Systemic cancer therapy: Evolution over the last 60 years

被引:42
作者
Dy, Grace K. [1 ]
Adjei, Alex A. [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
关键词
signal transduction; cancer chemotherapy; monoclonal antibodies; tyrosine kinase;
D O I
10.1002/cncr.23651
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The 1940s marked the beginning of all era of important discoveries that contributed to modern concepts underlying the current practice of cancer chemotherapy, such as the log kill hypothesis reported by Skipper, the Norton-Simon hypothesis, and the Goldie-Coldman hypothesis. The early success of nitrogen mustards and antifolates in the treatment of hematologic malignancies paved the way for drug discovery platforms, which resulted in the generation of more drugs that nonetheless predominantly are genotoxic. The turn of the new millennium marked a new phase in the evolution of cancer chemotherapy. Scientific progress in the preceding 60 years elucidated the important ideas behind tumor microenvironment and 'targeted' therapy that had their inception in the late 19th century. Breakthroughs in molecular biology have paved the way for the development of novel agents that modulate the dysregulated molecular pathways implicated in carcinogenesis. The key approaches and evidence pertinent to the clinical development of these novel agents are presented in this review.
引用
收藏
页码:1857 / 1887
页数:31
相关论文
共 242 条
[1]   Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia [J].
Abu-Duhier, FM ;
Goodeve, AC ;
Wilson, GA ;
Care, RS ;
Peake, IR ;
Reilly, JT .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (04) :983-988
[2]   FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group [J].
Abu-Duhier, FM ;
Goodeve, AC ;
Wilson, GA ;
Gari, MA ;
Peake, IR ;
Rees, DC ;
Vandenberghe, EA ;
Winship, PR ;
Reilly, JT .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) :190-195
[3]   Experimental and clinical studies on the treatment of cancer by dichlorethylsulphide (mustard gas) [J].
Adair, FE ;
Bagg, HJ .
ANNALS OF SURGERY, 1931, 93 :190-199
[4]   The proteasome: A suitable antineoplastic target [J].
Adams, J .
NATURE REVIEWS CANCER, 2004, 4 (05) :349-360
[5]   Antisense and siRNA as agonists of Toll-like receptors [J].
Agrawal, S ;
Kandimalla, ER .
NATURE BIOTECHNOLOGY, 2004, 22 (12) :1533-1537
[6]  
AIDA S, 1994, RESPIRATION, V61, P161
[7]   The promise of retinoids to fight against cancer [J].
Altucci, L ;
Gronemeyer, H .
NATURE REVIEWS CANCER, 2001, 1 (03) :181-193
[8]  
*AMG INC, 2007, AMG DISC VECT TREATM
[9]  
[Anonymous], 1865, BERL KLINISCHE WOCHE
[10]   Response to imatinib mesylate in patients with chronic myeloproliferative diseases with rearrangements of the platelet-derived growth factor receptor beta [J].
Apperley, JF ;
Gardembas, M ;
Melo, JV ;
Russell-Jones, R ;
Bain, BJ ;
Baxter, J ;
Chase, A ;
Chessells, JM ;
Colombat, M ;
Dearden, CE ;
Dimitrijevic, S ;
Mahon, FX ;
Marin, D ;
Nikolova, Z ;
Olavarria, E ;
Silberman, S ;
Schultheis, B ;
Cross, NCP ;
Goldman, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (07) :481-487