Literature DB >> 17547518

Erlotinib: success of a molecularly targeted agent for the treatment of advanced pancreatic cancer.

Stephen A Welch1, Malcolm J Moore.   

Abstract

Epidermal growth factor receptor (EGFR) is overexpressed by several solid tumors, including pancreatic cancer, and has become an important target for novel anticancer pharmacotherapy. Erlotinib (Tarceva, OSI-774) is an orally available small-molecule inhibitor of the EGFR tyrosine kinase. The addition of erlotinib to gemcitabine has been shown to prolong survival of patients treated for advanced pancreatic cancer in the National Cancer Institute of Canada PA.3 trial. This survival advantage is small yet noteworthy, in that numerous gemcitabine-containing combinations have failed to show a statistically significant survival advantage over gemcitabine alone. The most frequent toxicities associated with the addition of erlotinib are diarrhea and rash. Erlotinib-induced rash appears to be predictive of outcome. Further clinical studies of erlotinib in the treatment of pancreatic cancer are ongoing.

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Year:  2007        PMID: 17547518     DOI: 10.2217/14796694.3.3.247

Source DB:  PubMed          Journal:  Future Oncol        ISSN: 1479-6694            Impact factor:   3.404


  10 in total

1.  Anti-tumor activity of erlotinib in the BxPC-3 pancreatic cancer cell line.

Authors:  Ying-Ying Lu; Da-Dao Jing; Ming Xu; Kai Wu; Xing-Peng Wang
Journal:  World J Gastroenterol       Date:  2008-09-21       Impact factor: 5.742

2.  IL-24 gene transfer sensitizes melanoma cells to erlotinib through modulation of the Apaf-1 and Akt signaling pathways.

Authors:  Wu-Guo Deng; John Kwon; Suhendan Ekmekcioglu; Nancy J Poindexter; Elizabeth A Grimm
Journal:  Melanoma Res       Date:  2011-02       Impact factor: 3.599

3.  KRAS Mouse Models: Modeling Cancer Harboring KRAS Mutations.

Authors:  Rónán C O'Hagan; Joerg Heyer
Journal:  Genes Cancer       Date:  2011-03

4.  miR-34 - a microRNA replacement therapy is headed to the clinic.

Authors:  Andreas G Bader
Journal:  Front Genet       Date:  2012-07-02       Impact factor: 4.599

5.  Allele-specific expression mediates primary resistance to poly (ADP-ribose) polymerase inhibitor therapy in a case of BRCA1/2 double-germline mutant gastric cancer.

Authors:  Lu Wen; Xiuxiu Li; Junping Shi; Shuo Zhang; Rui Wang; Ming Yao; Jun Guo
Journal:  J Int Med Res       Date:  2019-11-27       Impact factor: 1.671

6.  Human RNase3 immune modulation by catalytic-dependent and independent modes in a macrophage-cell line infection model.

Authors:  RanLei Wei; Guillem Prats-Ejarque; Lu Lu; Maria Goetz; Gang Wang; Marc Torrent; Ester Boix
Journal:  Cell Mol Life Sci       Date:  2020-11-23       Impact factor: 9.261

7.  Overexpression of Circular RNA circ_0013587 Reverses Erlotinib Resistance in Pancreatic Cancer Cells Through Regulating the miR-1227/E-Cadherin Pathway.

Authors:  Huiting Xu; Runzhi Chen; Qian Shen; Dongmei Yang; Hui Peng; Jin Tong; Qiang Fu
Journal:  Front Oncol       Date:  2021-09-06       Impact factor: 6.244

8.  Immunohistochemical analysis of changes in signaling pathway activation downstream of growth factor receptors in pancreatic duct cell carcinogenesis.

Authors:  Nhu-An Pham; Joerg Schwock; Vladimir Iakovlev; Greg Pond; David W Hedley; Ming-Sound Tsao
Journal:  BMC Cancer       Date:  2008-02-06       Impact factor: 4.430

9.  Dependence of Relative Expression of NTR1 and EGFR on Cell Density and Extracellular pH in Human Pancreatic Cancer Cell Lines.

Authors:  Ulrike Olszewski-Hamilton; Gerhard Hamilton
Journal:  Cancers (Basel)       Date:  2011-01-04       Impact factor: 6.639

10.  Combination therapy with low-frequency ultrasound irradiation and radiofrequency ablation as a synergistic treatment for pancreatic cancer.

Authors:  Huiyang Wang; Wenxiu Ding; Hongwei Shi; Haiwei Bao; Yuting Lu; Tian An Jiang
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  10 in total

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