therapeutic targets to overcome this resistance.
引用
收藏
页码:6660 / 6669
页数:10
相关论文
共 123 条
[1]
Randomized phase III study of exatecan and gemcitabine compared with gemcitabine alone in untreated advanced pancreatic cancer [J].
Abou-Alfa, Ghassan K. ;
Letourneau, Richard ;
Harker, Graydon ;
Modiano, Manuel ;
Hurwitz, Herbert ;
Tchekmedyian, Nerses Simon ;
Feit, Kevie ;
Ackerman, Judie ;
De Jager, Robert L. ;
Eckhardt, S. Gail ;
O'Reilly, Eileen M. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (27) :4441-4447
[2]
[Anonymous], J CLIN ONCOL S
[3]
EGF Receptor Is Required for KRAS-Induced Pancreatic Tumorigenesis [J].
Ardito, Christine M. ;
Gruener, Barbara M. ;
Takeuchi, Kenneth K. ;
Lubeseder-Martellato, Clara ;
Teichmann, Nicole ;
Mazur, Pawel K. ;
DelGiorno, Kathleen E. ;
Carpenter, Eileen S. ;
Halbrook, Christopher J. ;
Hall, Jason C. ;
Pal, Debjani ;
Briel, Thomas ;
Herner, Alexander ;
Trajkovic-Arsic, Marija ;
Sipos, Bence ;
Liou, Geou-Yarh ;
Storz, Peter ;
Murray, Nicole R. ;
Threadgill, David W. ;
Sibilia, Maria ;
Washington, M. Kay ;
Wilson, Carole L. ;
Schmid, Roland M. ;
Raines, Elaine W. ;
Crawford, Howard C. ;
Siveke, Jens T. .
CANCER CELL, 2012, 22 (03) :304-317
[4]
Inhibition of NF-κB sensitizes human pancreatic carcinoma cells to apoptosis induced by etoposide (VP16) or doxorubicin [J].
Arlt, A ;
Vorndamm, J ;
Breitenbroich, M ;
Fölsch, UR ;
Kalthoff, H ;
Schmidt, WE ;
Schäfer, H .
ONCOGENE, 2001, 20 (07) :859-868
[5]
SPARC: a matricellular regulator of tumorigenesis [J].
Arnold, Shanna A. ;
Brekken, Rolf A. .
JOURNAL OF CELL COMMUNICATION AND SIGNALING, 2009, 3 (3-4) :255-273
[6]
Inflammation meets cancer, with NF-κB as the matchmaker [J].
Ben-Neriah, Yinon ;
Karin, Michael .
NATURE IMMUNOLOGY, 2011, 12 (08) :715-723
[7]
Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[8]
Phase III study of gemcitabine in combination with fluorouracil versus gemcitabine alone in patients with advanced pancreatic carcinoma: Eastern Cooperative Oncology Group Trial E2297 [J].
Berlin, JD ;
Catalano, P ;
Thomas, JP ;
Kugler, JW ;
Haller, DG ;
Benson, AB .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (15) :3270-3275
[9]
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes [J].
Biankin, Andrew V. ;
Waddell, Nicola ;
Kassahn, Karin S. ;
Gingras, Marie-Claude ;
Muthuswamy, Lakshmi B. ;
Johns, Amber L. ;
Miller, David K. ;
Wilson, Peter J. ;
Patch, Ann-Marie ;
Wu, Jianmin ;
Chang, David K. ;
Cowley, Mark J. ;
Gardiner, Brooke B. ;
Song, Sarah ;
Harliwong, Ivon ;
Idrisoglu, Senel ;
Nourse, Craig ;
Nourbakhsh, Ehsan ;
Manning, Suzanne ;
Wani, Shivangi ;
Gongora, Milena ;
Pajic, Marina ;
Scarlett, Christopher J. ;
Gill, Anthony J. ;
Pinho, Andreia V. ;
Rooman, Ilse ;
Anderson, Matthew ;
Holmes, Oliver ;
Leonard, Conrad ;
Taylor, Darrin ;
Wood, Scott ;
Xu, Qinying ;
Nones, Katia ;
Fink, J. Lynn ;
Christ, Angelika ;
Bruxner, Tim ;
Cloonan, Nicole ;
Kolle, Gabriel ;
Newell, Felicity ;
Pinese, Mark ;
Mead, R. Scott ;
Humphris, Jeremy L. ;
Kaplan, Warren ;
Jones, Marc D. ;
Colvin, Emily K. ;
Nagrial, Adnan M. ;
Humphrey, Emily S. ;
Chou, Angela ;
Chin, Venessa T. ;
Chantrill, Lorraine A. .
NATURE, 2012, 491 (7424) :399-405
[10]
Capecitabine plus oxaliplatin (CapOx) versus capecitabine plus gemcitabine (CapGem) versus gemcitabine plus oxaliplatin (mGemOx): final results of a multicenter randomized phase II trial in advanced pancreatic cancer [J].
Boeck, S. ;
Hoehler, T. ;
Seipelt, G. ;
Mahlberg, R. ;
Wein, A. ;
Hochhaus, A. ;
Boeck, H. -P. ;
Schmid, B. ;
Kettner, E. ;
Stauchlo, M. ;
Lordick, F. ;
Ko, Y. ;
Geissler, M. ;
Schoppmeyer, K. ;
Kojouharoff, G. ;
Golf, A. ;
Neugebauer, S. ;
Heinemann, V. .
ANNALS OF ONCOLOGY, 2008, 19 (02) :340-347