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. 2023 Nov 23;15(23):5547. doi: 10.3390/cancers15235547

Table 2.

Incidence of adverse effects in the induction phase in 492 patients studied for whom toxicity data were available at this stage of treatment. Panel A shows the data for the SR group; Panel B for the ImR group. Bolds are used to indicate significant values.

Panel A PEG − DNR+ PEG + DNR+ PEG + DNR− p
n % n % n %
Total number of patients 101 100 99 100 83 100
Amylase (>2–5 × UNL) 0 0 2 2.0 2 2.4 0.317
Fibrinogen (>40% reduction) 3 3.0 13 13.1 11 13.3 0.020
Thrombosis (deep vein thrombosis, need AC therapy or embolism) 2 2.0 1 1.0 1 1.2 0.829
Hyperglycemia (>13.9 mmole/L) 1 1.0 2 2.0 1 1.2 0.812
Infection 58 57.4 57 57.6 52 62.6 0.725
Panel B PEG− PEG+ p
n % n %
Total number of patients 111 100 98 100
Amylase (>2–5 × UNL) 1 0.9 3 3.1 0.255
Fibrinogen (>40% reduction) 10 9.0 12 12.2 0.447
Thrombosis (deep vein thrombosis, need AC therapy or embolism) 1 0.9 1 1.0 0.929
Hyperglycemia (>13.9 mmole/L) 3 2.7 7 7.1 0.133
Infection 69 62.2 66 67.3 0.434

UNL—upper normal limit; AC—anticoagulant.