Literature DB >> 10436812

Current chemotherapeutic possibilities in pancreaticobiliary cancer.

J M van Riel1, C J van Groeningen, H M Pinedo, G Giaccone.   

Abstract

At time of presentation the majority of patients with pancreaticobiliary cancer have locally advanced or metastatic disease which makes them unamenable for curative surgery. In these patients chemotherapy is an option which has gained more support over the past few years. Special problems faced in chemotherapeutic treatment are the patient's poor condition and the difficulties faced in evaluating response. 5-FU has been the only drug with some efficacy for a long time, but more recently gemcitabine appeared to be more efficient. In locally advanced pancreatic cancer the combination of chemotherapy with radiotherapy has not gained much support. However, studies are implicating better local control with combined treatment and recurrences appear more often at distant sides. In some cases irresectable tumors became resectable. Because of the poor survival after surgery with curative intent, adjuvant and neoadjuvant therapy are becoming important issues. Although studies of adjuvant therapy suggest benefit, research is seriously hampered by poor patient accrual due to the morbidity of pancreaticoduodenectomy. Neoadjuvant treatment may overcome this problem. Until now there has been only modest improvement in the treatment of pancreatic cancer. Hopefully, new treatment modalities such as immunotherapy, gene therapy and antiangiogenic therapy will alter this dismal picture. In biliary cancer the role of chemotherapy is less well defined, since only few studies with low patients numbers have been performed.

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Year:  1999        PMID: 10436812

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  5 in total

1.  Epigenetic regulation affects N-myc downstream-regulated gene 1 expression indirectly in pancreatic cancer cells.

Authors:  Eliane Angst; David W Dawson; Anne Nguyen; Jenny Park; Vay L W Go; Howard A Reber; Oscar Joe Hines; Guido Eibl
Journal:  Pancreas       Date:  2010-07       Impact factor: 3.327

2.  pERK1/2 silencing sensitizes pancreatic cancer BXPC-3 cell to gemcitabine-induced apoptosis via regulating Bax and Bcl-2 expression.

Authors:  Min Wang; Xingjiao Lu; Xueguang Dong; Fengyun Hao; Zimin Liu; Guangzhen Ni; Dong Chen
Journal:  World J Surg Oncol       Date:  2015-02-21       Impact factor: 2.754

3.  Phase II study of S-1 in patients with advanced biliary tract cancer.

Authors:  H Ueno; T Okusaka; M Ikeda; Y Takezako; C Morizane
Journal:  Br J Cancer       Date:  2004-11-15       Impact factor: 7.640

4.  Weekly gemcitabine plus Epirubicin as effective chemotherapy for advanced pancreatic cancer: a multicenter phase II study.

Authors:  B Neri; G Cini; L Doni; C Fulignati; M Turrini; D Pantalone; E Mini; C De Luca Cardillo; L M Fioretto; A S Ribecco; R Moretti; M Scatizzi; G Zocchi; A Quattrone
Journal:  Br J Cancer       Date:  2002-08-27       Impact factor: 7.640

5.  Retinoids cause apoptosis in pancreatic cancer cells via activation of RAR-gamma and altered expression of Bcl-2/Bax.

Authors:  F Pettersson; A G Dalgleish; R P Bissonnette; K W Colston
Journal:  Br J Cancer       Date:  2002-08-27       Impact factor: 7.640

  5 in total

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