TY - JOUR
T1 - A Multi-institutional Study to Diagnose the Risk of Lymph Node Metastasis Using a CRP Genetic Polymorphism Test Kit in pT1, cN0 Thoracic Esophageal Squamous Cell Carcinoma
AU - Motoyama, Satoru
AU - Hosaka, Miki
AU - Kamei, Takashi
AU - Ueno, Masaki
AU - Watanabe, Masayuki
AU - Ohkura, Yu
AU - Mine, Shinji
AU - Tanabe, Shunsuke
AU - Toyokawa, Takahiro
AU - Wakita, Akiyuki
AU - Nishikawa, Katsunori
AU - Ninomiya, Itasu
AU - Fujita, Kazuma
AU - Kanda, Mie
AU - Hirai, Mitsuharu
AU - Hoshi, Manami
AU - Chiu, Shih Wei
AU - Takata, Munenori
AU - Yamaguchi, Takuhiro
AU - Miura, Masatomo
N1 - Funding Information:
This study was supported by AMED under Grant Number JP 19lm0203079. The Authors would like to express our heartfelt gratitude to our collaborators at 65 facilities in allover Japan (B-37 CRP-SNP Study Group). The Authors would also like thank Prof. Ikeda, Ms. Fujiki, Mr. Sakagami, Ms. Ono, and Ms. Kobayashi (Clinical Research Innovation and Education Center, Tohoku University Hospital, Sendai, Japan), Mr. Kawabe for monitoring (Clinical Research Data Center, Tohoku University Hospital, Sendai, Japan), and Yosuke Sato (Akita University Graduate School of Medicine, Akita, Japan) for their assistance.
Publisher Copyright:
© 2022 International Institute of Anticancer Research. All rights reserved.
PY - 2022/12
Y1 - 2022/12
N2 - Background/Aim: For patients with T1a muscularis mucosae (MM) esophageal squamous cell carcinoma (ESCC) with lymphovascular invasion (LVI) or T1b submucosal (SM) ESCC, endoscopic resection is non-curative, and adjuvant treatment entailing esophagectomy or definitive chemoradiotherapy is necessary. This is because about 30% of these cases have lymph node (LN) metastasis. The purpose of this study was to test the utility of a CRP genetic polymorphism test kit for determining the risk of LN metastasis with the aim of eliminating additional invasive adjuvant therapy. Patients and Methods: This is a retrospective, multi-institutional, observational study. The CRP 1846C>T genetic polymorphisms were identified using a fully automated genotyping system. The primary end points were an 85% negative predictive value (NPV) for diagnosis of LN metastasis in pT1a (MM) and 80% NPV in pT1b (SM1) patients. Results: A total of 742 ESCC (105 pMM, 166 pSM1 and 471 pSM2-3) patients who had received esophagectomy with 2- or 3-field LN dissection at 65 institutions were enrolled. According to this test, patients with the C/C and C/T genotypes were considered to be low risk. The NPVs using this test were 82.8% in pMM and 71.7% in pSM1 patients. Conclusion: CRP 1846C>T genetic polymorphism is not a useful diagnostic indicator for determining the risk of LN metastasis; however, the possibility that CRP gene polymorphisms are involved in the mechanism of lymph node metastasis in solid tumors still remains.
AB - Background/Aim: For patients with T1a muscularis mucosae (MM) esophageal squamous cell carcinoma (ESCC) with lymphovascular invasion (LVI) or T1b submucosal (SM) ESCC, endoscopic resection is non-curative, and adjuvant treatment entailing esophagectomy or definitive chemoradiotherapy is necessary. This is because about 30% of these cases have lymph node (LN) metastasis. The purpose of this study was to test the utility of a CRP genetic polymorphism test kit for determining the risk of LN metastasis with the aim of eliminating additional invasive adjuvant therapy. Patients and Methods: This is a retrospective, multi-institutional, observational study. The CRP 1846C>T genetic polymorphisms were identified using a fully automated genotyping system. The primary end points were an 85% negative predictive value (NPV) for diagnosis of LN metastasis in pT1a (MM) and 80% NPV in pT1b (SM1) patients. Results: A total of 742 ESCC (105 pMM, 166 pSM1 and 471 pSM2-3) patients who had received esophagectomy with 2- or 3-field LN dissection at 65 institutions were enrolled. According to this test, patients with the C/C and C/T genotypes were considered to be low risk. The NPVs using this test were 82.8% in pMM and 71.7% in pSM1 patients. Conclusion: CRP 1846C>T genetic polymorphism is not a useful diagnostic indicator for determining the risk of LN metastasis; however, the possibility that CRP gene polymorphisms are involved in the mechanism of lymph node metastasis in solid tumors still remains.
KW - C-reactive protein
KW - endoscopic resection
KW - Esophageal cancer
KW - genetic polymorphism
KW - lymph node metastasis
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U2 - 10.21873/anticanres.16123
DO - 10.21873/anticanres.16123
M3 - Article
C2 - 36456128
AN - SCOPUS:85143183458
SN - 0250-7005
VL - 42
SP - 6105
EP - 6112
JO - Anticancer research
JF - Anticancer research
IS - 12
ER -