Breast
Natalia Polidorio, MD, PhD
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, New York, United States
Natalia Polidorio, MD, PhD
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, New York, United States
Natalia Polidorio, MD, PhD
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, New York, United States
Lauren M. Perry, MD, MAS
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, United States
Varadan Sevilimedu, DrPH
Biostatistics Service, Department of Epidemiology and Biostatistics
Memorial Sloan Kettering Cancer Center, United States
Giacomo Montagna, MD, MPH
Assistant Attending
Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA
New York, New York, United States
Nour Abuhadra, MD
Breast Medicine Service, Division of Solid Tumor Oncology
Memorial Sloan Kettering Cancer Center, United States
Monica Morrow, MD
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Stephanie Downs-Canner, MD
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, United States
George Plitas, MD
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, United States
Pathologic complete response (pCR) rates to neoadjuvant chemotherapy (NAC) in patients with triple-negative breast cancer (TNBC) differ across racial groups, with lower rates for Black patients. The underrepresentation of minority populations in the KN522 trial prompted us to evaluate pCR rates by race in early-stage TNBC patients receiving neoadjuvant chemo-immunotherapy as compared to a pre-KN522 NAC cohort.
Racial distribution for chemo-immunotherapy patients was: 17% Asian, 19% Black, 61% White, and 3% of Other races. In the NAC group, race distribution was 10%, 23%, 61%, and 6% for Asian, Black, White, and Other races, respectively. Clinicopathologic characteristics and pCR rates by race are shown in the table. Overall pCR rates were 36% for patients receiving NAC and 56% for those receiving chemo-immunotherapy. This increase in pCR rate was largely driven by increases in pCR rates for Black patients (29% to 57%) and Asian patients (24% to 60%), with less of a change observed for White (38% to 54%) and no change for Other (63% to 63%) patients. On MVA, after adjusting for factors associated with pCR, such as age, tumor grade, lymphovascular invasion, and nodal disease, Asian patients treated with NAC were less likely to achieve pCR (OR 0.40, 95% CI 0.19-0.81, p = 0.013), and there was a non-significant decrease in pCR in Black patients (OR 0.69, 95% CI 0.42-1.12, p = 0.14). No statistical difference was observed in pCR by race for the chemo-immunotherapy group (p = 0.9), with similar rates between Asian, Black, and White patients (60%, 57%, and 54%, respectively).
Conclusions:
The differences in pCR rates by race in NAC patients were not seen in chemo-immunotherapy patients, with clinically relevant gains in pCR rates for Black and Asian patients. Research focusing on chemo-immunotherapy effects in minority racial groups may guide therapeutic approaches for populations most likely to derive benefit.