Impact of diabetes and glycemic control on pathologic complete response after neoadjuvant chemotherapy in breast cancer in an Afro-Caribbean population: A retrospective cohort study.

R Rachelle Hamadi (SUNY Downstate Health Sciences University, New York, NY) Z Zakaria Alameddine (SUNY Downstate Medical Center College of Medicine, Brooklyn, NY) I Imad Karam (2SUNY Downstate Health Sciences University, Brooklyn, United States) C Cassandre Salib (SUNY Downstate, Brooklyn, NY) S Sunydip Gill (SUNY Downstate Medical Center, Brooklyn, NY) Y Yanming Wu (SUNY Downstate Health Sciences University, Brooklyn, NY) J Joshua Salama (SUNY Downstate Medical Center, Brooklyn, NY) J Jordonna Brown (SUNY Downstate Medical Center, Brooklyn, NY)

Abstract

e12625 Background: Diabetes mellitus and hyperglycemia may adversely affect cancer outcomes and response to systemic therapy in breast cancer (Peairs et al., 2010; Srokowski et al., 2009). Pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) is a validated surrogate marker of improved long-term outcomes (Spring et al., 2020; van Mackelenbergh et al., 2023). This study evaluated whether diabetes and baseline HbA1c are associated with pCR in breast cancer patients receiving NACT. Methods: We conducted a retrospective cohort study of breast cancer patients treated with NACT at a single institution. Included patients had a documented neoadjuvant chemotherapy regimen, known pCR status, and known diabetes status, defined as HbA1c ≥ 6.5. The primary outcome was pCR (yes/no). The main exposures were diabetes (yes/no) and HbA1c at diagnosis. Categorical variables were compared using Fisher’s exact test, and continuous variables using Welch’s t-test; multivariable logistic regression was used to estimate adjusted odds ratios (ORs) for pCR, including diabetes, age, BMI, and HbA1c. Results: Of 153 patients who received NACT, 52 had complete data for diabetes and pCR and were included in the primary analysis. Among these, 40 (76.9%) had diabetes and 12 (23.1%) did not have diabetes; 30 (57.7%) achieved pCR. pCR occurred in 75.0% of patients without diabetes versus 52.5% of patients with diabetes (Fisher’s exact OR = 0.37; p = .20). Baseline HbA1c was higher in patients without pCR than in those with pCR (mean 8.05% vs. 7.19%; p = .22). In multivariable logistic regression, diabetes was not an independent predictor of pCR (adjusted OR = 0.33; 95% CI [0.03, 4.31]). Age, BMI, and HbA1c were also not significantly associated with pCR. Conclusions: In this cohort, diabetes status and baseline HbA1c were not significantly associated with pCR after NACT, although both diabetes and higher HbA1c showed non-significant trends toward lower pCR rates. Larger, adequately powered studies are needed to clarify the impact of diabetes and glycemic control on neoadjuvant treatment response in breast cancer.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (8)

R

Rachelle Hamadi

SUNY Downstate Health Sciences University, New York, NY

Z

Zakaria Alameddine

SUNY Downstate Medical Center College of Medicine, Brooklyn, NY

I

Imad Karam

2SUNY Downstate Health Sciences University, Brooklyn, United States

C

Cassandre Salib

SUNY Downstate, Brooklyn, NY

S

Sunydip Gill

SUNY Downstate Medical Center, Brooklyn, NY

Y

Yanming Wu

SUNY Downstate Health Sciences University, Brooklyn, NY

J

Joshua Salama

SUNY Downstate Medical Center, Brooklyn, NY

J

Jordonna Brown

SUNY Downstate Medical Center, Brooklyn, NY