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Survival paradox between stage IIB/C (T4N0) and stage IIIA (T1-2N1) colon cancer.

作者信息

Kim Min Jung, Jeong Seung-Yong, Choi Sang-Ji, Ryoo Seung-Bum, Park Ji Won, Park Kyu Joo, Oh Jae Hwan, Kang Sung-Bum, Park Hyoung-Chul, Heo Seung Chul, Park Jae-Gahb

机构信息

Center for Colorectal Cancer, National Cancer Center, Goyang, Korea.

出版信息

Ann Surg Oncol. 2015 Feb;22(2):505-12. doi: 10.1245/s10434-014-3982-1. Epub 2014 Aug 22.


DOI:10.1245/s10434-014-3982-1
PMID:25145501
Abstract

BACKGROUND: The survival paradox between stage IIB/C (T4N0) and stage IIIA (T1-2N1) colon cancer remains in the 7th edition of the American Joint Committee on Cancer staging system. This multicenter study aimed to compare the oncologic outcomes of T4N0 and T1-2N1 colon cancers and to investigate the presumptive prognostic factors that might influence the survival paradox. METHODS: Patients who underwent curative surgery for pT4N0 (n = 224) and pT1-2N1 (n = 135) primary colon cancer between January 1999 and December 2010 at five tertiary referral cancer centers were included for analysis. The clinicopathologic, treatment-related factors, and oncologic outcomes in terms of the 5-year overall survival (5-OS) and 5-year disease-free survival (5-DFS) were compared. RESULTS: The T4N0 group had significantly worse 5-OS and 5-DFS rates than the T1-2N1 group (5-OS: 84.0 vs. 92.3 %, p = 0.012; 5-DFS: 73.6 vs. 88.0 %, p = 0.001). T4N0 cancers more frequently showed elevated preoperative carcinoembryonic antigen, lower grade of differentiation, larger tumor size, and higher proportions of perineural invasion, microsatellite instability, obstruction, and perforation than T1-2N1 cancers. Peritoneal seeding and liver metastasis were the predominant recurrence pattern in the T4N0 and T1-2N1 groups, respectively (p = 0.042). The T4N0 group showed inferior survival to the T1-2N1 group in postoperative adjuvant chemotherapy (5-OS: 87.1 vs. 93.2 %, p = 0.045; 5-DFS: 76.1 vs. 89.0 %, p = 0.001). CONCLUSIONS: T4N0 colon cancer had significantly worse oncologic outcomes than T1-2N1 cancer regardless of adjuvant chemotherapy. The survival paradox may result from the biologic aggressiveness of T4N0 colon carcinomas.

摘要

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引用本文的文献

[1]
Prognostic impact and clinical management of pT4N0 colon cancer: data from a large, multicenter, international, real-world dataset.

ESMO Open. 2025-7-15

[2]
Combining Preoperative and Postoperative Prognostic Nutritional Index as an Improved Prognostic Factor for Overall Survival in Patients with Colorectal Cancer.

J Inflamm Res. 2025-7-8

[3]
Evaluation of prognostic models to improve prediction of metastasis in patients following potentially curative treatment for primary colorectal cancer: the PROSPECT trial.

Health Technol Assess. 2025-4

[4]
Determining the optimal number of examined lymph nodes for prognosis in colon cancer: a population-based study stratified by tumor location and T stage.

J Gastrointest Oncol. 2025-2-28

[5]
Patients with T4N0 and T1‑3N1 colon cancer and a high preoperative carcinoembryonic antigen level benefit from adjuvant chemotherapy with oxaliplatin for 6 months.

Oncol Lett. 2024-10-18

[6]
Staging Paradox and recurrence pattern among stage IIB, IIC, and IIIA Colon cancers: a retrospective cohort study.

Int J Colorectal Dis. 2024-10-14

[7]
Revisiting the survival paradox between stage IIB/C and IIIA colon cancer.

Sci Rep. 2024-9-27

[8]
Developing survival prediction models in colorectal cancer using epigenome-wide DNA methylation data from whole blood.

NPJ Precis Oncol. 2024-9-6

[9]
Multivariable prognostic modelling to improve prediction of colorectal cancer recurrence: the PROSPeCT trial.

Eur Radiol. 2024-11

[10]
Predicting 5-year recurrence risk in colorectal cancer: development and validation of a histology-based deep learning approach.

Br J Cancer. 2024-4

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