Pubmed | Biomarker | Relation | Statistics | Odds (95% CI) |
P-value | Description | |
---|---|---|---|---|---|---|---|
34109467 | HE4 | high-risk group | p<0.001 | Serum HE4 levels was significantly associated with high-risk group | |||
28751757 | L1CAM | low-risk histology classification | p<0.001 | Patients with high L1CAM expression in curettage specimen had significantly higher occurrence of lymph node metastases compared with patients with low expression of L1CAM in the subgroup with low-risk histology classification (30% vs 9% respectively | |||
28618925 | DJ-1 | high-risk group | 1073 vs 444 pg/mL | 1073 vs 444 pg/mL | p≤0.05 | DJ-1 levels were significantly higher in high-risk EC versus low-risk EC | |
28618925 | DJ-1 | low-risk group | 350 ± 76 vs 602 ± 86 pg/mL | 350 ± 76 vs 602 ± 86 pg/mL | p≤0.05 | Among the low-risk group, DJ-1 serum levels were significantly higher in patients with MI ≥ 50% compared to patients with MI < 50% | |
27038842 | CD103 | high-risk adenocarcinoma patients | p=0.031 | The presence of a high CD103+ cell infiltration was associated with an improved prognosis in patients with endometrial adenocarcinoma .This beneficial effect was particularly evident in high-risk adenocarcinoma patients | |||
26743472 | L1CAM | high-risk group | p<0.001 | L1CAM positivity was associated with high-risk endometrial cancer | |||
26554657 | CDK4/6 | low-risk patient | p=0.002 | CDK4/6SA was significantly higher in pathologically low-risk patients (not receiving adjuvant chemotherapy, n=74) than in intermediate- or high-risk patients (receiving adjuvant chemotherapy, n=35). | |||
26554657 | CDK4/6 | intermediate-/high-risk group/survival | p=0.063 | In the intermediate-/high-risk group, patients with high CDK4/6SA had a tendency of a more favourable prognosis compared with patients with low CDK4/6SA | |||
26223178 | HE4 | high-risk patients | 0.77 for HE vs 0.71 for CA125 | 0.77 for HE vs 0.71 for CA125 | The cut-off 76.5 pmol/L is a better predictor in distinguishing the high-risk patients than CA125 better predictor in distinguishing the high-risk patients than CA125 | ||
26223178 | HE4 | discrimination | p<0.001 | In the case of HE4, there was a statistically significant difference between patients with low and high risk of the disease. | |||
26045311 | MTV | myometrial invasion/high risk | OR of 7.3 (CI, 2.9–18.3) | p<0.001 | adjusting for preoperative biopsy results suggesting high risk (nonendometrioid subtype or endometrioid grade 3), an MTV cutoff of 20 mL yielded an OR of 7.3 (CI, 2.9–18.3; P < 0.001) for deep invasion | ||
34099314 | glycine | endometrial cancer risk | OR1SD: 0.89, 95% CI: 0.80-0.99; | Glycine was inversely associated with endometrial cancer risk | |||
26045311 | MTV | high risk | OR of 10.9 (CI, 2.1–55.3; | p<0.005 | adjusting for preoperative biopsy results suggesting high risk (nonendometrioid subtype or endometrioid grade 3),MTV cutoff of 30 mL yielded an OR of 10.9 (CI, 2.1–55.3; P < 0.005) for lymph node metastases. | ||
25275055 | Intraepithelial CD3(+) TIL counts | risk groups | HR=4.56, 95% CI=1.77-11.75 | p=0.002 | In multivariate analysis of patients with early tumors that included the TIL populations investigated and risk groups (high risk vs. low risk), intraepithelial CD3+ TIL counts below 17 per mm2 were associated with inferior prognosis | ||
23266443 | ERα/ERβ1 expression ratios | risk | HR, 6.4 [95% CI, 1.0-40.6; | p=.04 | An ERα/ERβ1 ratio of 1 or less has proved to be independently associated with a higher risk of death along with age, tumor stage, and Ki-67. | ||
23266443 | ERα/ERβ2 expression ratios | risk | HR,9.7 [95% CI, 1.1-85.3; | p=.04 | An ERα/ERβ2 ratio of 1 or less has proved to be independently associated with a higher risk of death respectively along with age, tumor stage, and Ki-67. | ||
22889453 | HSPA5 | high-risk endometrial cancer | p=0.007 | The positive rate of HSPA5 was higher in high-risk EC tissue than in low-risk EC and normal endome-trial tissue (77.2% [44/57] versus 53.2% [33/62] and45.0% [9/20], | |||
22644303 | pHH3 | risk stratification | p<0.0001 | The rate of pHH3-positive cells was significantly associated with risk stratification | |||
21242118 | Stathmin | low-risk | sensitivity = 0.44, specificity = 0.70, PPV = 0.13, and NPV = 0.92 | sensitivity = 0.44, specificity = 0.70, PPV = 0.13, and NPV = 0.92 | OR = 1.82 (95% CI: 0.93–3.57), | Analyzing Stathmin expressions in curettage specimens in the low-risk curettage group separately, the multivariate OR is 1.82 (95% CI: 0.93–3.57), sensitivity = 0.44, specificity = 0.70, PPV = 0.13, and NPV = 0.92 | |
8088605 | CA 125 | high-risk patients | p=0.0026 | Low-risk patients (G1 and M0-M1 tumors) showed a CA 125 positivity (> 35 U/ml) of 10% with respect to 37% of high-risk patients (G2-G3 and M2 tumors) | |||
34802721 | C-reactive protein | p < 0.05 | Women with pre-treatment CRP ≥5.5 mg/L had a 68% increase in overall (adjusted HR = 1.68, 95% CI 1.00-2.81, p = 0.049) and a two-fold higher cancer-specific mortality risk than those with CRP <5.5 mg/L (adjusted HR = 2.04, 95%CI 1.03-4.02, p = 0.04). | ||||
36251972 | p53 | risk | P <0.001 | Abnormal p53 IHC expression was expressed in 33.3% of the cases and significantly associated with the tumor grade, myometrial invasion (MI), lymphovascular invasion (LVSI), nodal metastasis, and FIGO stage, and the advanced European Society for Medical Oncology (ESMO) risk groups. | |||
34099314 | serine | endometrial cancer risk | OR1SD: 0.89, 95% CI: 0.79-1.00 | Serine was inversely associated with endometrial cancer risk | |||
36251972 | Pirh2 | high-risk group | P =0.005 | High IHC Pirh2 expression was noted in 58.3% of the cases, and significantly associated with high-risk group. | |||
36251972 | L1CAM | high-risk group | P =0.002 | Positive L1CAM immunoexpression was noted in 26.7% and was significantly associated with high-risk group. | |||
36690721 | ER | low-risk group | Subgroup-analysis showed that only in NSMP HR-EC, ER-positivity was independently associated with a reduced risk of recurrence (HR 0.33, 95%CI 0.15-0.75). | ||||
34099314 | SM C18:0 | endometrial cancer risk | OR1SD: 1.18, 95% CI: 1.05-1.33 | Sphingomyelin [SM] C18:0 was inversely associated with endometrial cancer risk | |||
34099314 | free carnitine | endometrial cancer risk | OR1SD: 0.91, 95% CI: 0.81-1.00 | Free carnitine (C0) was inversely associated with endometrial cancer risk | |||
33237570 | P53 | risk | [OR] 1.799, 95%CI 1.033–3.133, | p=0.038 | The high P53 index (>67%) was found to be an independent risk factor for the recurrence of endometrial cancer in multivariate Cox regression analysis, eliminating the effects of other factors | ||
33197888 | PPARγ(-)/ERRα(+) | risk factor | OR=14.847, 95% CI= 1.6-137.748 | p=0.018 | A PPARγ/ERRα ratio≤1.86 was an independent risk factor for endometrial carcinogenesis | ||
29114696 | cancer antigen 15-3 levels | low-risk patient | (16.2±7.1 [4.0-32.0] IU/mL vs 24.4±18.2 [4.0-153.0] IU/mL). | (16.2±7.1 [4.0-32.0] IU/mL vs 24.4±18.2 [4.0-153.0] IU/mL). | 95% confidence interval: 0.57−0.79 | p=0.03 | the mean serum CA15-3 levels were lower in low-risk patients compared to other patients with ECs |
28751757 | L1CAM | low-risk group | High expression of L1CAM in curettage specimen predicted poor disease-specific survival in within patients with low-risk curettage histology |