Literature DB >> 24222141

Predicting skin toxicity according to EGFR polymorphisms in patients with colorectal cancer receiving antibody against EGFR.

Rie Saito1, Hideo Suzuki, Takeshi Yamada, Shinji Endo, Toshikazu Moriwaki, Takunori Ueno, Mitsuaki Hirose, Sachiko Hirai, Kenji Yamato, Yuji Mizokami, Ichinosuke Hyodo.   

Abstract

BACKGROUND/AIM: Monoclonal antibodies against epidermal growth factor receptor (EGFR) can extend progression-free survival (PFS) and overall survival (OS) in patients with unresectable colorectal cancer; however, skin toxicity often interferes with therapy continuation. PATIENTS AND METHODS: We analyzed the polymorphisms in EGFR and IgG fragment C receptor (FCGR) genes and determined their associations with clinical outcomes including PFS, OS, and skin toxicity. Five polymorphisms in EGFR and FCGR genes in 32 patients with unresectable colorectal cancer who were treated with antibodies against EGFR were examined.
RESULTS: Patients carrying the C/C genotype of the EGFR D994D polymorphism displayed significantly less skin toxicity than those with other genotypes, although no significant differences in PFS and OS were noted and no significant interactions were detected for other gene polymorphisms.
CONCLUSION: These results suggest that the EGFR D994D polymorphism is a useful biomarker for predicting the severity of skin toxicity in patients receiving antibody against EGFR.

Entities:  

Keywords:  EGFR antibody; EGFR gene polymorphism; colorectal cancer; skin toxicity

Mesh:

Substances:

Year:  2013        PMID: 24222141

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  6 in total

Review 1.  Treatment of colorectal cancer in the elderly.

Authors:  Monica Millan; Sandra Merino; Aleidis Caro; Francesc Feliu; Jordi Escuder; Tani Francesch
Journal:  World J Gastrointest Oncol       Date:  2015-10-15

Review 2.  Skin problems and EGFR-tyrosine kinase inhibitor.

Authors:  Toshiyuki Kozuki
Journal:  Jpn J Clin Oncol       Date:  2016-01-29       Impact factor: 3.019

3.  Polymorphism (rs16917496) at the miR-502 Binding Site of the Lysine Methyltransferase 5A (SET8) and Its Correlation with Colorectal Cancer in Iranians.

Authors:  Meysam Mosallayi; Miganoosh Simonian; Sharifeh Khosravi; Ahmad Reza Salehi; Mahsa Khodadoostan; Vahid Sebghatollahi; Azar Baradaran; Rasoul Salehi
Journal:  Adv Biomed Res       Date:  2017-07-14

4.  Genetic Predictors of Severe Skin Toxicity in Patients with Stage III Colon Cancer Treated with Cetuximab: NCCTG N0147 (Alliance).

Authors:  Julia D Labadie; Xinwei Hua; Tabitha A Harrison; Barbara L Banbury; Jeroen R Huyghe; Wei Sun; Qian Shi; Greg Yothers; Steven R Alberts; Frank A Sinicrope; Richard M Goldberg; Thomas J George; Kathryn L Penney; Amanda I Phipps; Stacey A Cohen; Ulrike Peters; Andrew T Chan; Polly A Newcomb
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2020-11-17       Impact factor: 4.090

5.  FCGR2A, FCGR3A polymorphisms and therapeutic efficacy of anti-EGFR monoclonal antibody in metastatic colorectal cancer.

Authors:  Hou-Qun Ying; Feng Wang; Xiao-Lin Chen; Bang-Shun He; Yu-Qin Pan; Chen Jie; Xian Liu; Wei-Jun Cao; Hong-Xin Peng; Kang Lin; Shu-Kui Wang
Journal:  Oncotarget       Date:  2015-09-29

Review 6.  Clinical Pharmacokinetics and Pharmacodynamics of the Epidermal Growth Factor Receptor Inhibitor Panitumumab in the Treatment of Colorectal Cancer.

Authors:  Sander Ketzer; Kirsten Schimmel; Miriam Koopman; Henk-Jan Guchelaar
Journal:  Clin Pharmacokinet       Date:  2018-04       Impact factor: 6.447

  6 in total

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