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. 2025 Jul 1;13(3):683–694. doi: 10.1007/s40487-025-00353-3

Table 1.

Demographics of three generic groups and the reference group

Characteristics Accord Amarox Sandoz Reference p-value
Total patients 107 81 13 150
Centre (%)
 NKI 0 81 (100) 0 60 (40.0) < 0.01
 LUMC 37 (34.6) 0 0 24 (16.0) < 0.01
 RadboudUMC 49 (45.8) 0 0 41 (27.3) < 0.01
 UMCG 21 (19.6) 0 13 (100) 25 (16.7) < 0.01
Female sex (%) 38 (35.5) 34 (42.0) 6 (46.2) 66 (44.0) 0.56
Median age, years (IQR) 69 (61–75) 70 (59–76) 64 (62–72) 68 (59–75) 0.89
Indication (%)
 Neo-adjuvant 10 (9.3) 21 (25.9) 2 (15.4) 26 (17.3) 0.01
 Adjuvant 25 (23.4) 3 (3.7) 2 (15.4) 14 (9.3) < 0.01
 Palliative 72 (67.3) 57 (70.4) 9 (69.2) 110 (73.3) 0.77
Daily dosea
 < 400 mg 10 (9.3) 10 (12.3) 0 (0) 16 (10.7) 0.70
 400 mg 81 (75.7) 45 (55.6) 12 (92.3) 99 (66.0) 0.01
 > 400 mg 16 (15.0) 26 (32.1) 1 (7.7) 35 (23.3) 0.02
Treatment duration in months (IQR)b 30 (18–71) 33 (19–91) 23 (6–66) 34 (12–81) 0.44
Total AEs before switch (IQR)c 4 (2–6) 4 (3–7) 4 (3–5) 3 (2–6) 0.31

aDosage at date of the switch

bRepresents the median duration of treatment until the switch

cThe median number of imatinib-related adverse events that occurred during full treatment before the switch

NKI Netherlands Cancer Institute, LUMC Leiden University Medical Center, RadboudUMC Radboud University Medical Center, UMCG University Medical Center Groningen, AEs adverse events