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. 2023 Feb 5;14(3):434–445. doi: 10.7150/jca.81588

Table 2.

Side effects of neoadjuvant therapy in the matched cohort

Toxicity Matched NAC (n=413) Full NAC cohort (n=694)
AE N (%)
Yes 378(91.53)
35(8.47)
645(92.94)
No 35(8.47) 49(7.06)
CTCAE grade N (%)
missing 35 49
I 87(23.02) 140(21.71)
II 184(48.68) 329(51.01)
III 81(21.43) 135(20.93)
IV 26(6.88) 41(6.36)
Leukopenia
0 221 319
I 94(48.96) 166(52.04)
II 61(31.77) 96(30.09)
III 27(14.06) 42(13.17)
IV 10(5.21) 15(4.70)
Anaemia
0 135 208
I 199(71.58) 344(70.78)
II 74(26.62) 133(27.37)
III 5(1.80) 9(1.85)
IV 0(0.00) 0(0.00)
Thrombocytopenia
0 80 550
I 53(66.25) 101(70.14)
II 22(27.50) 37(25.69)
III 4(5.00) 5(3.47)
IV 1(1.25) 1(0.69)
Neutropenia
0 265 440
I 52(35.14) 94(37.01)
II 49(33.11) 82(32.28)
III 26(17.57) 42(16.54)
IV 21(14.19) 36(14.17)
Total bilirubin increased
0 125 486
I 95(76.00) 153(73.56)
II 29(23.20) 53(25.48)
III 1(0.80) 2(0.96)
IV 0(0.00) 0(0.00)
Creatinine
0 395 661
I 17(94.44) 30(90.91)
II 1(5.56) 2(6.06)
III 0(0.00) 1(3.03)
IV 0(0.00) 0(0.00)
Emesis
Yes 23(5.57) 51(7.35)
No 390(94.43) 643(92.65)
Diarrhoea
Yes 2(0.48) 2(0.29)
No 411(99.52) 692(99.71)

NAC, neoadjuvant chemotherapy; N, number; AE, adverse effect; CTCAE, Common Terminology Criteria for Adverse Events.