Impact of antiemetic prophylaxis on reducing trastuzumab deruxtecan dose modifications in HER2+/HER2-low breast cancer.
[BACKGROUND] Avoiding unnecessary dose reductions is important for patients with advanced breast cancer (ABC) receiving trastuzumab deruxtecan (T-DXd).
- p-value P = 0.033
- p-value P = 0.001
APA
Shin J, Kim JY, et al. (2026). Impact of antiemetic prophylaxis on reducing trastuzumab deruxtecan dose modifications in HER2+/HER2-low breast cancer.. Future oncology (London, England), 22(3), 321-326. https://doi.org/10.1080/14796694.2026.2617853
MLA
Shin J, et al.. "Impact of antiemetic prophylaxis on reducing trastuzumab deruxtecan dose modifications in HER2+/HER2-low breast cancer.." Future oncology (London, England), vol. 22, no. 3, 2026, pp. 321-326.
PMID
41552955
Abstract
[BACKGROUND] Avoiding unnecessary dose reductions is important for patients with advanced breast cancer (ABC) receiving trastuzumab deruxtecan (T-DXd). Nausea and vomiting, the most common adverse events of T-DXd, frequently necessitate dose reductions, which may impact treatment benefit.
[METHODS] This retrospective exploratory study investigated the impact of triple antiemetic regimen (TAR) prophylaxis on T-DXd dose preservation over time. Data from 143 human epidermal growth factor receptor 2 (HER2)-positive or HER2-low ABC patients who received ≥2 T-DXd cycles were stratified based on TAR use in the first cycle. TAR included an NK receptor antagonist, a 5-HT receptor antagonist (or fixed netupitant/palonosetron combination), and dexamethasone.
[RESULTS] Patients receiving TAR in the first cycle were significantly less likely to require T-DXd dose reductions in subsequent cycles than the non-TAR group (31.3% vs. 66.7%, P = 0.033). The lowest T-DXd dose relative to initial dose for each patient was significantly higher in the TAR group than in the non-TAR group (100% vs. 80.6%, P = 0.001). There was a trend toward a longer median time to T-DXd dose reduction in the TAR group (15.7 vs. 3.9 months; P = 0.183).
[CONCLUSION] These findings suggest that upfront TAR may help maintain the dosing of T-DXd in patients with HER2-positive or HER2-low ABC.
[METHODS] This retrospective exploratory study investigated the impact of triple antiemetic regimen (TAR) prophylaxis on T-DXd dose preservation over time. Data from 143 human epidermal growth factor receptor 2 (HER2)-positive or HER2-low ABC patients who received ≥2 T-DXd cycles were stratified based on TAR use in the first cycle. TAR included an NK receptor antagonist, a 5-HT receptor antagonist (or fixed netupitant/palonosetron combination), and dexamethasone.
[RESULTS] Patients receiving TAR in the first cycle were significantly less likely to require T-DXd dose reductions in subsequent cycles than the non-TAR group (31.3% vs. 66.7%, P = 0.033). The lowest T-DXd dose relative to initial dose for each patient was significantly higher in the TAR group than in the non-TAR group (100% vs. 80.6%, P = 0.001). There was a trend toward a longer median time to T-DXd dose reduction in the TAR group (15.7 vs. 3.9 months; P = 0.183).
[CONCLUSION] These findings suggest that upfront TAR may help maintain the dosing of T-DXd in patients with HER2-positive or HER2-low ABC.
MeSH Terms
Humans; Female; Breast Neoplasms; Trastuzumab; Erb-b2 Receptor Tyrosine Kinases; Retrospective Studies; Middle Aged; Antiemetics; Vomiting; Nausea; Adult; Aged; Immunoconjugates; Antineoplastic Combined Chemotherapy Protocols; Dexamethasone; Palonosetron; Camptothecin; Piperazines; Pyridines; Benzeneacetamides
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