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Chinese Journal of Clinicians(Electronic Edition) ›› 2021, Vol. 15 ›› Issue (11): 833-841. doi: 10.3877/cma.j.issn.1674-0785.2021.11.007

• Clinical Research • Previous Articles     Next Articles

Analysis of clinicopathological characteristics and survival of simultaneous multiple primary colorectal cancer

Xuhua Hu1, Miao Yu2, Penghui Liu3, Jianfeng Zhang1, Baokun Li1, Xiaoran Wang1, Ganlin Guo1, Bin Yu1, Zhenya Zhang1, Guiying Wang4,()   

  1. 1. The 2nd Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050001, China
    2. Basic Medical College, Hebei Medical University, Shijiazhuang 050017, China
    3. The 2nd Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050001, China; Department of Anorectal Surgery, Handan First Hospital, Handan 056001, China
    4. The 2nd Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050001, China; Department of Gastrointestinal Surgery, the Third Hospital of Hebei Medical University, Shijiazhuang 050011, China
  • Received:2021-08-01 Online:2021-11-15 Published:2022-04-02
  • Contact: Guiying Wang

Abstract:

Objective

To investigate the clinicopathological features and long-term survival prognosis of synchronous colorectal carcinoma (sCRC).

Methods

This is a single center retrospective, case-control study to screen the retrospective data cohort of colorectal cancer (CRC) at the Fourth Hospital of Hebei Medical University from January 2017 to December 2019. According to the inclusion and exclusion criteria, 79 patients with multiple primary CRC and 158 patients with single primary CRC were randomly matched at 1∶2 in this cohort. General data, surgical information, complications, lesion distribution, pathological data, and molecular markers were compared between the two groups to screen the characteristic variables of sCRC. The survival outcomes (overall survival [OS] and progression-free survival [PFS]) were recorded and compared between the two groups. Subgroup analysis was also performed.

Results

(1) In the multiple primary CRC group, the percentages of patients with adenoma (χ2=22.937, P<0.001), male patients (χ2=6.722, P=0.010), and those with hypoproteinemia (χ2=10.621, P=0.001), anemia (χ2=13.709, P<0.001), incomplete colonoscopy (χ2=12.253, P<0.001), and microsatellite instability (MSI) (χ2=14.719, P=0.001) were higher than those in the single primary CRC group. There were no significant differences in gender, age, BMI, family history, CEA, operation mode, anastomotic leakage, intestinal obstruction, TNM stage, lymph node metastasis, vascular tumor thrombus, nerve invasion, KRAS status or BRAF status between the two groups (P>0.05). (2) There were 68 cases with double lesions, 10 with three lesions, 1 with four lesions in sCRC, including 50 lesions in the right colon (29.41%) and 120 lesions in the left colon (70.59%). Compared with the single primary CRC group (17.72% of lesions in the right colon and 82.28% in the left colon), the proportion of lesions in the right colon in the multiple primary CRC group was significantly higher in the multiple primary CRC group (χ2=6.174, P=0.013). (3) The median follow-up time was 23.1 months, with 7 cases (2.95%) lost to follow-up. The 1-, 2-, and 3-year survival rates were 96.0%, 90.6%, and 87.5% in the multiple primary CRC group, and 94.6%, 87.5%, and 84.6% in the single primary CRC group; there was no significant difference between the two groups (P=0.76). The PFS interval was 0-44.5 months, with an average of 20.6 months. There was no significant difference in PFS between the two groups (P=0.14). (4) Subgroup analysis showed that there was no significant difference in OS among subgroups (P>0.05). In the multiple primary CRC group, PFS in the multiple adenoma subgroup (hazard ratio [HR]=0.34, 95% confidence interval [CI]: 0.12-0.96, P=0.042), stages 0-Ⅱ subgroup (HR=0.20, 95%CI: 0.05-0.76, P=0.019), and stage Ⅳ subgroup (HR=0.15, 95%CI: 0.04-0.66, P=0.012) were worse than that of the single primary CRC group.

Conclusion

sCRC is characterized by adenoma, hypoproteinemia, anemia, male predisposition, high proportion of incomplete colonoscopy, and high proportion of MSI. The tumor is often located in the right colon. There is no difference in OS and PFS between sCRC and single primary CRC, but PFS may be worse in sCRC patients with multiples adenoma and stage 0-Ⅱ and stage Ⅳ disease.

Key words: Multiple primary, Colorectal cancer, Pathological features, Overall survival, Disease free survival

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