• 検索結果がありません。

High cytokeratin 19 fragment/carcinoembryonic antigen ratio is a negative predictor of EGFR T790M mutation in EGFR-mutant NSCLC patients after EGFR-TKI failure<Abstract of dissertation>

N/A
N/A
Protected

Academic year: 2021

シェア "High cytokeratin 19 fragment/carcinoembryonic antigen ratio is a negative predictor of EGFR T790M mutation in EGFR-mutant NSCLC patients after EGFR-TKI failure<Abstract of dissertation>"

Copied!
2
0
0

読み込み中.... (全文を見る)

全文

(1)

Nagoya City University Academic Repository

学 位 の 種 類 博士 (医学) 報 告 番 号 甲第1574号 学 位 記 番 号 第1129号 氏 名 古田 裕美 授 与 年 月 日 平成 29 年 3 月 24 日 学位論文の題名

High cytokeratin 19 fragment/carcinoembryonic antigen ratio is a negative predictor of EGFR T790M mutation in EGFR-mutant NSCLC patients after EGFR-TKI failure

(EGFR-TKI 獲得耐性後の EGFR 変異陽性非小細胞肺癌患者において EGFR T790M 変異の負の予測因子となりうる、高サイトケラチン 19 フラグメント /癌胎児性抗原(CEA)比)

Nagoya Medical Journal (accepted)

論文審査担当者 主査: 中西 良一

(2)

Abstract

The association between tumor markers, carcinoembryonic antigen (CEA) and cytokeratin 19

fragments (CYFRA21-1), and T790M point mutation in exon 20 (T790M) status after the

resistance to epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) remains

unclear. We retrospectively analyzed 126 advanced EGFR-mutant NSCLC patients who were

subsequently re-biopsied to investigate T790M mutation following resistance to initial

EGFR-TKIs. Results: Serum CYFRA21-1 level was significantly associated with T790M

mutation ([<3.5 ng/mL]: 59.7% versus [3.5 ng/mL≦]: 38.8%, P = 0.0217). Moreover, patients

with high CYFRA21-1/CEA (<0.7) ratio had a significantly lower prevalence of T790M

mutation than those with low ratio (≧0.7) [25.4% versus 74.6%, P = 0.007]. Multivariate

analysis showed that high CYFRA21-1/CEA ratio is a negative predictor of T790M mutation

[odds ratio: 0.226 (95% confidence interval: 0.051–0.834), P = 0.025]. In conclusion, igh

参照

関連したドキュメント

Since Ca 2+ /calmodulin-dependent protein kinase II (CaMKII), which is NMDA receptor downstream kinase, is essential for memory and learning acquisition, we developed a protocol

HER2 TKI, to induce regression in patients with adenocarcinoma of the lung and activating EGFR muta- tions : preliminary results of a single-arm phase II clinical trial. J Thorac

01337765 Ib Novartis BEZ235 (PI3K ⁄ mTOR inhibitor) MEK162 At the MTD dose, this combination was assessed in patients with EGFR mutant NSCLC, whom have progressed on EGFR inhibitors

Abbreviations: AR, androgen receptor; BDNF, brain-derived neurotropic factor; DM, diabetes mellitus; DR4, 5, death receptor 4, 5; EGF, epidermal growth factor; GSK3β, glycogen

Expression of erythropoietin (EPO), thrombopoietin (TPO), and stem cells factor (SCF) was examined by RT-PCR analysis in (1) PDGFRa negative fraction, (2) PDGFRa positive fraction,

In our previous study, an in vitro kinase inhibition assay with ICO1686 and CO-1686 showed their high selectivity toward double mutations EGFR L858R/T790M compared with that

PDGFRβ-targeted imaging agents, which are radiolabeled probes using several types of carrier molecules with a high affinity for PDGFRβ, such as PDGF ligand protein [8,9], ap-

In the normal pancreas, moderate to marked basic FGF immuno- reactivity was present in a heterogeneous pattern at the basal aspect of acinar cells, and intense cytoplasmic FGF