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中华结直肠疾病电子杂志 ›› 2024, Vol. 13 ›› Issue (03) : 236 -241. doi: 10.3877/cma.j.issn.2095-3224.2024.03.009

论著

伴有错配修复缺陷的病理Ⅱ期结直肠癌临床病理特征分析及生存分析
程璞1, 郑朝旭1,()   
  1. 1. 100021 北京,国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院结直肠外科
  • 收稿日期:2024-03-11 出版日期:2024-06-25
  • 通信作者: 郑朝旭
  • 基金资助:
    中国癌症基金会北京希望马拉松专项基金(LC2021A23)

The analysis of clinicopathological characteristics and survival of pathological stage Ⅱ colorectal cancer with mismatch repair deficiency status

Pu Cheng1, Zhaoxu Zheng1,()   

  1. 1. Department of Colorectal Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
  • Received:2024-03-11 Published:2024-06-25
  • Corresponding author: Zhaoxu Zheng
引用本文:

程璞, 郑朝旭. 伴有错配修复缺陷的病理Ⅱ期结直肠癌临床病理特征分析及生存分析[J]. 中华结直肠疾病电子杂志, 2024, 13(03): 236-241.

Pu Cheng, Zhaoxu Zheng. The analysis of clinicopathological characteristics and survival of pathological stage Ⅱ colorectal cancer with mismatch repair deficiency status[J]. Chinese Journal of Colorectal Diseases(Electronic Edition), 2024, 13(03): 236-241.

目的

探究伴有错配修复缺陷(dMMR)的病理Ⅱ期结直肠癌患者临床病理特征及其生存分析。

方法

纳入2011年1月至2017年12月在中国医学科学院肿瘤医院接受手术治疗后经病理免疫组化检查确诊伴有dMMR的病理Ⅱ期结直肠癌患者的临床病理资料。随后进行关于5年总体生存期(OS)和无病生存期(DFS)的单因素及多因素Cox分析,明确影响伴有dMMR的病理Ⅱ期结直肠癌患者生存的相关影响因素。

结果

共纳入70例伴有dMMR的病理Ⅱ期结直肠癌患者,全组患者中40例(57%)为男性、45例(64%)年龄<60岁、64例(91%)患者身体质量指数≥18.5 kg/m2、主要为结肠癌(52例,74%);大多数为癌胚抗原(CEA)(53例,76%)及CA19-9(60例,86%)阴性患者;39例(56%)肿瘤大小>5 cm;腺癌(51例,73%)是占据比例最多的病理类型并且主要为中分化(39例,56%);60例(86%)患者为病理T3期;43例(61%)患者未行辅助化疗以及有44例(63%)患者临床淋巴结分期为cN+期;全组中位病理淋巴结大小为0.70 cm;中位检出淋巴结个数为25.50个。单因素及多因素Cox分析表明肿瘤位置(5年OS:HR:0.097,95%CI:0.019~0.481,P=0.004;5年DFS:HR:0.206,95%CI:0.058~0.733,P=0.015)及临床淋巴结分期(5年OS:HR:0.171,95%CI:0.034~0.852,P=0.031;5年DFS:HR:0.131,95%CI:0.028~0.620,P=0.010)是伴有dMMR的病理Ⅱ期结直肠癌患者5年OS及DFS的独立影响因素。

结论

伴有dMMR的病理Ⅱ期结直肠癌发病年龄较轻并且病期偏早、多位于结肠、肿瘤偏大及患者身体质量指数较高、肿瘤标志物多为阴性并且大多未行术后辅助化疗,除此以外,临床淋巴结分期多为cN+期。生存分析也表明肿瘤位置及临床淋巴结分期是5年OS及DFS的独立影响因素。

Objective

To analyze the clinicopathological characteristics and survival of pathological stage Ⅱ colorectal cancer with mismatch repair deficiency (dMMR) status.

Methods

The pathological stage Ⅱ colorectal cancer with dMMR diagnosed with pathologically immunohistochemistry staining after surgery from January 2011 to December 2017 were enrolled. The clinicopathological characteristics of these patients were statistically analyzed. Subsequently, the univariate and multivariate Cox regression analysis about 5-year overall survival (OS) and disease free survival (DFS) were conducted.

Results

A total of 70 patients with pathological stage Ⅱ CRC with dMMR were included. The majority of the patients were male (40 cases, 57%) and under 60 years old (45 cases, 64%). 64 patients (91%) had a body mass index (BMI) of ≥18.5 kg/m2. Tumors located in the colon accounted for 52 cases (74%). Carcinoembryonic antigen (CEA) negative and CA19-9 negative were observed in 53 cases (76%) and 60 cases (86%), respectively. Tumor size was larger than 5 cm in 39 cases (56%). Adenocarcinoma (51 cases, 73%) was the most common pathological type, predominantly moderately differentiated (39 cases, 56%). Pathological stage T3 was observed in 60 patients (86%). Forty-three patients (61%) did not receive adjuvant chemotherapy, and 44 patients (63%) had clinically positive lymph node stage (cN+ stage). The median size of the examined lymph nodes in the entire group was 0.70 cm. The median number of detected lymph nodes was 25.50. Univariate and multivariate Cox analysis showed that tumor location (5-year OS: HR: 0.097, 95%CI: 0.019~0.481, P=0.004; 5-year DFS: HR: 0.206, 95%CI: 0.058~0.733, P=0.015) and clinical lymph node stage (5-year OS: HR: 0.171, 95%CI: 0.034~0.852, P=0.031; 5-year DFS: HR, 0.131, 95%CI: 0.028~0.620, P=0.010) were independent influencing factors for 5-year OS and DFS of pathological stage Ⅱ colorectal cancer with dMMR.

Conclusion

Pathological stage Ⅱ colorectal cancer with dMMR tend to be younger and have earlier-stage disease. The tumors are more commonly located in the colon, larger in size, and the patients have a higher BMI. Tumor markers are usually negative, and adjuvant chemotherapy is not commonly administered. Additionally, clinical lymph node stage often shows cN+ stage. Survival analysis about 5-year OS and DFS demonstrates that tumor location and clinical lymph node stage are independent influencing factors.

表1 伴有dMMR的病理Ⅱ期结直肠癌患者的临床病理特征[例(%)]
表2 伴有dMMR的病理Ⅱ期结直肠癌患者5年OS的单因素和多因素Cox分析
表3 伴有dMMR的病理Ⅱ期结直肠癌患者5年DFS的单因素和多因素Cox分析
[1]
Han B, Zheng R, Zeng H, et al. Cancer incidence and mortality in China, 2022[J]. J Natl Cancer Cent, 2024, 4(1): 47-53.
[2]
Guinney J, Dienstmann R, Wang X, et al. The consensus molecular subtypes of colorectal cancer[J]. Nat Med, 2015, 21(11): 1350-1356.
[3]
Popat S, Hubner R, Houlston RS. Systematic review of microsatellite instability and colorectal cancer prognosis[J]. J Clin Oncol, 2005, 23(3): 609-618.
[4]
Taieb J, Zaanan A, Le Malicot K, et al. Prognostic effect of BRAF and KRAS mutations in patients with stage Ⅲ colon cancer treated with leucovorin, fluorouracil, and oxaliplatin with or without cetuximab: a post hoc analysis of the PETACC-8 Trial[J]. JAMA Oncol, 2016, 2(5): 643-653.
[5]
Overman MJ, Ernstoff MS, Morse MA. Where we stand with immunotherapy in colorectal cancer: deficient mismatch repair, proficient mismatch repair, and toxicity management[J]. Am Soc Clin Oncol Educ Book, 2018, 38: 239-247.
[6]
Gunderson LL, Jessup JM, Sargent DJ, et al. Revised TN categorization for colon cancer based on national survival outcomes data[J]. J Clin Oncol, 2010, 28(2): 264-271.
[7]
Gray R, Barnwell J, McConkey C, et al. Adjuvant chemotherapy versus observation in patients with colorectal cancer: a randomised study[J]. Lancet, 2007, 370(9604): 2020-2029.
[8]
Baxter NN, Kennedy EB, Bergsland E, et al. Adjuvant therapy for stage II colon cancer: ASCO guideline update[J]. J Clin Oncol, 2022, 40(8): 892-910.
[9]
Taieb J, Svrcek M, Cohen R, et al. Deficient mismatch repair/microsatellite unstable colorectal cancer: diagnosis, prognosis and treatment[J]. Eur J Cancer, 2022, 175: 136-157.
[10]
Sinicrope FA, Foster NR, Thibodeau SN, et al. DNA mismatch repair status and colon cancer recurrence and survival in clinical trials of 5-fluorouracil-based adjuvant therapy[J]. J Natl Cancer Inst, 2011, 103(11): 863-875.
[11]
Zhang X, Wu T, Cai X, et al. Neoadjuvant immunotherapy for MSI-H/dMMR locally advanced colorectal cancer: new strategies and unveiled opportunities[J]. Front Immunol, 2022, 13: 795972.
[12]
Zheng J, Huang B, Nie X, et al. The clinicopathological features and prognosis of tumor MSI in East Asian colorectal cancer patients using NCI panel[J]. Future Oncol, 2018, 14(14): 1355-1364.
[13]
Mei WJ, Mi M, Qian J, et al. Clinicopathological characteristics of high microsatellite instability/mismatch repair-deficient colorectal cancer: a narrative review[J]. Front Immunol, 2022, 13: 1019582.
[14]
Li J, Xu Q, Luo C, et al. Clinicopathologic characteristics of resectable colorectal cancer with mismatch repair protein defects in Chinese population: Retrospective case series and literature review[J]. Medicine (Baltimore), 2020, 99(24): e20554.
[15]
Liang Y, Cai X, Zheng X, et al. Analysis of the clinicopathological characteristics of stage I~III colorectal cancer patients deficient in mismatch repair proteins[J]. Onco Targets Ther, 2021, 14: 2203-2212.
[16]
Lizardo DY, Kuang C, Hao S, et al. Immunotherapy efficacy on mismatch repair-deficient colorectal cancer: From bench to bedside[J]. Biochim Biophys Acta Rev Cancer, 2020, 1874(2): 188447.
[17]
Guan X, Cheng P, Wei R, et al. Enlarged tumour-draining lymph node with immune-activated profile predict favourable survival in non-metastatic colorectal cancer[J]. Br J Cancer, 2024, 130(1): 31-42.
[18]
Han K, Tang JH, Liao LE, et al. Neoadjuvant immune checkpoint inhibition improves organ preservation in T4bM0 colorectal cancer with mismatch repair deficiency: a retrospective observational study[J]. Dis Colon Rectum, 2023, 66(10): e996-e1005.
[19]
Sacdalan DL, Garcia RL, Diwa MH, et al. Clinicopathologic factors associated with mismatch repair status among filipino patients with young-onset colorectal cancer[J]. Cancer Manag Res, 2021, 13: 2105-2115.
[20]
Märkl B, Rößle J, Arnholdt HM, et al. The clinical significance of lymph node size in colon cancer[J]. Mod Pathol, 2012, 25(10): 1413-1422.
[21]
Ruisch JE, Kloft M, Fazzi GE, et al. Large negative lymph nodes - a surrogate for immune activation in rectal cancer patients?[J]. Pathol Res Pract, 2020, 216(9): 153106.
[22]
Märkl B, Schaller T, Kokot Y, et al. Lymph node size as a simple prognostic factor in node negative colon cancer and an alternative thesis to stage migration[J]. Am J Surg, 2016, 212(4): 775-780.
[23]
Wright FC, Law CH, Last L, et al. Lymph node retrieval and assessment in stage II colorectal cancer: a population-based study[J]. Ann Surg Oncol, 2003, 10(8): 903-909.
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