Abstract PS2-07-06: Prevalence and dynamics of circulating tumor DNA among patients with triple-negative breast cancer undergoing preoperative systemic therapy with or without immunotherapy

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Authors: T. R. Yoo, Stefania Morganti, Qingchun Jin, A. Patel, Craig Snow, Katheryn Santos, Catherine Stever, Olivia Cunningham, Tasnim Rahman, J. Tejeda-Zanudo, Joanna Bagińska, Jad Bsat
+27 more Moli Luo, I. G. Martino, B. M. Drummey, S. A. Virani, K. Howarth, C. Rushton, S. Birkeälv, S. Woodhouse, G. Putcha, E. Christoforou, Sophie A. Kirschner, A. Moeini, N. Ahmad, N. M. Tung, Natalie Faye Sinclair, Maria A. Constantinou, M. Faggen, Sara Sinclair, SS Lo, J. L. Meisel, E. P. Winer, E. A. Mittendorf, Nabihah Tayob, U. N. Lin, S. M. Tolaney, A. C. Garrido-Castro, H. A. Parsons
Cited by: 1

Abstract

Abstract Background: Preoperative systemic therapy (PST) with immunotherapy (IO) is the current standard-of-care for patients (pts) with early-stage triple-negative breast cancer (TNBC). Circulating tumor DNA (ctDNA) persistence in the (neo)adjuvant setting is associated with residual disease at surgery and a higher risk of recurrence. However, studies of ctDNA in TNBC have not evaluated treatment in the modern, IO-containing era. We tested the performance of a highly sensitive assay to evaluate the prevalence and dynamics of ctDNA in the neoadjuvant TNBC setting with and without IO. Methods: We prospectively enrolled and retrospectively identified patients with TNBC receiving PST in an IRB-approved, multi-center registry. Plasma samples were collected at diagnosis (baseline), 4-7 weeks after start of PST (on-treatment), at completion of PST and before surgery (preop), within 3 months after surgery (postop), and every 6 months during follow-up. ctDNA was measured using the Pathlight assay (SAGA Dx), a tumor-informed assay based on structural variants identified from 15X whole-genome sequencing of tumor/normal samples, to detect and quantify minimal residual disease. The primary endpoint was ctDNA detection rate during and after PST. Results: We evaluated 444 plasma samples from 80/97 (82.5%) pts with >1 plasma sample, sufficient tumor tissue and available buffy coat. Pts were a median of 50.4 years old, and 34 (42.5%) had stage III disease. Pts were enrolled between 2019 and 2024, and due to a change in standard treatment, 31 (38.8%) pts received cytotoxic chemotherapy (CT) alone, while 49 (61.2%) pts received an IO-containing regimen. At the time of surgery, 49 (61.3%) pts had pathologic complete response (pCR). Personalized ctDNA assays were designed targeting 5-16 structural variants (median 12). ctDNA was detected at baseline in 71/76 (93.4%; 95% CI 85.3 - 97.8) pts, on-treatment in 24/70 (34.3%; 95% CI 23.3-46.6) pts, preop in 7/53 (13.2%; 95% CI 5.5-25.3) pts, and postop in 8/59 (13.6%; 95% CI 6.0-25.0) pts. Among pts who were ctDNA-positive (ctDNA+) at baseline with a paired on-treatment sample (n = 62), 37 (59.7%) pts cleared ctDNA by the on-treatment timepoint. All pts who cleared on-treatment remained ctDNA-negative at the preop timepoint, when available (n = 26). Among pts who were ctDNA+ at baseline with a paired preop sample (n = 46), 39 (84.8%) pts cleared ctDNA at completion of PST. The negative predictive value (NPV) of ctDNA clearance for pCR by the on-treatment timepoint was 78.4% (29/37; 95% CI 61.8-90.2), while the NPV at the preop timepoint was 71.8% (28/39; 95% CI 55.1-85.0). On IO- vs non-IO containing regimens, the NPV of ctDNA clearance at the on-treatment timepoint was 85.7% (18/21; 95% CI 63.7-97.0) for IO-containing regimens and 68.8% (11/16; 95% CI 41.3-89.0) for pts undergoing cytotoxic CT alone. Among pts with residual disease at surgery (n = 31), 19 (61.3 %) underwent adjuvant therapy including IO. 6/19 pts remained ctDNA+ after surgery, with persistent ctDNA in all subsequent samples until clinical recurrence. Median postoperative follow-up was 26.2 (IQR 18.6, 37.3) months. Of 8 pts who remained ctDNA+ after surgery, 7 (87.5%) had a clinical recurrence with a median lead time of 10.9 (IQR 6.1, 16.4) months. All (n = 10) pts experiencing distant recurrence were ctDNA+ prior to the event. Follow-up is ongoing. Conclusions: ctDNA detection rate was high among pts with TNBC receiving PST. In pts with residual disease, ctDNA detected after surgery persisted despite adjuvant therapy; all such pts developed disease recurrence. This study highlights ctDNA as a promising biomarker for personalized risk assessment and systemic treatment guidance in pts with early-stage TNBC receiving modern preoperative systemic therapy. Citation Format: T. R. Yoo, S. Morganti, Q. Jin, A. Patel, C. Snow, K. Santos, C. Stever, O. Cunningham, T. Rahman, J. Tejeda-Zanudo, J. Baginska, J. Bsat, M. Luo, I. G. Martino, B. M. Drummey, S. A. Virani, K. Howarth, C. Rushton, S. Birkeälv, S. Woodhouse, G. Putcha, E. Christoforou, S. Kirschner, A. Moeini, N. Ahmad, N. Tung, N. Sinclair, M. Constantinou, M. R. Faggen, S. Sinclair, S. Lo, J. L. Meisel, E. Winer, E. A. Mittendorf, N. Tayob, U. N. Lin, S. M. Tolaney, A. Garrido-Castro, H. A. Parsons. Prevalence and dynamics of circulating tumor DNA among patients with triple-negative breast cancer undergoing preoperative systemic therapy with or without immunotherapy [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS2-07-06.

Fields of Study & Subjects

Cancer Genomics and Diagnostics Single-cell and spatial transcriptomics Advanced biosensing and bioanalysis techniques

Publication details

Journal / source
Clinical Cancer Research
Publisher
American Association for Cancer Research (AACR)
Volume
32
Issue
4_Supplement
Pages
PS2–07
Publication date
17 February 2026
Language
EN