
DESTINY-Gastric04 Trial of T-DXd Shows OS Benefit in HER2+ Gastric Cancer
Arturo Loaiza-Bonilla, MD, MSEd, explains the background and findings of the phase 3 DESTINY-Gastric04 trial.
Arturo Loaiza-Bonilla, MD, MSEd, systemwide chief of hematology and oncology at St. Lukes University Health Network and co-founder and chief medical officer at Massive Bio, explains the background and findings of the phase 3 DESTINY-Gastric04 trial (NCT04704934).
The DESTINY-Gastric04 trial demonstrated that fam-trastuzumab deruxtecan-nxki (T-DXd; Enhertu) significantly improves overall survival (OS) compared with ramucirumab (Cyramza) plus paclitaxel in patients with HER2-positive unresectable or metastatic gastric cancer (GC) or gastroesophageal junction adenocarcinoma (GEJ) after prior trastuzumab therapy. Presented at the
Progression-free survival was improved with T-DXd (6.7 months vs 5.6 months; HR 0.74; P = .0074), along with higher 6- and 12-month PFS rates. The confirmed overall response rate was significantly greater with T-DXd at 44.3% compared to 29.1%, with longer duration of response (7.4 vs 5.3 months). Disease control rate was 91.9% with T-DXd, including complete responses in 3% of patients, compared to 75.9% with ramucirumab plus paclitaxel.
The trial enrolled 494 patients globally, randomized 1:1 to receive either T-DXd every three weeks or ramucirumab plus paclitaxel on a 28-day cycle. Eligible patients had HER2-positive disease confirmed post-progression on trastuzumab and no active central nervous system metastases. Key exclusion criteria included interstitial lung disease or pneumonitis.
Safety profiles showed treatment-emergent adverse events (TEAEs) of any grade in over 90% of patients in both arms. Grade 3 or higher neutropenia was most common. Interstitial lung disease/pneumonitis occurred in 13.9% of T-DXd patients versus 1.3% in the comparator group. TEAEs led to dose modifications and discontinuations in both groups.






































