# Neoadjuvant TACE combined with chemo-immunotherapy for giant triple-negative breast cancer: a case report

**Authors:** Jie Tan, Zhuo Li, Zhi-Jun Li, Feng-Lin Kang, Hua Xiang, Peng Yan

PMC · DOI: 10.3389/fimmu.2026.1739817 · Frontiers in Immunology · 2026-02-18

## TL;DR

A woman with a large, advanced breast cancer received a combination of local and systemic treatments, leading to significant tumor shrinkage and successful surgery.

## Contribution

This case report introduces a novel multimodal treatment approach combining TACE with chemo-immunotherapy for extreme TNBC cases.

## Key findings

- The multimodal treatment led to marked tumor regression and healing of skin ulceration.
- Postoperative pathology showed a complete response with no residual tumor.
- The approach may enhance local control and synergistic immune activation in extreme TNBC cases.

## Abstract

Giant, ulcerated triple-negative breast cancer (TNBC) presents major therapeutic challenges. We report a 39-year-old woman with a 14.3 cm ulcerated TNBC (cT4bNxM0) who developed infection after intravenous chemotherapy. To achieve rapid local control, a multidisciplinary team elected to perform transarterial chemoembolization (TACE), followed by systemic chemo-immunotherapy using nab-paclitaxel and the PD-1 inhibitor Toripalimab. This multimodal approach led to marked tumor regression and improvement of skin ulceration, enabling curative surgery with modified radical mastectomy and complex reconstruction. Pathology postoperative showed a complete response (Miller-Payne grade 5, ypT0N0M0). This single case suggests that integrating TACE with multimodal neoadjuvant treatment sequences may be feasible in selected patients with extreme presentations of locally advanced TNBC, particularly in patients with extensive tumor burden or poor tolerance to systemic therapy. The approach may enhance local control and elicit synergistic immune activation, offering a potential paradigm for managing extreme TNBC presentations. Further studies are required to clarify the safety, efficacy, and potential immunomodulatory effects of this approach.

## Linked entities

- **Chemicals:** nab-paclitaxel (PubChem CID 36314)
- **Diseases:** triple-negative breast cancer (MONDO:0005494), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** HMGB1 (high mobility group box 1) [NCBI Gene 3146] {aka HMG-1, HMG1, HMG3, SBP-1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CALR (calreticulin) [NCBI Gene 811] {aka CALR1, CRT, HEL-S-99n, RO, SSA, cC1qR}, ADAM17 (ADAM metallopeptidase domain 17) [NCBI Gene 6868] {aka ADAM18, CD156B, CSVP, HYPT16, NISBD, NISBD1}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, SOX10 (SRY-box transcription factor 10) [NCBI Gene 6663] {aka DOM, PCWH, SOX-10, WS2E, WS4, WS4C}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** osseous (MESH:C535395), Granulomas (MESH:D006099), liver dysfunction (MESH:D017093), embolization (MESH:D004617), invasive ductal carcinoma (MESH:D044584), TNBC (MESH:D064726), Giant breast cancer (MESH:D001943), reactive (MESH:D000275), sepsis (MESH:D018805), hepatocellular carcinoma (MESH:D006528), ischemia (MESH:D007511), necrosis (MESH:D009336), hyperplasia (MESH:D006965), fever (MESH:D005334), pain (MESH:D010146), skin (MESH:D012871), Inflammatory (MESH:D007249), H&amp;E (MESH:D016751), liver metastases (MESH:D009362), toxicity (MESH:D064420), ulcer (MESH:D014456), liver and lung cancers (MESH:D008175), infection (MESH:D007239), skin ulcers (MESH:D012883), cancer (MESH:D009369), reactive hyperplasia (MESH:D019310)
- **Chemicals:** lipid (MESH:D008055), ATP (MESH:D000255), cholesterol (MESH:D002784), cyclophosphamide (MESH:D003520), taxane (MESH:C080625), anthracycline (MESH:D018943), Carboplatin (MESH:D016190), epirubicin (MESH:D015251), platinum (MESH:D010984), KEYNOTE-522 (-), H&amp;E (MESH:D006371), Toripalimab (MESH:C000656314), pembrolizumab (MESH:C582435), paclitaxel (MESH:D017239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12956800/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956800/full.md

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Source: https://tomesphere.com/paper/PMC12956800