EGFR Protein Expression of KRAS Wild-Type Colorectal Cancer: Predictive Value of the Sidedness for Efficacy of Anti-EGFR Therapy.


Journal

Pathology oncology research : POR
ISSN: 1532-2807
Titre abrégé: Pathol Oncol Res
Pays: Switzerland
ID NLM: 9706087

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 27 11 2018
accepted: 21 12 2018
pubmed: 7 1 2019
medline: 2 4 2021
entrez: 7 1 2019
Statut: ppublish

Résumé

Right- and left-sided colorectal cancers (RSCRC and LSCRC, respectively) are different developmentally, genetically and prognostically. Clinical data also indicate that they respond differently to anti-EGFR therapies. The role of EGFR protein expression in KRAS wild type colorectal cancer is also controversial. Here we have used a cohort of anti-EGFR antibody treated KRAS-wild type colorectal cancer patients (n = 97) to analyse the prognostic role of EGFR protein expression in relation to sidedness. In our cohort EGFR copy number, determined by FISH, was not associated with the level of EGFR protein, assessed by immunohistochemistry and measured by H-scoring. There was a significantly higher EGFR H-score detected in RSCRC as compared to LSCRC in primary tumors (p = 0.04). Furthermore, in a proportion of cases (n = 31) metastatic tissues were also available and their analysis also found a significantly higher EGFR H-score in metastases of RSCRC compared to LSCRC (p = 0.018). Kaplan Meyer survival analysis demonstrated that anti-EGFR antibody therapies were more effective in case of LSCRC compared to RSCRC. Although in case of progression-free survival data just indicated a trend (p = 0.065), in case of overall survival the difference was significant favouring LSCRC (p = 0.047). These data demonstrated for the first time that the EGFR protein expression is significantly higher in KRAS wild type RSLCL as compared to LSCRC. Meanwhile it is somewhat unexpected that the lower EGFR protein expression was found to be associated with better efficacy of anti-EGFR antibody therapies of colorectal cancer, the finding of which must be further validated.

Identifiants

pubmed: 30612313
doi: 10.1007/s12253-018-00572-2
pii: 10.1007/s12253-018-00572-2
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
KRAS protein, human 0
Panitumumab 6A901E312A
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Proto-Oncogene Proteins p21(ras) EC 3.6.5.2
Cetuximab PQX0D8J21J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1429-1434

Subventions

Organisme : Nemzeti Kutat?si, Fejleszt?si ?s Innov?ci?s Hivatal
ID : K116151

Auteurs

A Uhlyarik (A)

Department of Oncology, Medical Center, Hungarian Defence Forces, Budapest, Hungary.

V Piurko (V)

2nd Department of Pathology, Semmelweis University, 93 Üllöi str, Budapest, 1091, Hungary.

L Vizkeleti (L)

2nd Department of Pathology, Semmelweis University, 93 Üllöi str, Budapest, 1091, Hungary.

Zs Pápai (Z)

Department of Oncology, Medical Center, Hungarian Defence Forces, Budapest, Hungary.

E Rásó (E)

2nd Department of Pathology, Semmelweis University, 93 Üllöi str, Budapest, 1091, Hungary.

E Lahm (E)

Department of Oncology, Medical Center, Hungarian Defence Forces, Budapest, Hungary.

E Kiss (E)

Department of Oncology, Medical Center, Hungarian Defence Forces, Budapest, Hungary.

M Sikter (M)

Department of Oncology, Medical Center, Hungarian Defence Forces, Budapest, Hungary.

J Vachaja (J)

Department of Oncology, Medical Center, Hungarian Defence Forces, Budapest, Hungary.

I Kenessey (I)

2nd Department of Pathology, Semmelweis University, 93 Üllöi str, Budapest, 1091, Hungary.

József Tímár (J)

2nd Department of Pathology, Semmelweis University, 93 Üllöi str, Budapest, 1091, Hungary. jtimar@gmail.com.

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Classifications MeSH