# Detection of circulating tumor cells that predicts the efficacy of neoadjuvant chemotherapy for locally advanced triple-negative breast cancer

**Authors:** Cong Wang, Jingyue Li, Tingli Luo, Shenglin Zhu, Mingda Zhao, Yicai Jia, Yefu Liu

PMC · DOI: 10.3389/fmed.2025.1536971 · Frontiers in Medicine · 2025-04-30

## TL;DR

This study shows that tracking circulating tumor cells and stem cells can predict how well chemotherapy works for a type of breast cancer, earlier than current methods.

## Contribution

The study introduces a novel method using CTCs and CTSCs to predict chemotherapy resistance and efficacy in triple-negative breast cancer.

## Key findings

- Positive CTSCs after the first chemotherapy cycle predicted resistance with 91% specificity.
- A gradual decline in CTCs during the first cycle predicted treatment efficacy with 87% sensitivity and 80% specificity.
- CTCs and CTSCs can detect treatment outcomes up to six weeks earlier than the RECIST standard.

## Abstract

This study aims to assess the predictive potential of circulating tumor cells (CTCs) and circulating tumor stem cells (CTSCs) in locally advanced triple-negative breast cancer (TNBC) undergoing neoadjuvant chemotherapy (NAC) compared to the RECIST 1.1 standard.

We analyzed 112 patients with TNBC at the Liaoning Tumor Hospital. CTCs and CTSCs were evaluated before NAC, on the first NAC cycle day, and after NAC. We assessed the ability of positive CTSCs after the first cycle to predict NAC resistance (requiring regimen change) with a 91% specificity. Additionally, we analyzed CTC dynamics during the first NAC cycle to predict efficacy (often reaching MP4 or MP5) with 87% sensitivity and 80% specificity.

Positive CTSCs post-first cycle predicted NAC resistance with high specificity (91%). The gradual decline in CTCs during the first NAC cycle indicated NAC efficacy, allowing the regimen to continue with a sensitivity of 87% and specificity of 80%.

This study suggests that positive CTSCs after the first NAC cycle predict resistance, thereby facilitating early detection (≥ 6 weeks earlier than RECIST). Gradual CTC reduction during the first cycle predicts efficacy, enabling regimen continuation. CTCs and CTSCs show promise as predictive markers for NAC efficacy in patients with locally advanced TNBC.

## Linked entities

- **Diseases:** triple-negative breast cancer (MONDO:0005494), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, PROM1 (prominin 1) [NCBI Gene 8842] {aka AC133, CD133, CORD12, MCDR2, MSTP061, PROML1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, LAMTOR3 (late endosomal/lysosomal adaptor, MAPK and MTOR activator 3) [NCBI Gene 8649] {aka MAP2K1IP1, MAPBP, MAPKSP1, MP1, PRO0633, Ragulator3}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}
- **Diseases:** necrosis (MESH:D009336), breast cancer (MESH:D001943), colorectal cancer (MESH:D015179), metastasis (MESH:D009362), invasive ductal carcinoma (MESH:D044584), TNBC (MESH:D064726), Tumor (MESH:D009369), CTSCs (MESH:D009360)
- **Chemicals:** formamide (MESH:C031066), ethanol (MESH:D000431), CS2 (MESH:D002246), DAPI (MESH:C007293), sodium citrate (MESH:D000077559), Alexa Fluor 594 (-), fluorescein (MESH:D019793)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12075245/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12075245/full.md

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Source: https://tomesphere.com/paper/PMC12075245