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Table 2 Clinicopathological factors in the L-OHP (+) and (−) groups before and after propensity score matching

From: Significance of postoperative adjuvant chemotherapy with an oxaliplatin-based regimen after simultaneous curative resection for colorectal cancer and synchronous colorectal liver metastasis: a propensity score matching analysis

Clinicopathological factors

Variables

Before matching

p-value

After matching

p-value

L-OHP (+) (n = 47)

L-OHP (−) (n = 47)

L-OHP (+) (n = 21)

L-OHP (−) (n = 21)

Age

Yearsa

61 (32–78)

67 (37–85)

0.02

67 (49–78)

62 (37–82)

0.28

Gender

Male

31 (66.0%)

29 (61.7%)

0.83

17 (81.0%)

15 (71.4%)

0.72

Female

16 (34.0%)

18 (38.3%)

4 (19.0%)

6 (28.6%)

Location

Colon

39 (83.0%)

36 (76.6%)

0.61

17 (81.0%)

15 (71.4%)

0.72

Rectum

8 (17.0%)

11 (23.4%)

4 (19.0%)

6 (28.6%)

Preoperative serum CEA

ng/mLa

38.5 (1.1–3585)

13.6 (2.0–2759)

0.14

12.0 (2.0–442.8)

20.3 (2.6–622.7)

0.62

Preoperative serum CEA

≤ 30.0 ng/mL

22 (46.8%)

33 (70.2%)

0.04

14 (66.7%)

14 (66.7%)

1.00

> 30.0 ng/mL

25 (53.2%)

14 (29.8%)

7 (33.3%)

7 (33.3%)

Preoperative serum CEA

≤ 5.0 ng/mL

10 (21.3%)

8 (17.0%)

0.79

7 (33.3%)

3 (14.3%)

0.28

> 5.0 ng/mL

37 (78.7%)

39 (83.0%)

14 (66.7%)

18 (85.7%)

Postoperative serum CEAb

ng/mLa

2.5 (0.8–115.6)

2.7 (0.4–66.3)

0.94

2.0 (0.9–115.6)

2.4 (0.4–10.9)

0.41

Postoperative serum CEAb

≤ 30.0 ng/mL

41 (91.1%)

43 (95.6%)

0.68

19 (95.0%)

21 (100%)

0.49

> 30.0 ng/mL

4 (8.9%)

2 (4.4%)

1 (5.0%)

0 (0%)

Postoperative serum CEAb

≤ 5.0 ng/mL

30 (66.7%)

37 (82.2%)

0.15

16 (80.0%)

19 (90.5%)

0.41

> 5.0 ng/mL

15 (33.3%)

8 (17.8%)

4 (20.0%)

2 (9.5%)

Differentiation of primary tumor

Differentiated

41 (87.2%)

47 (100%)

0.03

21 (100%)

21 (100%)

1.00

Undifferentiated

6 (12.8%)

0 (0%)

0 (0%)

0 (0%)

T classification

T1–3

37 (78.7%)

27 (57.5%)

0.046

16 (76.2%)

14 (66.7%)

0.73

T4

10 (21.3%)

20 (42.5%)

5 (23.8%)

7 (33.3%)

N classification

N0

15 (31.9%)

11 (23.4%)

0.49

9 (42.9%)

7 (33.3%)

0.75

N1, 2

32 (68.1%)

36 (76.6%)

12 (57.1%)

14 (66.7%)

Number of hepatic lesions

a

2 (1–21)

1 (1–10)

0.04

2 (1–5)

1 (1–6)

0.35

Maximum diameter of hepatic lesion

mma

37 (8–120)

25 (5–85)

0.03

32 (8–65)

30 (8–85)

0.73

Synchronous

Absent

45 (95.7%)

46 (97.9%)

1.00

19 (90.5%)

21 (100%)

0.49

extrahepatic metastasis

Present

2 (4.3%)

1 (2.1%)

2 (9.5%)

0 (0%)

Liver resection

Partial

29 (61.7%)

30 (63.8%)

1.00

17 (81.0%)

13 (61.9%)

0.31

Anatomical

18 (38.3%)

17 (36.2%)

4 (19.0%)

8 (38.1%)

Surgical margin of hepatic lesion

Negative

41 (87.2%)

40 (85.1%)

1.00

19 (90.5%)

18 (85.7%)

1.00

Positive

6 (12.8%)

7 (14.9%)

2 (9.5%)

3 (14.3%)

  1. aMedian (minimum–maximum)
  2. bn = 90 (postoperative serum CEA was not available in four patients)
  3. Univariate analysis indicated that age, preoperative serum CEA (≤ 30.0 ng/mL/ > 30.0 ng/mL), differentiation of primary tumor (differentiated/undifferentiated), T classification (T1-3/T4), number of hepatic lesions and maximum diameter of the hepatic lesion differed significantly between the L-OHP( +) and (−) groups. Patients in the L-OHP (+) group were younger (p = 0.02), more frequently showed preoperative serum CEA of higher than 30.0 ng/mL (p = 0.04), more frequently had an undifferentiated primary tumor (p = 0.03) and a T1–T3 primary tumor (p = 0.046), and had more (p = 0.04) and larger (p = 0.03) hepatic lesions. There were no significant differences in other clinicopathological factors between the two groups
  4. The PS was estimated with potential confounders of age, preoperative serum CEA, differentiation of primary tumor, T classification, number of hepatic lesions, and maximum diameter of hepatic lesions. A total of 21 patients in each group were matched in one-on-one pair PS matching analysis. There were no significant differences in univariate analysis of clinicopathological factors between the L-OHP (+) and (−) groups after PS matching