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Conference Paper: Discordant RAS status between primary and metastatic colorectal cancer and predicted pattern of metastases

TitleDiscordant RAS status between primary and metastatic colorectal cancer and predicted pattern of metastases
Authors
Issue Date2015
PublisherOxford University Press. The Journal's web site is located at http://annonc.oxfordjournals.org/
Citation
The 2015 Congress of the European Society of Medical Oncology Asia (ESMO Asia Congress 2015), Singapore, 18-21 December 2015. In Annals of Oncology, 2015, v. 26 suppl. 9, p. ix46, abstract no. 150PD How to Cite?
AbstractAIM/BACKGROUND: KRAS and NRAS are predictive biomarkers for efficacy of anti-EGFR therapy. Previous studies showed high KRAS concordance between primary tumors and paired metastases while data on NRAS were lacking. This study aims to examine the concordance of KRAS/ NRAS mutation between paired primary and metastatic colorectal tumors. The correlation between pattern of metastases and RAS status was also examined. METHODS: A total of 230 patients diagnosed with metastatic colorectal cancer in August 2013-December 2014 were included. Inclusion criteria were metastatic colorectal cancer new cases in the above period, both primary and metastatic tumor available for test (biopsy or resection), quality of tumor DNA suitable for RAS test. Microdissections, PCR and Sanger sequencing were performed in codon 12/13/61 to determine KRAS/NRAS mutations. Concordance and Cohen Kappa were calculated using SPSS v20. RESULTS: Sixty-seven patients were studied, 67 primary and 82 paired metastatic tumors were examined, 14 patients had more than 1 metastatic tumor examined. The mean age was 62.7 years old (35-88), 44 were males (65.7%), 23 were females (34.3%). The frequency of KRAS, NRAS mutations, wildtype status in primary tumors were 38.8% (26), 4.5% (3) and 56.7% (38) respectively, while the frequency in metastatic tumors were 41.8% (28), 4.5% (3), 53.7% (36) respectively. 8 discordant RAS cases were found. A concordance of 88.1% (59/67) (kappa = 0.759) of RAS mutation was observed between primary and metastatic tumors while the concordance among metastatic sites in same patient was 100%. Among discordant cases, 3 had wildtype metastases, KRAS mutated primary; 5 had KRAS mutated metastases, wildtype primary. No NRAS mutation were discordant. All of 14 liver metastases-only group were concordant. Six of 9 lung metastases-only group were concordant, 39 of 44 multiple-metastases group were concordant between primary and metastatic RAS mutation. The RAS concordance was statistically different among the 3 groups (p= 0.05). Lung metastases-only was associated with a lower RAS concordance (p= 0.033). CONCLUSIONS: The concordance of RAS mutation between primary and paired metastatic tumors was 88.1%. Lung metastases-only was associated with lower RAS concordance.
DescriptionThis journal suppl. entitled: ESMO Asia Congress, 18-21 December 2015, Singapore
Persistent Identifierhttp://hdl.handle.net/10722/229949
ISSN
2015 Impact Factor: 9.269
2015 SCImago Journal Rankings: 4.362

 

DC FieldValueLanguage
dc.contributor.authorLau, KS-
dc.contributor.authorLam, KO-
dc.contributor.authorChoy, TS-
dc.contributor.authorShek, TWH-
dc.contributor.authorChung, LP-
dc.contributor.authorLeung, TW-
dc.date.accessioned2016-08-23T14:14:16Z-
dc.date.available2016-08-23T14:14:16Z-
dc.date.issued2015-
dc.identifier.citationThe 2015 Congress of the European Society of Medical Oncology Asia (ESMO Asia Congress 2015), Singapore, 18-21 December 2015. In Annals of Oncology, 2015, v. 26 suppl. 9, p. ix46, abstract no. 150PD-
dc.identifier.issn0923-7534-
dc.identifier.urihttp://hdl.handle.net/10722/229949-
dc.descriptionThis journal suppl. entitled: ESMO Asia Congress, 18-21 December 2015, Singapore-
dc.description.abstractAIM/BACKGROUND: KRAS and NRAS are predictive biomarkers for efficacy of anti-EGFR therapy. Previous studies showed high KRAS concordance between primary tumors and paired metastases while data on NRAS were lacking. This study aims to examine the concordance of KRAS/ NRAS mutation between paired primary and metastatic colorectal tumors. The correlation between pattern of metastases and RAS status was also examined. METHODS: A total of 230 patients diagnosed with metastatic colorectal cancer in August 2013-December 2014 were included. Inclusion criteria were metastatic colorectal cancer new cases in the above period, both primary and metastatic tumor available for test (biopsy or resection), quality of tumor DNA suitable for RAS test. Microdissections, PCR and Sanger sequencing were performed in codon 12/13/61 to determine KRAS/NRAS mutations. Concordance and Cohen Kappa were calculated using SPSS v20. RESULTS: Sixty-seven patients were studied, 67 primary and 82 paired metastatic tumors were examined, 14 patients had more than 1 metastatic tumor examined. The mean age was 62.7 years old (35-88), 44 were males (65.7%), 23 were females (34.3%). The frequency of KRAS, NRAS mutations, wildtype status in primary tumors were 38.8% (26), 4.5% (3) and 56.7% (38) respectively, while the frequency in metastatic tumors were 41.8% (28), 4.5% (3), 53.7% (36) respectively. 8 discordant RAS cases were found. A concordance of 88.1% (59/67) (kappa = 0.759) of RAS mutation was observed between primary and metastatic tumors while the concordance among metastatic sites in same patient was 100%. Among discordant cases, 3 had wildtype metastases, KRAS mutated primary; 5 had KRAS mutated metastases, wildtype primary. No NRAS mutation were discordant. All of 14 liver metastases-only group were concordant. Six of 9 lung metastases-only group were concordant, 39 of 44 multiple-metastases group were concordant between primary and metastatic RAS mutation. The RAS concordance was statistically different among the 3 groups (p= 0.05). Lung metastases-only was associated with a lower RAS concordance (p= 0.033). CONCLUSIONS: The concordance of RAS mutation between primary and paired metastatic tumors was 88.1%. Lung metastases-only was associated with lower RAS concordance.-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://annonc.oxfordjournals.org/-
dc.relation.ispartofAnnals of Oncology-
dc.rightsPre-print: Journal Title] ©: [year] [owner as specified on the article] Published by Oxford University Press [on behalf of xxxxxx]. All rights reserved. Pre-print (Once an article is published, preprint notice should be amended to): This is an electronic version of an article published in [include the complete citation information for the final version of the Article as published in the print edition of the Journal.] Post-print: This is a pre-copy-editing, author-produced PDF of an article accepted for publication in [insert journal title] following peer review. The definitive publisher-authenticated version [insert complete citation information here] is available online at: xxxxxxx [insert URL that the author will receive upon publication here].-
dc.titleDiscordant RAS status between primary and metastatic colorectal cancer and predicted pattern of metastases-
dc.typeConference_Paper-
dc.identifier.emailLam, KO: lamkaon@hku.hk-
dc.identifier.emailChoy, TS: choyts@hku.hk-
dc.identifier.emailShek, TWH: whshek@hkucc.hku.hk-
dc.identifier.emailLeung, TW: ltw920@hkucc.hku.hk-
dc.identifier.authorityLam, KO=rp01501-
dc.identifier.doi10.1093/annonc/mdv523.11-
dc.identifier.hkuros260821-
dc.identifier.volume26-
dc.identifier.issuesuppl. 9-
dc.identifier.spageix46, abstract no. 150PD-
dc.identifier.epageix46, abstract no. 150PD-
dc.publisher.placeUnited Kingdom-

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