Prediction of biological behavior and prognosis of colorectal cancer patients by tumor MSI/MMR in the Chinese population.

Colorectal cancers (CRCs) exhibiting microsatellite instability (MSI) have special biological behavior. The clinical predictors for MSI and its survival relevance for the Chinese population were still unclear. Seven hundred ninety-five CRC patients were retrospectively assessed. Mismatch repair (MMR) proteins (MSH2, MSH6, PMS1, and MLH1) expression was detected by immunohistochemistry using tumor tissues of all patients. DNA MSI status was analyzed by polymerase chain reaction in 182 samples randomly selected from the 795 cases. Among all CRC tumor tissues, 97 cases (12.2%) were with an MMR protein-deficient (MMR-D) phenotype, whereas 698 cases (87.8%) were with an MMR proteins intact (MMR-I) phenotype. A total of 21 (11.5%) CRCs were identified as having high microsatellite instability, 156 (85.7%) tumors were having microsatellite stability (MSS), and five (2.7%) were having low microsatellite instability. Importantly, MMR status was demonstrated to be moderately consistent with MSI status (κ=0.845, 95% confidence interval [CI] 0.721, 0.969). Unconditional logistic regression analysis revealed age, number of lymph node, tumor diameter, and tumor site as predictors for MSI with a substantial ability to discriminate different MSI status by area under curve of 80.62% using receiver operation curve. Compared with MMR-I, MMR-D was an independent prognostic factor for longer overall survival (hazard ratio =0.340, 95% CI 0.126, 0.919; P=0.034). MMR-D is an independent prognostic factor for better outcome. Our results may provide evidence for individualized diagnosis and treatment of CRC, but this will require further validation in larger sample studies.

Introduction

Colorectal cancer (CRC) is the third most commonly diagnosed cancer globally.1 In China, the incidence and mortality of CRC continues to rise, both of which rank the fifth place among malignant tumors, mainly due to the adoption of Western lifestyle and the aging of the population.2 According to molecular phenotypes, CRC are classified as CMS1, CMS2, CMS3, CMS4, and “others”. CMS1 tumors are 14% of CRCs and represent as hypermutated, microsatellite unstable, and with strong immune activation. CMS2 (canonical, 37%) presents as epithelial, chromosomally unstable, with marked WNT and MYC signaling activation. CMS3 (metabolic, 13%) presents as epithelial, with evident metabolic dysregulation. CMS4 (mesenchymal, 23%) has prominent transforming growth factor β activation, strong invasiveness, and angiogenesis. And “others” (with mixed features, 13%) represent a transition phenotype or intratumoral heterogeneity.3 Precise molecular phenotype classification of CRC may contribute significantly to personalized prognosis and therapy.

Microsatellite instability (MSI), mainly due to mismatch repair (MMR) system defection, accounts for ~15% of CRCs. About 80% of MSI CRCs are sporadic colorectal cancer, and the others are hereditary nonpolyposis colorectal cancer (HNPCC).4 The main function of the MMR system is to identify and repair the mismatches that occurred during DNA replication, therefore ensuring genomic conservation and stability. The most common MMR genes are MSH2, MSH6, PMS2, and MLH1. MSI is classified into high (MSI-H), low (MSI-L), and stable (MSS) types by analyzing the microsatellite status.5 According to the expression of the MMR proteins, tumors are classified into two types: MMR proteins deficient (MMR-D) and MMR proteins intact (MMR-I).5 Patients with MSI-H CRC have distinct clinicopathological characteristics, compared with patients with MSS/MSI-L phenotype. MSI-H CRCs are more common in females, tend to have proximal location, poorly differentiated mucinous phenotype, and increased rates for peritumoral and intratumoral lymphocytic infiltration.6

MSI analysis by polymerase chain reaction (PCR) is the gold standard technique for assessing microsatellite status. The American National Cancer Institute recommended five DNA markers for MSI test,7 including BAT25, BAT26, D2S123, D5S346, and D17S250. A tumor can be defined as MSI-H, when two or more of the five markers in the tumor DNA are tested positive. The tumor is defined as MSI-L if only one marker is tested positive, and MSS if all five markers are tested negative. In addition, the status of MMR defection can also be detected by examining the loss of MMR proteins expression via immunohistochemical (IHC) analysis.

Great difference in patterns of MMR gene mutations was observed among patients with different ethnicity and geography. The MSH2 gene has the highest mutant frequency in European and American populations, whereas MLH1 mutation was predominant in those from Japan and South Korea.8 MSH2 and MSH6 gene mutations occurred most frequently in Australians.9 The percentage of right colon cancer and mucinous adenocarcinoma in the Chinese population was lower than the Caucasian population, and there was great disparity in the microsatellite status between Chinese and Western populations.10,11 Few studies have focused on the relationship between MMR and MSI in China, and the clinical outcome relevance of MMR/MSI in Chinese population is still unclear. In order to find out the role of MSI and MMR system in Chinese CRC patients, this study first investigated the consistency in the technology matters (eg, sensitivity and specify) between PCR and IHC, and second, revealed the association of MMR defection with patients’ outcome.

Materials and methods

Patients

We retrospectively identified 795 patients who had CRC surgery at the Affiliated Drum Tower Hospital of Nanjing University Medical School between January 2012 and July 2015, who then were enrolled as subjects in this study. This study was approved by the Medical Ethics Committee of the Affiliated Drum Tower Hospital of Nanjing University Medical School and all participants provided written informed consent. All patients satisfied the following criteria: they had 1) sporadic colon or rectal cancer confirmed by pathological diagnosis, 2) no preoperative therapy, including preoperative radiotherapy in the rectal cancer patients, 3) received radical resection or a palliative operation, and 4) clinical and pathological data available that can be extracted for analysis.

Exclusion criteria were 1) tumors in the appendix and anal canal; 2) genital tumor; 3) second primary tumor out of colorectal; 4) squamous cell carcinoma, melanoma, and gastrointestinal stromal tumor; and 5) in situ carcinoma (high-grade intraepithelial neoplasia).

Follow-up data were retrieved from medical records and confirmed by direct interviews with the patients’ physicians or family members. Overall survival (OS) was defined as the interval between surgery and date of death. Progression-free survival (PFS) was the interval between surgery and recurrence or detection of metastasis. The postoperative period was measured from the surgery date to the time of the last follow-up or death. At the end of the study (January 2016), the median follow-up time for all patients was 15 months (range: 1–48 months).

Tumor MMR proteins expression detected by IHC

We conducted IHC analysis of MSH2, MSH6, PMS2, and MLH1 proteins with formalin-fixed paraffin-embedded tumor samples. After the tumor area adjacent to normal mucosa and/or lymphocytic infiltration was marked, 4 mm of paraffinized tissue was removed, and multiple tissue blocks were prepared. Finally, 4-µm thick sections were obtained for IHC following standard protocols. The mouse monoclonal antibodies used were anti-MSH2, anti-MSH6, anti-MLH1, and anti-PMS2 (BD Pharmingen). Adjacent normal tissues from each sample served as positive controls (Figure 1).

Figure 1

Immunohistochemical profile of mismatch repair gene protein.

Notes: (A) MLH1 negative (×200). (B) PMS2 negative (×200).

Tumor MSI analysis detected by PCR

For microsatellite analysis, DNA was extracted from formalin-fixed paraffin-embedded tissue with QIAamp Tissue kit (Qiagen) according to the manufacturers’ instructions. MSI status was evaluated with five microsatellite markers (BAT25, BAT26, D2S123, D5S346, and D17S250) using fluorescence-based PCR. DNA samples from tumor tissues and normal tissues were amplified in a 20 µL volume containing 100 ng of DNA, 1 µmol/L of dye-labeled forward and unlabeled reverse primers, 200 µmol/L of deoxynucleotide, 1.5 mmol/L of MgCl2, and 0.75 U of Taq DNA polymerase. The PCR was performed under the following conditions: denaturation at 95°C for 5 minutes, 35 cycles of denaturation at 95°C for 30 seconds, annealing at 53°C for 30 seconds, and extension at 72°C for 30 seconds. Final extension was at 72°C for 10 minutes (Figure 2).

Figure 2

Images of separation of multiplex-amplified Bethesda loci (BAT25, BAT26, D2S123, D5S346, and D17S250).

Notes: (A) Normal amplification of all the five loci. (B) Representative image showing MSI-L. (C) Representative image showing MSI-H with arrows indicating instability.

Abbreviations: MSI-H, microsatellite instability high; MSI-L, microsatellite instability low; MSS, microsatellite stable.

PCR product was analyzed by a genetic analyzer (Applied Biosystems 3500, ABI). Raw data were analyzed using GeneMapper 4.1 software. Patients were categorized as MSI-H if any two or more of the five studied markers showed positivity, MSI-L if only one marker showed positivity, and MSS if all markers showed negativity.

Statistical methods

All statistical calculations were performed using SAS version 9.4 software (SAS Institute Inc., Cary, NC, USA). Unconditional logistic regression was used to identify potential predictors for MSI. Optimal cutoff value of each predictor was coded as c. The risk score was denoted as s and calculated as follows: where i is the ith patient, and j is the jth clinical factor. To investigate the predictive value of clinical factors for MSI, we constructed a formula calculating the risk score function (RSF), according to the liner combination of the factors weighted by a univariate logistic regression coefficient. The RSF for the patient i was calculated as follows: where W is the weight of the jth clinical factor described previously. Then the RSF was analyzed as a continuous variable enrolling to the receiver operating curve (ROC). The area under the ROC curve (AUC) was used to estimate the predictive value of the clinical factors for MSI. PFS and OS were compared using the Kaplan–Meier method with a log-rank test. Risk of disease progression and death was calculated with Cox proportional hazards regression model. Differences were taken as significant when two-tailed P-value was <0.05.

Results

Clinicopathological features of CRC

A total of 795 CRC cases were included in this study; 482 of the patients (60.6%) were males. Their age ranged from 15 to 91 years, and the median age of onset was 63 years. The location of primary tumors included proximal colon (30.4%), distal colon (30.4%), and the rectum (39.2%). The clinicopathological data are summarized in Table 1.

Table 1

Clinicopathological information of the studied patients

Clinical feature	n (%)
Gender
Male	482 (60.6)
Female	313 (39.4)
Age (years)
≤60	322 (40.5)
>60	473 (59.5)
Location
Proximal	242 (30.4)
Distal	242 (30.4)
Rectum	311 (39.2)
TNM stages
I	87 (10.9)
II	307 (38.6)
III	357 (44.9)
IV	44 (5.6)
Tumor grade
G1	208 (26.2)
G2	547 (68.8)
G3 + G4	40 (5.0)
Histology type
Mucinous	116 (14.6)
Nonmucinous	679 (85.4)

Frequency of the loss of MMR proteins expression and MSI status

MMR proteins of all samples were detected by IHC. If all of the four MMR proteins were positively expressed, tumor was defined as MMR-I. Otherwise, it was defined as MMR-D. In all CRC tumor tissues, 97 cases (12.2%) were of MMR-D phenotype, and 698 cases (87.8%) were of MMR-I phenotype. In the MMR-D group, one protein expression loss occurred in 56 cases (57.7%), two proteins expression loss in 31 cases (32.0%), and three proteins expression loss in 7 cases (7.2%). Only three cases (3.1%) were observed, whose tumor had no expression for all of the four MMR proteins. The frequency of expression loss was identified in each of the four MMR proteins: MLH1 (6.3%), MSH2 (2.6%), MSH6 (3.0%), and PMS2 (7.3%). MSI status of 182 samples that selected randomly from all patients was detected by PCR. Twenty-one tumors (11.6%) were with MSI-H phenotype, 5 (2.7%) were with MSI-L, and 156 (85.7%) were with MSS. The frequency of each MSI marker positives is listed in Table 2.

Table 2

The frequency of each microsatellite instability marker positive in the Bethesda panel

MSI status	Microsatellite instability markers
	BAT25	BAT26	D2S123	D5S346	D17S250
MSI-H	14	8	12	6	10
MSI-L	0	0	2	1	2
Total	14	8	14	7	12

Abbreviations: MSI, microsatellite instability; MSI-H, microsatellite instability high; MSI-L, microsatellite instability low.

Consistency between IHC and PCR methods to detect the status of MSI

PCR is the gold standard technique for MSI detection12,13 (Table 3). We compared the MSI status and MMR protein expression to evaluate the accuracy of IHC results in discriminating MSI. The sensitivity and specificity of the method of IHC assay were 82.6% (19/23) and 98.7% (157/159), respectively (Table 4). The κ value of the two methods was 0.845 (95% confidence interval [CI] 0.721,0.969), indicating a moderate consistency between the two methods.

Table 3

Clinicopathological characteristics of the MMR-I and MMR-D groups

	Proximal colon		P-value	Distal colon		P-value	Rectum		P-value
	MMR-I	MMR-D		MMR-I	MMR-D		MMR-I	MMR-D
Gender			0.545			0.912			0.900
Male	121	24		136	12		168	21
Female	78	19		86	8		109	13
TNM stages			0.002			0.874			0.002
I + II	92	31		104	9		132	26
III + IV	107	12		118	11		145	8
Tumor grades			0.243			0.557			0.085
G1	10	5		11	0		13	1
G2	131	25		155	13		194	29
G3 + G4	58	13		56	7		70	4
Histological types			0.699			0.712			0.562
Mucinous	41	10		27	3		30	5
Nonmucinous	158	33		195	17		247	29
Lymph nodes metastasis			0.002			1.000			0.002
Negative	92	31		104	9		132	26
Positive	107	12		118	11		145	8

Abbreviations: MMR-D, mismatch repair proteins deficient; MMR-I, mismatch repair proteins intact.

Table 4

Correlation between the PCR method and the IHC array for MSI status in tumors of 182 CRC patients

	MMR-D (n)	MMR-I (n)	Total	Kappa consistency test
MSI-H (n)	19	2	21	0.845 (0.721, 0.969), P<0.001
MSS and MSI-L (n)	4	157	161
Total	23	159	182

Abbreviations: CRC, colorectal cancer; IHC, immunohistochemistry; MMR-D, mismatch repair proteins deficient; MMR-I, mismatch repair proteins intact; MSI, microsatellite instability; MSI-H, microsatellite instability high; MSI-L, microsatellite instability low; MSS, microsatellite stable; PCR, polymerase chain reaction.

Difference in clinicopathological characteristic between the MMR-I and MMR-D groups in proximal colon, distal colon, and rectal cancers

We found that in proximal colon and rectal cancers, tumors with an MMR-I phenotype were more likely to be of later stage (53.8% vs 27.9% and 52.3% vs 23.5%, respectively) and have a lower percentage of lymph nodes metastasis (46.2% vs 72.1% and 47.7% vs 76.5%, respectively). However, we could not detect the significant difference in the distribution of stage and lymph nodes metastasis between distal colon tumors with different MSI status (Table 3).

Predictors of MSI based on the clinical factors

Unconditional logistic regression revealed that younger age (odds ratio [OR] =0.970, P=0.034), fewer involved lymph nodes (OR =0.244, P=0.003), lager tumor diameter (OR =1.434, P<0.001), and proximal colon lesions (OR =0.361, P<0.001) were predictors for MSI, and the increased risk of MSI in the presence of these predictors held when gender, tumor stage, and tumor difference were adjusted as covariates in the logistic regression model (Table 5).

Table 5

Logistic regression models to find out predictors for MSI

Factors	OR (95% CI), P-value	Adjusted OR (95% CI), P-value (multivariate)
Age	0.970 (0.943, 0.988), 0.034	0.971 (0.943, 0.999), 0.043
Gendera	0.600 (0.273, 1.319), 0.204	0.617 (0.256, 1.486), 0.282
Tumor diameter	1.434 (1.211, 1.698), <0.001	1.300 (1.076, 1.572), 0.007
Tumor siteb	0.361 (0.207, 0.631), 0.0004	0.419 (0.223, 0.784), 0.007
No of lymph node	0.244 (0.096, 0.619), 0.003	0.257 (0.056, 1.185), 0.082
Differencec	0.746 (0.457, 1.218), 0.241	0.798 (0.462, 1.380), 0.420
Stage	0.641 (0.392, 1.047), 0.076	0.923 (0.344, 2.576), 0.874

Notes:

Female is the reference.

It was defined as 1, 2, 3 enrolling to logistic regression model. The corresponding site is proximate colon site, distal colon site, and rectum.

It was defined as 1–5 enrolling to logistic regression model. The corresponding difference level is from poor differentiation to high differentiation.

Abbreviations: CI, confidence interval; MSI, microsatellite instability; OR, odds ratio.

We used RSF weighed by coefficient of logistic regression to construct an ROC curve (Figure 3). An 80.62% of AUC was observed, indicating that the combination of these predictors being highly efficient can identify potential CRC populations with MSI.

Figure 3

ROC curves for the predictive ability of clinical factors for microsatellite instability status.

Abbreviation: ROC, receiver operating characteristic curve.

The role of MMR proteins expression and MSI status in prognosis of CRC patients

Of all the patients, 711 patients were followed up by a median time of 15 months. A total of 166 patients (23.3%), composed of 154 MMR-I and 12 MMR-D phenotype patients, had developed distant metastases and/or local recurrence. Sixty-eight patients (9.6%) died, including 63 with the MMR-I and five with the MMR-D phenotype. Patients with MSI-H had longer PFS than those with MSS/MSI-L (log-rank test: P=0.023), although there was no significant difference in OS (Figure 4). In consistent with the MSI-based results, patients with MMR-D also had longer PFS and OS compared with those with MMR-I (log-rank test: PFS, 38.16 vs 29.12 months, P=0.0011 and OS, 40.20 vs 35.13 months, P=0.013; Figure 4). In the multivariate analysis, MMR-D was also found to be a significant indicator for OS, after adjustment for age, gender, TNM stage, tumor grade, tumor differentiation, tumor diameter, and tumor size (hazard ratio [HR] =0.340, 95% CI 0.126, 0.919; P=0.034; Table 6).

Figure 4

PFS and OS in all patients.

Notes: (A and B) PFS and OS according to MSI status in all patients. The red line is MSI-H. The blue line is MSS/MSI-L. (C and D) PFS and OS according to MMR proteins expression in overall patients. The red line is MMR-D. The blue line is MMR-I.

Abbreviations: MMR, mismatch repair gene; MMR-D, mismatch repair proteins deficient; MMR-I, mismatch repair proteins intact; MSI, microsatellite instability; MSI-H, microsatellite instability high; MSI-L, microsatellite instability low; MSS, microsatellite stable; PFS, progression-free survival; OS, overall survival.

Table 6

Cox’s proportional hazards regression model for the correlation of MMR status with PFS and OS

Patients	PFS				OS
	HR (95% CI)	P-value	Adjusted HR(95% CI)	P-value	HR (95% CI)	P-value	Adjusted HRa(95% CI)	P-value
Overall		0.015		0.088		0.012		0.034
MMR-D	0.442 (0.229–0.852)		0.547 (0.274–1.093)		0.300 (0.118–0.766)		0.340 (0.126–0.919)
MMR-I	References
Stages II–III		0.030		0.011		0.017		0.007
MMR-D	0.464 (0.232–0.926)		0.402 (0.198–0.813)		0.282 (0.100–0.797)		0.231 (0.079–0.673)
MMR-I	–

Note:

Adjusted for age, gender, TNM stage, tumor grade, and tumor diameter.

Abbreviations: CI, confidence interval; HR, hazard ratio; MMR, mismatch repair gene; MMR-D, mismatch repair proteins deficient; MMR-I, mismatch repair proteins intact; OS, overall survival; PFS, progression-free survival.

Survival analysis was also conducted in the stage-based subgroups. Consist with the overall results, MSI-H had no impact on OS in stages II–III patients (log-rank test: P=0.390). However, the overall result that MSI-H was a predictor for prolonged PFS became insignificant when data were limited to stages II–III patients (log-rank test: P=0.136; Figure 5). Because statistical power was largely decreased by subgroup analysis, we regarded this inconsistency with overall results as a bias caused by reduced sample size. However, it was revealed that stages II–III patients with MMR-D had longer OS and PFS, when compared with those with MMR-I (log-rank test: OS, P=0.011; PFS, P=0.025; Figure 5). Importantly, MMR-D was also an independent predictor for longer PFS (HR =0.402, 95% CI 0.198, 0.813; P=0.011) and OS (HR =0.231, 95% CI 0.079, 0.673; P=0.007), according to the multivariate COX regression analysis (Table 6).

Figure 5

PFS and OS in patients with stages II–III.

Notes: (A and B) PFS and OS according to MSI status in patients with stages II–III. The red line is MSI-H. The blue line is MSS/MSI-L. (C and D) PFS and OS according to mismatch repair gene proteins expression in patients with stages II–III. The red line is MMR-D. The blue line is MMR-I.

Abbreviations: MMR-D, mismatch repair proteins deficient; MMR-I, mismatch repair proteins intact; MSI, microsatellite instability; MSI-H, microsatellite instability high; MSI-L, microsatellite instability low; MSS, microsatellite stable; PFS, progression-free survival; OS, overall survival.

Discussion

MSI is a change in DNA sequence of any length due to either insertion or deletion of repeating units in the genome.7 Because of the application of MSI for screening HNPCC, it has been paid more and more focus on studies in CRC. It may be used as a marker to select stage II CRC patients who will benefit from 5-fluorouracil adjuvant chemotherapy.14 Recent studies indicated that MSI status might be a particular candidate biomarker for checkpoint immunotherapy in CRC because patients with an MMR-D phenotype could benefit from immune checkpoint blockade with pembrolizumab.15,16 Three methods – IHC, PCR, and DNA sequencing – can be used to identify the MSI status of CRC. The IHC method can be used to detect the loss of expression of MMR proteins in the tumor tissue with lower cost and less difficulty. However, only a limited number of MMR proteins can be detected, and the results greatly depend on the individual pathologist. PCR is considered as the “gold standard” for the identification of MSI phenotype.12,13 It also has the advantage of having high reproducibility. DNA sequencing can be used to assess MSI status by detecting the mutations in the genes of enzymatic DNA repair, and it is the only way to identify novel mutations.17 However, DNA sequencing is time consuming, expensive, and requires specialized equipment. Therefore, a more accuracy and cost-effective test protocol is expected to arise from a combination of these methods. In our study, in consistent with previous studies,18–20 there was a moderate consistency between the IHC method for MMR detection and the PCR method for MSI assessment, indicating that combining the results of the IHC and PCR methods is a feasible strategy to obtain more promising results than that of considering either method alone. However, some tumors were MSI-H, but were classified as MMR-D, and some MSS were classified as MMR-D by IHC. Therefore, to get a more accurate determination of MSI status by IHC instead of PCR, additional markers should be tested, such as some other microsatellite loci (D18S65, D18S69, D17S1176, D17S796, D8S261, D8S254, and D8S550).21 Moreover, DNA sequencing may also be helpful in combination with PCR and IHC to produce more reliable results.

Studies showed that MSI tumors were more commonly located in the proximal colon.6,22 In this study, we also found that MMR-D and MSI-H type tumors predominantly occurred in the proximal colon. Moreover, we compared the clinicopathological factors of MMR-D and MMR-I type tumors in proximal colon, distal colon, and rectal cancers. In the proximal colon and rectal cancers, patients with the MMR-I type were found to be tilted to have later stage and have more lymph node metastasis. These different features may arise from a different carcinogenic pathway. There are some studies which reported that tumors with different MMR status may differ in the distribution of age, T stage, N stage, and different gender.22–24

We revealed that age, lymph node, tumor diameter, and tumor location were predictors for increased risk of MSI, and the increased risk held when gender, tumor stage, and tumor difference were adjusted. This result might help us to identify patients whose DNA MSI status are needed to be tested. Previous studies on the prognostic value of MSI for CRC patients have had controversial results.19,20,25–30 Patients inclucded in these studies were from Western-based populations. Although there were a few studies focusing on MSI/MMR in Chinese population,25,31–33 the prognostic relevance of MMR and MSI are still unclear. In our study, with a substantial amount of sample size, we found that MMR proteins expression was an independent factor for prolonged PFS and OS. Studies showed that MSI and MMR had unequal prediction ability for prognosis in patients with different stages. It was indicated that MSI-H tumors was an indicator of good prognosis in stages II and III CRC patients, but survival cannot be significantly prolonged in the context of MSI-H in stage IV patients.21,34–37 Consistent with the previous findings, we also found that MMR-D was a marker for good prognosis in stages II and III. However, due to limited sample size, the prognostic value of MMR-D in stage IV patients could not be statistically calculated.

There are some limitations in this study. Only 68 patients achieved the end of survival events, indicating the limitation of a short follow-up time. These patients will continue to be followed up, and the survival data will be reanalyzed in the next study. Another limitation is the lack of the therapeutic information in this study, making us unable to clarify the interactive effect of therapy and MSI/MMR status on clinical outcome.

Conclusion

MMR protein expression detected by IHC has a moderate consistency with PCR in discriminating MSI status in CRC tumors. Age, lymph node, tumor diameter, and tumor location are strong predictors for DNA MSI status. MMR-D is an independent favorable prognostic factor for primary CRC patients. Our results may provide evidence for individualized diagnosis and treatment according to MSI status-based prediction, if validated by larger studies.