High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population.

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High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population. / Al-Kuraya, Khawla; Siraj, Abdul K; Bavi, Prashant; Al-Jommah, Naif; Ezzat, Adnan; Sheikh, Salwa; Amr, Samir; Al-Dayel, Fouad; Simon, Ronald; Guido, Sauter.

In: HUM PATHOL, Vol. 37, No. 4, 4, 2006, p. 453-457.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Al-Kuraya, K, Siraj, AK, Bavi, P, Al-Jommah, N, Ezzat, A, Sheikh, S, Amr, S, Al-Dayel, F, Simon, R & Guido, S 2006, 'High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population.', HUM PATHOL, vol. 37, no. 4, 4, pp. 453-457. <http://www.ncbi.nlm.nih.gov/pubmed/16564920?dopt=Citation>

APA

Al-Kuraya, K., Siraj, A. K., Bavi, P., Al-Jommah, N., Ezzat, A., Sheikh, S., Amr, S., Al-Dayel, F., Simon, R., & Guido, S. (2006). High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population. HUM PATHOL, 37(4), 453-457. [4]. http://www.ncbi.nlm.nih.gov/pubmed/16564920?dopt=Citation

Vancouver

Al-Kuraya K, Siraj AK, Bavi P, Al-Jommah N, Ezzat A, Sheikh S et al. High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population. HUM PATHOL. 2006;37(4):453-457. 4.

Bibtex

@article{7de1452d81854bfb975b16238090bbca,
title = "High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population.",
abstract = "Epidermal growth factor receptor (EGFR) exon 18-21 mutations were shown to be highly predictive of response to gefitinib (Iressa) therapy in lung cancer. Studies on Western and Japanese lung cancers have indicated substantial differences in the EGFR mutation frequency between these populations. To investigate the prevalence of EGFR in another distinct ethnic group, EGFR alterations were studied in 47 consecutive non small cell lung cancers from Saudi Arabia by immunohistochemistry, fluorescence in situ hybridization, and DNA sequencing. Detectable EGFR expression was seen in 69.8% of 43 interpretable cancers. Epidermal growth factor receptor amplification, present in 15.3% of 39 analyzable cancers, was strongly associated with high levels of EGFR expression (P = .0047). Only 1 exon 18-21 mutation was seen among 34 lung cancers that could be successfully sequenced. It is concluded that EGFR exon 18-21 mutations are rare in Middle East patients with lung cancer and occur in a similar range as in Western patients. The remarkable high rate of EGFR gene amplifications could potentially facilitate studies on the predictive role of gene copy number changes for response to anti-EGFR therapies in Middle East patient sets.",
author = "Khawla Al-Kuraya and Siraj, {Abdul K} and Prashant Bavi and Naif Al-Jommah and Adnan Ezzat and Salwa Sheikh and Samir Amr and Fouad Al-Dayel and Ronald Simon and Sauter Guido",
year = "2006",
language = "Deutsch",
volume = "37",
pages = "453--457",
journal = "HUM PATHOL",
issn = "0046-8177",
publisher = "W.B. Saunders Ltd",
number = "4",

}

RIS

TY - JOUR

T1 - High epidermal growth factor receptor amplification rate but low mutation frequency in Middle East lung cancer population.

AU - Al-Kuraya, Khawla

AU - Siraj, Abdul K

AU - Bavi, Prashant

AU - Al-Jommah, Naif

AU - Ezzat, Adnan

AU - Sheikh, Salwa

AU - Amr, Samir

AU - Al-Dayel, Fouad

AU - Simon, Ronald

AU - Guido, Sauter

PY - 2006

Y1 - 2006

N2 - Epidermal growth factor receptor (EGFR) exon 18-21 mutations were shown to be highly predictive of response to gefitinib (Iressa) therapy in lung cancer. Studies on Western and Japanese lung cancers have indicated substantial differences in the EGFR mutation frequency between these populations. To investigate the prevalence of EGFR in another distinct ethnic group, EGFR alterations were studied in 47 consecutive non small cell lung cancers from Saudi Arabia by immunohistochemistry, fluorescence in situ hybridization, and DNA sequencing. Detectable EGFR expression was seen in 69.8% of 43 interpretable cancers. Epidermal growth factor receptor amplification, present in 15.3% of 39 analyzable cancers, was strongly associated with high levels of EGFR expression (P = .0047). Only 1 exon 18-21 mutation was seen among 34 lung cancers that could be successfully sequenced. It is concluded that EGFR exon 18-21 mutations are rare in Middle East patients with lung cancer and occur in a similar range as in Western patients. The remarkable high rate of EGFR gene amplifications could potentially facilitate studies on the predictive role of gene copy number changes for response to anti-EGFR therapies in Middle East patient sets.

AB - Epidermal growth factor receptor (EGFR) exon 18-21 mutations were shown to be highly predictive of response to gefitinib (Iressa) therapy in lung cancer. Studies on Western and Japanese lung cancers have indicated substantial differences in the EGFR mutation frequency between these populations. To investigate the prevalence of EGFR in another distinct ethnic group, EGFR alterations were studied in 47 consecutive non small cell lung cancers from Saudi Arabia by immunohistochemistry, fluorescence in situ hybridization, and DNA sequencing. Detectable EGFR expression was seen in 69.8% of 43 interpretable cancers. Epidermal growth factor receptor amplification, present in 15.3% of 39 analyzable cancers, was strongly associated with high levels of EGFR expression (P = .0047). Only 1 exon 18-21 mutation was seen among 34 lung cancers that could be successfully sequenced. It is concluded that EGFR exon 18-21 mutations are rare in Middle East patients with lung cancer and occur in a similar range as in Western patients. The remarkable high rate of EGFR gene amplifications could potentially facilitate studies on the predictive role of gene copy number changes for response to anti-EGFR therapies in Middle East patient sets.

M3 - SCORING: Zeitschriftenaufsatz

VL - 37

SP - 453

EP - 457

JO - HUM PATHOL

JF - HUM PATHOL

SN - 0046-8177

IS - 4

M1 - 4

ER -