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Retrospective Cohort Study
©The Author(s) 2025.
World J Gastroenterol. Nov 14, 2025; 31(42): 110069
Published online Nov 14, 2025. doi: 10.3748/wjg.v31.i42.110069
Table 2 Grade 3/4 adverse events and adherence/feasibility of each treatment group (n = 63), n (%)

Conventional (n = 42)
Early (n = 21)
P value
RDI (%), mean ± SD68.58 ± 27.6465.34 ± 28.070.587
Median (IQR)73.4 (51.88, 96.25)67.50 (46.38, 95)
Completion rate
4 cycles34 (81.0)17 (81.0)1.000
8 cycles16 (38.1)7 (33.3)0.786
Dose down rate0.026
None31 (73.8)9 (42.9)
Reduction11 (26.2)12 (57.1)
Schedule change rates0.08
None26 (61.9)18 (85.7)
Change16 (38.1)3 (14.3)
Adverse event
Overall toxicity18 (42.9)12 (57.1)0.285
Related death00NA
Leukopenia4 (9.5)1 (4.8)0.657
Neutropenia15 (35.7)10 (47.6)0.363
Thrombocytopenia8 (19.0)3 (14.0)0.639
Anorexia12 (28.6)9 (42.9)0.257
Vomiting10 (24.4)4 (19.0)0.085
Neurotoxicity1 (2.4)2 (9.5)0.219
Diarrhea3 (7.1)2 (9.5)0.742


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