Clinicopathological and Molecular Characteristics of Early-Onset Stage III Colon Adenocarcinoma: An Analysis of the ACCENT Database

被引:30
作者
Jin, Zhaohui [1 ]
Dixon, Jesse G. [2 ]
Fiskum, Jack M. [2 ]
Parekh, Hiral D. [3 ]
Sinicrope, Frank A. [1 ]
Yothers, Greg [4 ]
Allegra, Carmen J. [5 ]
Wolmark, Norman [6 ]
Haller, Daniel [7 ]
Schmoll, Hans-Joachim [8 ]
de Gramont, Aimery [9 ]
Kerr, Rachel [10 ]
Taieb, Julien [11 ]
Van Cutsem, Eric [12 ,13 ]
Tweleves, Christopher [14 ,15 ]
O'Connell, Michael [1 ]
Saltz, Leonard B. [1 ]
Sadahiro, Sotaro [16 ]
Blanke, Charles D. [17 ]
Tomita, Naohiro [18 ]
Seitz, Jean-Francois [19 ]
Erlichman, Charles [1 ]
Yoshino, Takayuki [20 ]
Yamanaka, Takeharu [21 ]
Marsoni, Silvia [22 ]
Andre, Thierry [23 ]
Mahipal, Amit [1 ]
Goldberg, Richard M. [24 ,25 ]
George, Thomas J. [26 ]
Shi, Qian [2 ]
机构
[1] Mayo Clin, Dept Oncol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Quantitat Hlth Sci, Rochester, MN 55905 USA
[3] Canc Specialists North Florida, Jacksonville, FL USA
[4] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15261 USA
[5] Univ Florida, Dept Med, Shands Canc Ctr, Gainesville, FL USA
[6] Univ Pittsburgh, Pittsburgh, PA USA
[7] Univ Penn, Abramson Canc Ctr, Perelman Sch Med, Philadelphia, PA 19104 USA
[8] Martin Luther Univ Halle Wittenberg, Univ Clin Halle Saale, Dept Internal Med Hematol Oncol 4, Halle, Germany
[9] Franco British Inst, Dept Med Oncol, Levallois Perret, France
[10] Univ Oxford, Oxford, England
[11] Paris Descartes Univ, Sorbonne Paris Cite, Georges Pompidou European Hosp, Paris, France
[12] Univ Hosp Gasthuisberg Leuven, Digest Oncol, Leuven, Belgium
[13] Katholieke Univ Leuven, Leuven, Belgium
[14] Univ Leeds, Bradford, W Yorkshire, England
[15] Univ Bradford, Tom Connors Canc Res Ctr, St Jamess Inst Oncol, Bradford, W Yorkshire, England
[16] Tokai Univ, Dept Surg, Tokyo, Japan
[17] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[18] Toyonaka City Hosp, Canc Treatment Ctr, Toyonaka, Osaka, Japan
[19] Hop La Timone, Marseille, France
[20] Natl Canc Ctr Hosp East, Dept Gastrointestinal Oncol, Kashiwa, Chiba, Japan
[21] Yokohama City Univ, Dept Biostat, Sch Med, Yokohama, Kanagawa, Japan
[22] FIRC Inst Mol Oncol, Milan, Italy
[23] St Antoine Hosp, AP HP, Med Oncol Dept, Paris, France
[24] West Virginia Univ, Canc Inst, Morgantown, WV 26506 USA
[25] West Virginia Univ, Mary Babb Randolph Canc Ctr, Morgantown, WV 26506 USA
[26] Univ Florida, Hlth Canc Ctr, Gainesville, FL USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2021年 / 113卷 / 12期
关键词
DNA MISMATCH REPAIR; COLORECTAL-CANCER; ADJUVANT THERAPY; SURVIVAL RATES; YOUNG; FLUOROURACIL; OUTCOMES; RISK; OXALIPLATIN; DISPARITIES;
D O I
10.1093/jnci/djab123
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Colon cancer (CC) incidence in young adults (age 20-49 years), termed early-onset CC (EO-CC), is increasing. Methods: Individual patient data on 35 713 subjects with stage III colon cancer from 25 randomized studies in the Adjuvant Colon Cancer ENdpoint database were pooled. The distributions of demographics, clinicopathological features, biomarker status, and outcome data were summarized by age group. Overall survival, disease-free survival, time to recurrence, and survival after recurrence were assessed by Kaplan-Meier curves and Cox models stratified by treatment arms within studies, adjusting for sex, race, body mass index, performance status, disease stage, grade, risk group, number of lymph nodes examined, disease sidedness, and molecular markers. All statistical tests were 2-sided. Results: Using a 5% difference between age groups as the clinically meaningful cutoff, patients with stage III EO-CC had similar sex, race, performance status, risk group, tumor sidedness, and T stage compared with patients with late-onset CC (age 50 years and older). EO-CC patients were less likely to be overweight (30.2% vs 36.2%) and more commonly had 12 or more lymph nodes resected (69.5% vs 58.7%). EO-CC tumors were more frequently mismatch repair deficient (16.4% vs 11.5%) and less likely to have BRAFV600E (5.6% vs 14.0%), suggesting a higher rate of Lynch syndrome in EO-CC. Patients with EO-CC had statistically significantly better overall survival (hazard ratio [HR] 1/4 0.81, 95% confidence interval [CI] 1/4 0.74 to 0.89; P<.001), disease-free survival (HR <1/4> 0.91, 95% CI 1/4 0.84 to 0.98; P 1/4 .01), and survival after recurrence (HR 1/4 0.88, 95% CI 1/4 0.80 to 0.97; P 1/4 .008) in the analysis without molecular markers; however, age at onset of CC lost its prognostic value when outcome was adjusted for molecular markers. Conclusion: Tumor biology was found to be a more important prognostic factor than age of onset among stage III colon cancer patients in the Adjuvant Colon Cancer ENdpoint database.
引用
收藏
页码:1693 / 1704
页数:12
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