Abstract | BACKGROUND: Although there are some new criteria for human epidermal growth factor receptor 2 (HER2) expression with immunohistochemistry/fluorescence in situ hybridisation (IHC/FISH) in gastric cancer, the method is still ambiguous and is somewhat dependent on the subjective qualities of the evaluator. METHODS: We used droplet digital polymerase chain reaction (ddPCR) to evaluate HER2 amplification in formalin-fixed and paraffin-embedded (FFPE) samples and cell-free serum circulating tumour DNA (ctDNA) in 25 patients with gastric cancer. RESULTS: The concordance rate of HER2 amplification examined in FFPE samples with ddPCR and IHC/FISH was 92% (23 out of 25). The concordance rate of FFPE with ctDNA was not high (62.5%); however, patients who were HER2-positive by ctDNA had significantly shorter survival compared with HER2-negative patients. CONCLUSIONS: Our results demonstrated that this ddPCR method was as effective as IHC/FISH and therefore might become a standard method for analysing not only FFPE but also ctDNA.
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Authors | H Kinugasa, K Nouso, T Tanaka, K Miyahara, Y Morimoto, C Dohi, T Matsubara, H Okada, K Yamamoto |
Journal | British journal of cancer
(Br J Cancer)
Vol. 112
Issue 10
Pg. 1652-5
(May 12 2015)
ISSN: 1532-1827 [Electronic] England |
PMID | 25897674
(Publication Type: Journal Article)
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Chemical References |
- DNA
- ERBB2 protein, human
- Receptor, ErbB-2
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Topics |
- Adult
- Aged
- Aged, 80 and over
- DNA
(blood)
- Female
- Humans
- In Situ Hybridization, Fluorescence
(methods)
- Male
- Middle Aged
- Paraffin Embedding
(methods)
- Polymerase Chain Reaction
(methods)
- Receptor, ErbB-2
(genetics)
- Stomach Neoplasms
(blood, enzymology, genetics)
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