Pancreatic cancer - A review of emerging therapies

被引:73
作者
Rosenberg, L
机构
[1] McGill Univ, Montreal Gen Hosp, Ctr Hlth, Pancreat Dis Ctr, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Dept Surg, Montreal, PQ H3A 2T5, Canada
关键词
D O I
10.2165/00003495-200059050-00004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The incidence of adenocarcinoma of the pancreas has risen steadily over the past 4 decades, Since pancreatic cancer is diagnosed at an advanced stage, and because of the lack of effective therapies, the prognosis of such patients is extremely poor, Despite advances in our understanding of the molecular biology of pancreatic cancer, the systemic treatment of this disease remains unsatisfactory. Conventional chemotherapy has not produced dramatic improvements in response rates or patient survival, New treatment strategies are clearly needed, This paper reviews emerging therapies for pancreatic carcinoma, A more profound understanding of the molecular biology of cell growth and proliferation, as well as of neoplastic cell transformation, has led to advances in several areas, including the use of somatostatin analogues and antiandrogens as adjuvant therapy; inhibition of tumour growth and metastasis by inhibitors of matrix metalloproteinases and angiogenesis, and by small molecules such as retinoids, which interfere with progression through the cell cycle; immunotherapy with monoclonal antibodies; disruption of intracellular signal transduction with farnesyltransferase inhibitors; and finally gene therapy with specifically designed vaccines.
引用
收藏
页码:1071 / 1089
页数:19
相关论文
共 200 条
[1]   A PHASE-I CLINICAL, PLASMA, AND CELLULAR PHARMACOLOGY STUDY OF GEMCITABINE [J].
ABBRUZZESE, JL ;
GRUNEWALD, R ;
WEEKS, EA ;
GRAVEL, D ;
ADAMS, T ;
NOWAK, B ;
MINEISHI, S ;
TARASSOFF, P ;
SATTERLEE, W ;
RABER, MN ;
PLUNKETT, W .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (03) :491-498
[2]  
ABBRUZZESE JL, 1989, CANCER RES, V49, P4057
[3]  
ABRUZZESE JL, 1992, J BIOL RESP MODIF, V9, P522
[4]  
ABRUZZESE JL, 1997, 33 ANN M, P65
[5]   TUMORS UNDERGOING REJECTION INDUCED BY MONOCLONAL-ANTIBODIES OF THE IGG2A ISOTYPE CONTAIN INCREASED NUMBERS OF MACROPHAGES ACTIVATED FOR A DISTINCTIVE FORM OF ANTIBODY-DEPENDENT CYTOLYSIS [J].
ADAMS, DO ;
HALL, T ;
STEPLEWSKI, Z ;
KOPROWSKI, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (11) :3506-3510
[6]  
*AM CANC SOC, 1991, CANC FACTS FIG 1991
[7]   A CONTROLLED TRIAL OF COMBINATION CHEMOTHERAPY WITH 5-FU AND BCNU IN PANCREATIC-CANCER [J].
ANDERSEN, JR ;
FRIISMOLLER, A ;
HANCKE, S ;
RODER, O ;
STEEN, J ;
BADEN, H .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1981, 16 (08) :973-975
[8]  
ANDRENSANDBERG A, 1982, DIGESTION, V25, P12
[9]   GASTROENTEROPANCREATIC ENDOCRINE TUMORS - EFFECT OF SANDOSTATIN(R) ON TUMOR-GROWTH [J].
ARNOLD, R ;
BENNING, R ;
NEUHAUS, C ;
ROLWAGE, M ;
TRAUTMANN, ME .
DIGESTION, 1993, 54 :72-75
[10]   MOLECULAR-BIOLOGY OF SOMATOSTATIN RECEPTORS [J].
BELL, GI ;
REISINE, T .
TRENDS IN NEUROSCIENCES, 1993, 16 (01) :34-38