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

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.

Authors

Institutions

Publication Details

Journal
Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps2-07-06
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Moli Luo, Qingchun Jin, Jad Bsat, Natalie Sinclair et al.
Clinical Cancer Research
Cancer Genomics and Diagnostics
article

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

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

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.

Clinical Cancer ResearchVol. 32(4_Supplement)
AstraZeneca (United Kingdom) (GB), Brigham and Women's Hospital (US), Beth Israel Deaconess Medical Center (US), Emory University (US), Rhode Island Hospital (US), Asan Medical Center (KR), Stamford Hospital (US), Yale Cancer Center (US), Eastern Maine Medical Center (US), AstraZeneca (Singapore) (SG), Dana-Farber Cancer Institute (US), Advanced Animal Diagnostics (United States) (US), AstraZeneca (Spain) (ES), Berkshire Health Systems (US)
Good health and well-being
Openalex Percentile: Top 53%
Cancer Genomics and Diagnostics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.