Posted: Thursday, December 19, 2024
Investigators comparing the neoadjuvant combination of paclitaxel, margetuximab-cmkb, and pertuzumab (TMP) with paclitaxel, trastuzumab, and pertuzumab (THP) in patients with newly diagnosed stage II to III HER2-positive early breast cancer and a CD16A FF/FV genotype found no statistically significant improvement in pathologic complete response rate. Safety and tolerability were also similar between the two regimens, noted Adrienne Waks, MD, of Dana-Farber Cancer Institute, Boston, and colleagues in their work, presented during the 2024 San Antonio Breast Cancer Symposium (SABCS; Abstract LB1-02).
Between 2020 and 2024, the 171 female patients (median age, 53 years) were randomly assigned on a 2:1 basis to neoadjuvant TMP or THP for four cycles. In this trial, patients could have any hormone receptor (HR) status and CD16A genotype FF or FV by central testing; estrogen receptor status and baseline clinical stage were stratification factors. In all, 65% of patients had HR-positive tumors, 87% had cT1–T2 tumors, and 35% had clinically node-positive disease. Additionally, 77% were White, 10% were Black, and 4% were Asian; 13% were Hispanic. The pathologic complete response rate in the TMP arm was 56%, vs 46% in the THP arm (P = .25).
Here are the key study results:
Disclosure: For full disclosures of the study authors, visit sabcs.org.
2024 San Antonio Breast Cancer Symposium