Oxaliplatin in the treatment of colorectal cancer

被引:23
作者
Kim, George P. [1 ]
Erlichman, Charles [1 ]
机构
[1] Mayo Clin, Jacksonville, FL 32082 USA
关键词
action potential; antibody; antineoplastic agent; camptothecin; colorectal neoplasm; DNA repair; fluorouracil; glutathione S-transferase; hepatic veno-occlusive disease; monoclonal; nerve fiber; organoplatinum compound; polymorphism; survival analysis; NUCLEOTIDE EXCISION-REPAIR; HEPATIC SINUSOIDAL OBSTRUCTION; CONTINUOUS VENOUS INFUSION; DNA MISMATCH REPAIR; PHASE-II TRIAL; PLATINUM COMPLEXES; COLON-CANCER; CELL-LINES; FLUOROURACIL-LEUCOVORIN; THERAPEUTIC OPTION;
D O I
10.1517/17425255.3.2.281
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significant advances in the treatment of colorectal cancer have been observed over the past several years. With the introduction of oxaliplatin combined with infusional 5-fluorouracil and leucovorin, survival for patients with metastatic colorectal cancer has nearly doubled. The incorporation of biologic agents that target angiogenesis (bevacizumab) and tumor growth pathways (cetuximab, panitumimab) extends survival even further, in addition to increasing response rates in patients with metastatic disease. The benefit of these newer drugs is also being realized in the adjuvant setting, where the addition of oxaliplatin to infusional 5-fluorouracil and leucovorin has led to improvements in 3-year disease-free survival. Future challenges with the use of oxaliplatin include defining strategies to optimize its use while avoiding treatment-limiting neurotoxicity and identification of markers predictive of response.
引用
收藏
页码:281 / 294
页数:14
相关论文
共 117 条
[91]  
SALTZ LB, 2007, GI ASCO, V238
[92]   In vitro formation of DNA adducts by cisplatin, lobaplatin and oxaliplatin in calf thymus DNA in solution and in cultured human cells [J].
Saris, CP ;
vandeVaart, PJM ;
Rietbroek, RC ;
Blommaert, FA .
CARCINOGENESIS, 1996, 17 (12) :2763-2769
[93]   Molecular modeling of the intrastrand guanine-guanine DNA adducts produced by cisplatin and oxaliplatin [J].
Scheeff, ED ;
Briggs, JM ;
Howell, SB .
MOLECULAR PHARMACOLOGY, 1999, 56 (03) :633-643
[94]   Cell signaling by receptor tyrosine kinases [J].
Schlessinger, J .
CELL, 2000, 103 (02) :211-225
[95]   Relationships between hydrophobicity, reactivity, accumulation and peripheral nerve toxicity of a series of platinum drugs [J].
Screnci, D ;
McKeage, MJ ;
Galettis, P ;
Hambley, TW ;
Palmer, BD ;
Baguley, BC .
BRITISH JOURNAL OF CANCER, 2000, 82 (04) :966-972
[96]   Severe hepatic sinusoidal obstruction and oxaliplatin-based chemotherapy in patients with metastatic colorectal cancer:: a real entity? [J].
Sebagh, M ;
Plasse, M ;
Lévi, F ;
Adam, R .
ANNALS OF ONCOLOGY, 2005, 16 (02) :331-331
[97]   ERCC1 and thymidylate synthase mRNA levels predict survival for colorectal cancer patients receiving combination oxaliplatin and fluorouracil chemotherapy [J].
Shirota, Y ;
Stoehlmacher, J ;
Brabender, J ;
Xiang, YP ;
Uetake, H ;
Danenberg, KD ;
Groshen, S ;
Tsao-Wei, DD ;
Danenberg, PV ;
Lenz, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (23) :4298-4304
[98]  
Shord SS, 2002, ANTICANCER RES, V22, P2301
[99]   Reaction after oxaliplatin -: prevention with corticosteroids? [J].
Stahl, M ;
Köster, W ;
Wilke, H .
ANNALS OF ONCOLOGY, 2001, 12 (06) :874-874
[100]  
Stoehlmacher J, 2002, J NATL CANCER I, V94, P936