Copyright: ©Author(s) 2026.
World J Gastroenterol. Apr 21, 2026; 32(15): 116121
Published online Apr 21, 2026. doi: 10.3748/wjg.v32.i15.116121
Published online Apr 21, 2026. doi: 10.3748/wjg.v32.i15.116121
Table 1 Common toxicities of first-line colorectal cancer chemotherapy regimens that warrant integrated prediction
| Toxicity type | Occurrence of risk | Clinical impact | Associated regimens | Impact on decision-making |
| Chemotherapy-induced myelosuppression | High (FOLFOX); low (CAPOX) | Neutropenia, anemia, thrombocytopenia; risk of fever, infection, fatigue, bleeding | FOLFOX, FOLFIRI, CAPOX | Common reasons for dose delay, reduction, or use of growth factor support |
| Severe diarrhea | High (FOLFOX); medium (CAPOX) | Watery stools, dehydration, and electrolyte imbalance | FOLFOX, FOLFIRI, CAPOX | Frequent cause of dose modification or treatment interruption; requires proactive management |
| Peripheral neuropathy | Low (FOLFOX); high (CAPOX) | Numbness, tingling in the limbs, can progress to functional impairment (e.g., difficulty with fine motor tasks) | FOLFOX, CAPOX | Cumulative toxicity often leads to dose reduction or discontinuation of oxaliplatin |
| Hand-foot syndrome | Medium (FOLFOX); high (CAPOX) | Erythema, swelling, pain, blistering on palms and soles | FOLFOX, CAPOX | May necessitate dose reduction or interruption of capecitabine/fluorouracil |
- Citation: Qin YW, Li PW, Liang XY, Mo Y, Chen DW. Letter to the Editor: Balancing efficacy and toxicity: The critical role of predictive models in colorectal cancer chemotherapy. World J Gastroenterol 2026; 32(15): 116121
- URL: https://www.wjgnet.com/1007-9327/full/v32/i15/116121.htm
- DOI: https://dx.doi.org/10.3748/wjg.v32.i15.116121
