The CompassHER2 pCR trial investigates a less intensive neoadjuvant chemotherapy regimen using THP for early-stage HER2-positive breast cancer patients, achieving promising results.
The study enrolled 2,175 patients, with impressive tolerability and low disease progression rates during the 12-week THP regimen.
ER-negative, HER2-positive patients exhibited a remarkable 64% pathologic complete response (pCR) rate, highlighting the regimen's efficacy in this subgroup.
Lower ER expression within ER-positive tumors correlated with higher pCR rates, emphasizing the importance of tumor biology in treatment response.
The combination of trastuzumab and pertuzumab with taxane chemotherapy showed superior pCR rates, with weekly paclitaxel being favored over docetaxel.
Advanced molecular analysis with the HER2DX pCR-score provided predictive biomarkers for treatment personalization, independent of ER status.
Patients achieving pCR after THP could forgo post-surgery chemotherapy, minimizing toxicity while maintaining disease control.
The study's focus on treatment de-escalation and personalized medicine reflects a shift in oncology towards tailored, less toxic therapies.
The long-term impact of the THP regimen on recurrence-free survival is still under evaluation, with implications for future clinical guidelines.
The study's collaborative efforts and clinical implications may influence global cancer treatment strategies, promoting effective yet minimally burdensome care.