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©The Author(s) 2025.
World J Gastrointest Oncol. Jan 15, 2025; 17(1): 96822
Published online Jan 15, 2025. doi: 10.4251/wjgo.v17.i1.96822
Published online Jan 15, 2025. doi: 10.4251/wjgo.v17.i1.96822
Feature | TOSCA trial[20] | TRIBE trial[21] | IRCCS Pascale[22] |
Setting | Colon cancer high-risk stage 2 or stage 3 | Colo-rectal cancer stage 4 | Gastrointestinal malignancies |
Treatment | FOLFOX/CAPOX | FOLFOXIRI/FOLFIRI + bevacizumab | Patients candidates for fluoropyrimidines |
Patients | 508 | 439 | 1000 |
Total number of tested variants | 10 | 3 | 5 |
Prevalence of the four recommended variants in heterozygosity | 19/508 (3.7) | 10/439 (2.3)1 | 39/1000 (3.9) |
Prevalence of the four recommended variants + DPYD6 in heterozygosity | 84/508 (16.5) | 0/439 (0)2 | 180/1000 (18) |
Prevalence of the four recommended variants + DPYD6 in homozygosity | 5/508 (1.0)3 | 0/439 (0)2 | 5/1000 (0.5)3 |
- Citation: D'Amato M, Iengo G, Massa N, Carlomagno C. Dihydropyrimidine dehydrogenase polymorphisms in patients with gastrointestinal malignancies and their impact on fluoropyrimidine tolerability: Experience from a single Italian institution. World J Gastrointest Oncol 2025; 17(1): 96822
- URL: https://www.wjgnet.com/1948-5204/full/v17/i1/96822.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v17.i1.96822