Abstract PS2-09-25: Monitoring Upregulation of PD-L1 in Cancer Associated Macrophage-Like Cells in Blood Predicts Clinical Outcomes in Metastatic Cancer Patients Treated with PD-L1 Immunotherapies

Abstract Background Numerous studies have shown the efficacy of PD-L1/PD-1 based immunotherapies (IMT) for treating patients with metastatic Breast Cancer (MBC) when there is high expression of PD-L1 in their tumor cells and/or tumor immune cells. However, many patients with high PD-L1 tumors do not respond to IMT, and some patients with negative/low PD-L1 tumors may respond to IMTs. The poor correlations between IHC scores and IMT responses are often attributed to the dynamic nature of PD-L1 which may upregulate after chemotherapy, radiation, or other systemic therapies, which is not quantified by IHC tumor immunostaining. Recently, a number of clinical trials have described PD-L1 upregulation in giant phagocytic stromal macrophages found in circulation, i.e. Cancer associated macrophage-like cells (CAML), that may correlate with IMT responses in solid tumors. We conducted a prospective pilot study to monitor the peripheral blood of n=67 MBC patients undergoing systemic treatment with IMT in combination with other therapies, to evaluate CAML PD-L1 prior to and post IMT induction (∼47 days) with clinical outcome analysis at 2 years. Methods In a prospective pilot study of previously treated MBC patients n=67, all starting new lines of systemic therapy in combination with IMT (pembrolizumab [n=57], nivolumab [n=2], or atezolizumab [n=8]) with active progressive metastatic disease. Of the patients, median age was 58.2 (range: 32-73). Median prior lines of therapy in the metastatic setting was 2 (range 0-14). Race demographics (Caucasian=43, Black=7, Hispanic=4, Asian=3 & unknown/other=11). ECOG 0 (n=34) and ECOG 1 (n=33). Visceral metastasis (n=43) and non-visceral (n=24). ER positivity was 37% (n=25), PR positivity was 39% (n=26), HER2 positivity was 13% (n=9) and 52% were triple negative breast cancer (n=35). Histology was IDC (n=52), Other (n=11), ILC (n=2), & IBC (n=2). We isolated CAMLs from 7.5 ml baseline (T0) blood using the LifeTracDx® PD-L1 test and scored PD-L1 as high or low. If possible, a follow-up sample (T1) was taken (∼47 days) after IMT induction. Patient’s progressive free survival (PFS) and overall survival (OS) hazard ratios (HRs) were analyzed by censored univariate analysis based on RECIST v1.1 over 2 years. Results Baseline T0 PD-L1 CAML data was available for 94% (n=63/67) of patients, with 44% (n=28/63) having high CAML PD-L1 which was not correlated with improved PFS (HR=1.3, 95%CI=0.7-2.3, p=0.5376) or OS (HR=1.3, 95%CI=0.7-2.5, p=0.5915). T1 PD-L1 CAML data was available for 78% (n=52/67) of patients, with 58% (n=30/52) having high CAML PD-L1 which significantly correlated with improved PFS (HR=3.1, 95%CI=1.3-7.2 p=0.0170,) and improved OS (HR=4.2, 95%CI=1.6-11.4, p=0.0102). In comparing CAML PD-L1 change post IMT, it was found that consistently low PD-L1 at T0 & T1 had the poorest responses, median PFS (mPFS)=2.2 months and median OS (mOS)=7.2 months. In contrast, patients who increased CAML PD-L1 after IMT induction had better responses, mPFS=6.3 months and mOS=13.1 months. Further, patients with consistently high PD-L1 at T0 & T1 had the best response rates, mPFS=9.5 months and mOS=19.7 months. Conclusion Here we describe a blood-based biopsy which can monitor dynamic PD-L1 changes in circulating tumor immune cells and may predict enhanced clinical benefit to PD-L1 IMTs in MBC. While an initial pilot study on a small population of patients, PD-L1 expression on CAMLs appears to identify patients with improved IMT responses and suggests larger validation studies are needed. Citation Format: D. L. Adams, M. Cristofanilli, C. Reduzzi, W. V. Williams, G. Del Priore, S. Chumsri, T. Iwase, N. T. Ueno, A. B. Duffy, C. Tang. Monitoring Upregulation of PD-L1 in Cancer Associated Macrophage-Like Cells in Blood Predicts Clinical Outcomes in Metastatic Cancer Patients Treated with PD-L1 Immunotherapies [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 PS2-09-25.

Authors

Institutions

Publication Details

Journal
Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps2-09-25
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract PS2-09-25: Monitoring Upregulation of PD-L1 in Cancer Associated Macrophage-Like Cells in Blood Predicts Clinical Outcomes in Metastatic Cancer Patients Treated with PD-L1 Immunotherapies

C. Tang, T. Iwase, C. Reduzzi, D. L. Adams et al.
Clinical Cancer Research
Immune cells in cancer
article

Abstract PS2-09-25: Monitoring Upregulation of PD-L1 in Cancer Associated Macrophage-Like Cells in Blood Predicts Clinical Outcomes in Metastatic Cancer Patients Treated with PD-L1 Immunotherapies

C. Tang, T. Iwase, C. Reduzzi, D. L. Adams, S. Chumsri, N. T. Ueno, A. B. Duffy, M. Cristofanilli, W. V. Williams, G. Del Priore
article en

Abstract

Abstract Background Numerous studies have shown the efficacy of PD-L1/PD-1 based immunotherapies (IMT) for treating patients with metastatic Breast Cancer (MBC) when there is high expression of PD-L1 in their tumor cells and/or tumor immune cells. However, many patients with high PD-L1 tumors do not respond to IMT, and some patients with negative/low PD-L1 tumors may respond to IMTs. The poor correlations between IHC scores and IMT responses are often attributed to the dynamic nature of PD-L1 which may upregulate after chemotherapy, radiation, or other systemic therapies, which is not quantified by IHC tumor immunostaining. Recently, a number of clinical trials have described PD-L1 upregulation in giant phagocytic stromal macrophages found in circulation, i.e. Cancer associated macrophage-like cells (CAML), that may correlate with IMT responses in solid tumors. We conducted a prospective pilot study to monitor the peripheral blood of n=67 MBC patients undergoing systemic treatment with IMT in combination with other therapies, to evaluate CAML PD-L1 prior to and post IMT induction (∼47 days) with clinical outcome analysis at 2 years. Methods In a prospective pilot study of previously treated MBC patients n=67, all starting new lines of systemic therapy in combination with IMT (pembrolizumab [n=57], nivolumab [n=2], or atezolizumab [n=8]) with active progressive metastatic disease. Of the patients, median age was 58.2 (range: 32-73). Median prior lines of therapy in the metastatic setting was 2 (range 0-14). Race demographics (Caucasian=43, Black=7, Hispanic=4, Asian=3 & unknown/other=11). ECOG 0 (n=34) and ECOG 1 (n=33). Visceral metastasis (n=43) and non-visceral (n=24). ER positivity was 37% (n=25), PR positivity was 39% (n=26), HER2 positivity was 13% (n=9) and 52% were triple negative breast cancer (n=35). Histology was IDC (n=52), Other (n=11), ILC (n=2), & IBC (n=2). We isolated CAMLs from 7.5 ml baseline (T0) blood using the LifeTracDx® PD-L1 test and scored PD-L1 as high or low. If possible, a follow-up sample (T1) was taken (∼47 days) after IMT induction. Patient’s progressive free survival (PFS) and overall survival (OS) hazard ratios (HRs) were analyzed by censored univariate analysis based on RECIST v1.1 over 2 years. Results Baseline T0 PD-L1 CAML data was available for 94% (n=63/67) of patients, with 44% (n=28/63) having high CAML PD-L1 which was not correlated with improved PFS (HR=1.3, 95%CI=0.7-2.3, p=0.5376) or OS (HR=1.3, 95%CI=0.7-2.5, p=0.5915). T1 PD-L1 CAML data was available for 78% (n=52/67) of patients, with 58% (n=30/52) having high CAML PD-L1 which significantly correlated with improved PFS (HR=3.1, 95%CI=1.3-7.2 p=0.0170,) and improved OS (HR=4.2, 95%CI=1.6-11.4, p=0.0102). In comparing CAML PD-L1 change post IMT, it was found that consistently low PD-L1 at T0 & T1 had the poorest responses, median PFS (mPFS)=2.2 months and median OS (mOS)=7.2 months. In contrast, patients who increased CAML PD-L1 after IMT induction had better responses, mPFS=6.3 months and mOS=13.1 months. Further, patients with consistently high PD-L1 at T0 & T1 had the best response rates, mPFS=9.5 months and mOS=19.7 months. Conclusion Here we describe a blood-based biopsy which can monitor dynamic PD-L1 changes in circulating tumor immune cells and may predict enhanced clinical benefit to PD-L1 IMTs in MBC. While an initial pilot study on a small population of patients, PD-L1 expression on CAMLs appears to identify patients with improved IMT responses and suggests larger validation studies are needed. Citation Format: D. L. Adams, M. Cristofanilli, C. Reduzzi, W. V. Williams, G. Del Priore, S. Chumsri, T. Iwase, N. T. Ueno, A. B. Duffy, C. Tang. Monitoring Upregulation of PD-L1 in Cancer Associated Macrophage-Like Cells in Blood Predicts Clinical Outcomes in Metastatic Cancer Patients Treated with PD-L1 Immunotherapies [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 PS2-09-25.

Clinical Cancer ResearchVol. 32(4_Supplement)
Cornell University (US), Cancer Center of Hawaii (US), Creatv MicroTech (United States) (US), United Therapeutics (United States) (US), Mayo Clinic in Florida (US)
Good health and well-being
Openalex Percentile: Top 47%
Immune cells in cancer
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.