Abstract 247P
Background
Trastuzumab (H) plus Pertuzumab (P) combined with cytotoxic agents has been the SOC for Her2+BC across perioperative to late stage. Even with high efficacy, optimized treatment strategy still needs to be explored. KN026 is a bispecific monoclonal antibody that targets domain II and IV of HER2. KN026 showed comparable or better efficacy with H+P in preclinical study. The superior efficacy had also been validated in a series of clinical trials in late line Her2+ solid tumors as well as the first-line Her2+ breast cancer and gastric cancer. Here we report the results of KN026 plus docetaxel as neoadjuvant treatment in HER2+ BC pts.
Methods
Treatment naive pts with HER2+ early or LABC were enrolled to receive 4 cycles of KN026 (30mg/kg, ivgtt d1, q3w) and docetaxel (75 mg/m2, ivgtt d1, q3w) as neoadjuvant treatment. The primary endpoint was tpCR rate. Secondary endpoints were bpCR, ORR, safety, etc. This study is registered in ClinicalTrials.gov, number NCT04881929.
Results
From August 9th, 2021, to July 29th, 2022, a total of 30 pts were enrolled from 5 sites. 16 pts (53.3%) were stage II, and 14 pts (46.7%) were stage III; 26 (86.7%) pts with biopsy-confirmed lymph node metastases; 15 (50.0%) pts were hormone receptor positive. As of Nov 21st, 2022, the study completed the primary outcome. 28 pts completed the surgery followed by pathological evaluation, and 2 pts discontinued from the study earlier due to AEs. In FAS, tpCR rate was 56.7% (17/30, 95% CI: 37.43%-74.53%), bpCR rate was 60% (18/30, 95% CI:40.60%-77.34%), ORR was 90.0% (27/30, 95% CI: 73.47%-97.89%). The incidence of TEAEs and CTCAE Grade ≥3 TEAEs were 100% (30/30) and 53.3% (16/30), respectively. The most common (≥5%)Grade ≥3 TEAEs were neutrophil count decreased (50%, 15/30), white blood cell count decreased (40.0%, 12/30), and lymphocyte count decreased (10%, 3/30). 7 (23.3%)pts required docetaxel dose reduction due to AEs. KN026 and docetaxel related SAEs occurred in only one patient. No Grade 5 TEAEs occurred.
Conclusions
KN026 plus docetaxel as neoadjuvant treatment has shown promising clinical benefit and acceptable safety for pts with HER2+ early or LABC. Further validation in a large-scale randomized controlled trial is warranted.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Jiangsu Alphamab Biopharmaceuticals Co. Ltd.
Funding
Jiangsu Alphamab Biopharmaceuticals Co. Ltd.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
233P - Germline genetic testing before formal counseling: Impact in cancer management in a Spanish university hospital
Presenter: Marianela Bringas Beranek
Session: Poster session 02
235TiP - Hamlet.rt Trans: Prospective single-centre translational study evaluating liquid biomarkers of radiation response
Presenter: Mary Denholm
Session: Poster session 02
236TiP - Large-scale prospective observational study to develop a liquid-based detection system of minimal residual disease (MRD): LC-SCRUM-MRD
Presenter: Shingo Kitagawa
Session: Poster session 02
248P - Targeting triple-negative breast cancer metabolism with neoadjuvant chemotherapy plus fasting-mimicking diet plus/minus metformin: The BREAKFAST trial
Presenter: Francesca Ligorio
Session: Poster session 02
250P - The impact of inter-cycle treatment delays on progression-free survival in early stage breast cancer
Presenter: Luke Steventon
Session: Poster session 02
251P - Body mass index as a predictive factor for efficacy of taxane-based chemotherapy in early breast cancer patients
Presenter: Jose Angel García-Sáenz
Session: Poster session 02
252P - Adjuvant chemotherapy in T1a/bN0 breast cancer patients with high oncotype DX recurrence scores (RS>25)
Presenter: Daniela Katz
Session: Poster session 02