Table 2.
Preoperative chemotherapy (n = 45) | Postoperative chemotherapy (n = 31) | |||||
---|---|---|---|---|---|---|
Any grade | ≥ Grade 3 | Step 1 (n = 11) | Step 2 (n = 20) | |||
Any grade | ≥ Grade 3 | Any grade | ≥ Grade 3 | |||
Hematological | ||||||
Platelet count decreased | 17 (37.8) | 0 (0.0) | 1 (9.1) | 0 (0.0) | 9 (45.0) | 1 (5.0) |
Anaemia | 7 (15.6) | 1 (2.2) | 1 (9.1) | 0 (0.0) | 2(10.0) | 1 (5.0) |
Neutrophil count decreased | 6 (13.3) | 4 (8.9) | 3 (27.3) | 1 (9.1) | 6 (30.0) | 2 (10.0) |
WBC count decreased | 4 (8.9) | 1 (2.2) | 2 (18.2) | 0 (0.0) | 3 (15.0) | 0 (0.0) |
Non-hematological | ||||||
Peripheral sensory neuropathy | 32 (71.1) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 9 (45.0) | 0 (0.0) |
Diarrhoea | 27 (60.0) | 8 (17.8) | 4 (36.4) | 1 (9.1) | 12 (60.0) | 0 (0.0) |
Nausea | 25 (55.6) | 1 (2.2) | 2 (18.2) | 0 (0.0) | 9 (45.0) | 0 (0.0) |
Decreased appetite | 20 (44.4) | 2 (4.4) | 5 (45.5) | 1 (9.1) | 10 (50.0) | 1 (5.0) |
Stomatitis | 20 (44.4) | 2 (4.4) | 1 (9.1) | 0 (0.0) | 4 (20.0) | 0 (0.0) |
Constipation | 20 (44.4) | 0 (0.0) | 1 (9.1) | 0 (0.0) | 1 (5.0) | 0 (0.0) |
AST increased | 13 (28.9) | 0 (0.0) | 2 (18.2) | 0 (0.0) | 6 (30.0) | 0 (0.0) |
ALT increased | 12 (26.7) | 0 (0.0) | 2 (18.2) | 0 (0.0) | 5 (25.0) | 0 (0.0) |
Fatigue | 9 (20.0) | 1 (2.2) | 2 (18.2) | 0 (0.0) | 2 (10.0) | 0 (0.0) |
Pyrexia | 9 (20.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 2 (10.0) | 0 (0.0) |
Duodenal perforation | 1 (2.2) | 1 (2.2) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
Hypokalaemia | 1 (2.2) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 4 (20.0) | 3 (15.0) |
Palmar-plantar erythrodysaesthesia syndrome | 0 (0.0) | 0 (0.0) | 4 (36.4) | 0 (0.0) | 1 (5.0) | 0 (0.0) |
Data are n (%). Adverse events that commonly occur are shown. Adverse events were graded according to the Common Terminology Criteria for Adverse Events (version 4.03)
WBC white blood cell, AST aspartate aminotransferase, ALT alanine aminotransferase