Retrospective Cohort Study
Copyright ©The Author(s) 2022.
World J Gastrointest Oncol. Sep 15, 2022; 14(9): 1711-1726
Published online Sep 15, 2022. doi: 10.4251/wjgo.v14.i9.1711
Table 1 The clinical characteristics between the two groups

CC group (n = 129)
non-CC group (n = 136)
P value
Gender, n (%)0.177
Male84 (65.1)99 (72.8)
Female45 (34.9)37 (27.2)
Age, yr0.446
mean (SD)57.5 (11.4)58.5 (9.8)
Primary location, n (%)0.812
Up4 (3.1)6 (4.4)
Middle60 (46.5)65 (47.8)
Low65 (50.4)65 (47.8)
Pathology, n (%)0.996
Well differentiated6 (4.7)6 (4.4)
Moderately differentiated95 (73.6)102 (75.0)
Poorly differentiated16 (12.4)16 (11.8)
Others12 (9.3)12 (8.8)
CEA, n (%)0.307
Normal67 (51.9)64 (47.1)
Unnormal49 (38.0)63 (46.3)
Unidentified13 (10.1)9 (6.6)
T stage, n (%)0.650
< T3c49 (38.0)48 (35.3)
> T3b80 (62.0)88 (64.7)
N stage, n (%)0.190
N012 (9.3)7 (5.1)
N+117 (90.7)129 (94.9)
Tumor length (mm)0.916
mean (SD)49.0 (12.7)49.1 (13.7)
Tumor thickness (mm)0.838
mean (SD)16.4 (5.0)16.5 (7.2)
MRF, n (%)0.501
Negative31 (24.0)28 (20.6)
Positive98 (76.0)108 (79.4)
EMVI, n (%)0.565
Negative44 (34.1)51 (37.5)
Positive85 (65.9)85 (62.5)
Numbers of high-risk factor, n (%)0.557
138 (29.5)34 (25.0)
248 (37.2)59 (43.4)
343 (33.3)43 (31.6)
Interval time (d)0.040
mean (SD)71.7 (21.7)76.8 (18.5)
Table 2 The clinical parameters between the two groups after propensity score match and inverse probability of treatment weighting
PSM
IPTW
non-CC group (n = 105)
CC-group (n = 105)
P value
non-CC group (n = 130)
CC-group (n = 135)
P value
Gender, n (%)0.7620.970
Male75 (71.4)73 (69.5)89.4 (68.5)92.6 (68.7)
Female30 (28.6)32 (30.5)41.1 (31.5)42.2 (31.3)
Age0.6920.993
mean (SD)57.7 (11.8)58.3 (9.7)58.2 (11.2)58.2 (9.7)
Primary location, n (%)0.8490.996
Up3 (2.9)2 (1.9)4.9 (3.8)4.9 (3.7)
Middle52 (49.5)50 (47.6)61.0 (46.7)63.8 (47.3)
Low50 (47.6)53 (50.5)64.6 (49.5)66.1 (49.0)
Pathology, n (%)0.9030.999
Well-differentiated5 (4.8)5 (4.8)6.3 (4.9)6.6 (4.9)
Moderately-differentiated79 (75.2)75 (71.4)94.0 (72.0)97.9 (72.6)
Poorly-differentiated12 (11.4)13 (12.4)16.6 (12.7)17.0 (12.6)
Others9 (8.6)12 (11.4)13.6 (10.4)13.3 (9.9)
CEA, n (%)0.4280.997
Normal51 (48.6)58 (55.2)64.1 (49.1)66.8 (49.5)
Unnormal45 (42.9)42 (40.0)55.2 (42.3)56.7 (42.1)
unidentified9 (8.6)5 (4.8)11.2 (8.6)11.3 (8.4)
T stage, n (%)0.5680.992
< T3c41 (39.0)37 (35.2)48.0 (36.8)49.7 (36.9)
> T3b64 (61.0)68 (64.8)82.5 (63.2)85.1 (63.1)
N stage, n (%)0.0970.176
N010 (9.5)4 (3.8)12.1 (9.3)6.7 (5.0)
N+95 (90.5)101 (96.2)118.4 (90.7)128.1 (95.0)
Tumor length (mm)0.9160.983
mean (SD)48.6 (13.0)48.4 (13.2)48.9 (12.5)48.9 (13.5)
Tumor thickness (mm)0.4840.999
mean (SD)16.6 (5.0)16.0 (7.0)16.4 (4.9)16.4 (7.2)
MRF, n (%)> 0.990.865
Negative23 (21.9)23 (21.9)29.7 (22.8)29.5 (21.9)
Positive82 (78.1)82 (78.1)100.7 (77.2)105.3 (78.1)
EMVI, n (%)0.7710.998
Negative35 (33.3)37 (35.2)46.4 (35.6)48.0 (35.6)
Positive70 (66.7)68 (64.8)84.0 (64.4)86.8 (64.4)
Numbers of high-risk factor, n (%)0.5100.883
131 (29.5)26 (24.8)36.5 (28.0)35.1 (26.0)
237 (35.2)45 (42.9)51.2 (39.2)56.9 (42.2)
337 (35.2)34 (32.4)42.8 (32.8)42.8 (31.7)
Interval time (d)0.6590.819
mean (SD)74.4 (20.0)75.6 (18.4)75.5 (25.1)74.8 (17.7)
Table 3 Details of surgical and pathological results in the original samples before matching and after propensity score match in the two groups
Original samples
PSM
non-CC group (n = 124)
CC group (n = 126)
P value
non-CC group (n = 100)
CC group (n = 96)
P value
Interval time (d)0.0150.410
mean (SD)71.7 (21.9)77.9 (18.6)74.5 (20.1)76.8 (18.7)
Surgical method, n (%)0.2320.990
APR42 (33.9)31 (24.6)30 (30.0)29 (30.2)
LAR77 (62.1)91 (72.2)66 (66.0)63 (65.6)
Hartmann5 (4.0)4 (3.2)4 (4.0)4 (4.2)
Surgery time (h)0.6840.953
mean (SD)3.0 (1.3)3.1 (1.4)3.0 (1.3)3.0 (1.4)
Blood loss (mL)0.3450.407
mean (SD)75.4 (51.4)105.4 (145.5)74.5 (47.8)99.3 (105.0)
R0, n (%)123 (99.2)124 (98.4)0.57199 (99.0)94 (97.9)0.537
Numbers of dissected lymph nodes0.1940.502
mean (SD)9.1 (4.9)8.3 (5.0)9 (4.8)8.54 (5.0)
pT satge, n (%)0.4000.136
T021 (16.9)31 (24.6)17 (17.0)28 (29.2)
T16 (4.8)10 (7.0)5 (5.0)9 (9.4)
T241 (33.1)34 (27.0)32 (32.0)28 (29.2)
T354 (43.5)50 (39.7)44 (44.0)30 (31.2)
T42 (1.6)1 (0.8)2 (2.0)1 (1.0)
pN stage, n (%)0.5410.712
N090 (72.6)99 (78.6)72 (72.0)74 (77.1)
N126 (21.0)21 (16.7)22 (22.0)17 (17.7)
N28 (6.5)6 (4.8)6 (6.0)5 (5.2)
TRG, n (%)0.1230.015
021 (16.9)31 (24.6)17 (17.0)28 (29.1)
143 (34.7)51 (40.5)33 (33.0)41 (42.7)
259 (47.6)42 (33.3)49 (49.0)26 (27.1)0.176
31 (0.8)2 (1.6)1 (1.0)1 (1.1)
pT0-2N0, n (%)57 (46.0)66 (52.4)0.31146 (46.0)57 (59.4)0.061
pCR, n (%)18 (14.5)27 (21.4)0.15514 (14.0)24 (25.0)0.051
Table 4 The complete response rate and univariate regression of consolidation chemotherapy in the original samples before matching, after propensity score match and inverse probability of treatment weighting in the two groups
CR
Univariate regression

non-CC group, n (%)
CC group, n (%)
P value
OR (95%CI)
P value
Original samples21 (16.3)33 (24.3)0.1071.648 (0.895-3.033)0.109
PSM17 (16.2)29 (27.6)0.0451.975 (1.008-3.871)0.047
IPTW21 (16.3)35 (25.9)0.0451.185 (1.008-3.395)0.047
Table 5 Toxicities during neoadjuvant treatment in the two groups
non-CC group (n = 129), n (%)
CC group (n = 136), n (%)

Grade 1
Grade 2
Grade 3
Grade 4-5
Grade 1
Grade 2
Grade 3
Grade 4-5
Total59 (45.7)64 (49.6)5 (3.9)066 (48.5)63 (46.3)4 (2.9)0
Leukopenia47 (36.4)29 (22.5)2 (1.6)051 (37.5)27 (19.9)00
Neutropenia22 (17.1)9 (7.0)0022 (16.2)9 (6.6)00
Anemia5 (3.9)6 (4.7)2 (1.6)014 (10.3)5 (3.7)00
Thrombocytopenia9 (7.0)01 (0.8)05 (3.7)000
Aminotransferase increased0 (0.0)1 (0.8)006 (4.4)000
Bilirubin increased19 (14.7)2 (3.1)0018 (13.2)2 (1.5)1 (0.7)0
Nausea39 (30.2)00030 (22.1)1 (0.7)00
Fatigue58 (45.0)3 (2.3)0066 (44.9)2 (1.5)00
Proctitis/diarrhea66 (51.2)36 (27.9)1 (0.8)066 (48.5)39 (28.7)2 (1.5)0
Cystitis38 (29.5)00042 (30.9)000
Radiodermatitis75 (58.1)6 (4.7)0070 (51.5)3 (2.2)00