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Analysis of the Characteristics of Coexisting Lesions in Colorectal Cancer Patients in an International Study: A Subgroup Analysis of the ATLAS Trial.
Yoshida, Naohisa; Suzuki, Sho; Inoue, Ken; Aniwan, Satimai; Chiu, Han-Mo; Laohavichitra, Kannikar; Chirapongsathorn, Sakkarin; Yamamura, Takeshi; Kuo, Chen-Ya; Ang, Tiing Leong; Takezawa, Takahito; Rerknimitr, Rungsun; Ishikawa, Hideki.
Afiliación
  • Yoshida N; Department of Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, Japan, naohisa@koto.kpu-m.ac.jp.
  • Suzuki S; Department of Gastroenterology and Hepatology, International University of Health and Welfare, School of Medicine, Chiba, Japan.
  • Inoue K; Department of Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Aniwan S; Center of Excellence in Endoscopy for Gastrointestinal Oncology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Chiu HM; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Laohavichitra K; Rajavithi Digestive Endoscopy Center, Rajavithi Hospital, Bangkok, Thailand.
  • Chirapongsathorn S; Division of Gastroenterology and Hepatology, Department of Medicine, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand.
  • Yamamura T; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kuo CY; Department of Internal Medicine, Fu Jen Catholic University Hospital, New Taipei City, Taiwan.
  • Ang TL; Department of Gastroenterology and Hepatology, Changi General Hospital, SingHealth, Singapore, Singapore.
  • Takezawa T; Division of Gastroenterology, Department of Medicine, Jichi Medical University, Tochigi, Japan.
  • Rerknimitr R; Center of Excellence in Endoscopy for Gastrointestinal Oncology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Ishikawa H; Department of Molecular-Targeting Cancer Prevention, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Digestion ; : 1-11, 2024 Apr 18.
Article en En | MEDLINE | ID: mdl-38631318
ABSTRACT

INTRODUCTION:

We investigated coexisting lesion types in patients with invasive colorectal cancer (CRC) in a multinational study for comprehending the adenoma-carcinoma and serrated pathway about the development of CRC.

METHODS:

We retrospectively reviewed 3,050 patients enrolled in the international randomized controlled trial (ATLAS study) to evaluate the colorectal polyp detection performance of image-enhanced endoscopy in 11 institutions in four Asian countries/regions. In the current study, as a subgroup analysis of the ATLAS study, 92 CRC patients were extracted and compared to 2,958 patients without CRC to examine the effects of age, sex, and coexisting lesion types (high-grade adenoma [HGA], low-grade adenoma with villous component [LGAV], 10 adenomas, adenoma ≥10 mm, sessile serrated lesions [SSLs], and SSLs with dysplasia [SSLD]). Additional analyses of coexisting lesion types were performed according to sex and location of CRC (right- or left-sided).

RESULTS:

A multivariate analysis showed that HGA (odds ratio [95% confidence interval] 4.29 [2.16-8.18]; p < 0.01), LGAV (3.02 [1.16-7.83], p = 0.02), and age (1.04 [1.01-1.06], p = 0.01) were independently associated with CRC. According to sex, the coexisting lesion types significantly associated with CRC were LGAV (5.58 [1.94-16.0], p < 0.01) and HGA (4.46 [1.95-10.20], p < 0.01) in males and HGA (4.82 [1.47-15.80], p < 0.01) in females. Regarding the location of CRC, SSLD (21.9 [1.31-365.0], p = 0.03) was significant for right-sided CRC, and HGA (5.22 [2.39-11.4], p < 0.01) and LGAV (3.46 [1.13-10.6], p = 0.02) were significant for left-sided CRC.

CONCLUSIONS:

The significant coexisting lesions in CRC differed according to sex and location. These findings may contribute to comprehending the pathogenesis of CRC.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Digestion Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Digestion Año: 2024 Tipo del documento: Article
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