Prospective Study
Copyright ©The Author(s) 2021.
World J Clin Cases. Nov 16, 2021; 9(32): 9869-9877
Published online Nov 16, 2021. doi: 10.12998/wjcc.v9.i32.9869
Table 1 Comparison of general information of the patients between the two groups
Group
n
Gender(n)
Age (yr)
Colorectal cancer
Male
Female
Max
Min
mean ± SD
Colon cancer
Rectal caner
Experimental352114674052.24 ± 13.20287
Control332211684255.63 ± 12.39258
Table 2 Hand-foot skin reactions (National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0)
Grade
Item description
0No clinical manifestations
1Have red or discolored skin or painless dermatitis
2Show changes in skin (such as peeling, bleeding, and swollen) or have blisters or sores, without any dysfunction
3Show changes in skin due to dysfunctions caused by ulcerative dermatitis or pain
Table 3 Gastrointestinal reactions (National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0)
Grade
Item description
0No clinical manifestations
1Lack of appetite, without any change in eating habits
2Less food intake, no significant weight loss or malnutrition, have signs of intravenous fluid replacement for < 24 h
3Less energy and water intake, have signs of intravenous fluid rehydration, tube feeding and parenteral nutrition ≥ 24 h
Table 4 Comparisons of scores of traditional Chinese medicine symptoms between the two groups (mean ± SD points)
Group
n
Poor appetite
Abdominal distention
Loose stool
Fatigue
Emaciation
Experimental351.11 ± 0.760a1.40 ± 0.728a1.37 ± 0.209a1.37 ± 0.501a1.54 ± 0.625a
Control332.75 ± 0.7412.21 ± 0.7532.64 ± 0.5212.24 ± 1.1222.15 ± 0.917
Table 5 Comparison of Karnofsky performance scale scores between the two groups (mean ± SD points)
Group
n
Before the treatments
After the treatments
Experimental3579.17 ± 4.12588.51 ± 6.773a,d
Control3378.75 ± 3.47581.44 ± 4.539a
Table 6 Comparison of serum levels of T-cell subsets between groups before and after the treatments (mean ± SD)
Group
n
Time
CD3+ (%)
CD4+ (%)
CD4+/CD8 (%)
CD8+ (%)
Experimental35Before treatment41.52 ± 5.2132.07 ± 3.310.51 ± 0.1552.25 ± 5.37
After treatment62.3 ± 5.53a,d43.4 ± 4.99a,d1.02 ± 0.29a,d40.52 ± 4.58a,d
Control33Before treatment 42.52 ± 4.5831.15 ± 3.250.55 ± 0.1352.12 ± 6.59
After treatment53.25 ± .6.62a37.72 ± 4.56a0.77 ± 0.15a48.46 ± 5.58a
Table 7 Comparison of grades of nausea between the two groups
Group
n
Grade
0
1
2
3
Experimental35121571
Control3347166
Table 8 Grades of hand-foot skin reactions between the two groups
Group
n
Grade
0
1
2
3
Experimental351013111
Control3338193
Table 9 Adverse effects between the two groups, n (%)
Group
n
Myelosuppression
Liver dysfunction
Renal dysfunction
Coagulation disorder
ECG abnormality
Experimental358 (22.8)7 (20.0)1 (2.8)3 (8.5)3 (8.5)
Control336 (18.1)5 (15.1)2 (6.0)3 (9.1)2 (6.1)