ArticleCureus2025
Triple-Negative Metaplastic Breast Cancer Ameliorated Following KEYNOTE-522: A Case Report.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Long-Term Response to Pembrolizumab in Metastatic Metaplastic Breast Carcinoma: A Case Report.The American journal of case reports · 2026Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Metaplastic breast cancer (MpBC) is a rare and aggressive subtype of breast cancer, with the triple-negative variant (TN-MpBC) being particularly resistant to standard systemic therapies and associated with poor outcomes. We present the case of a 48-year-old African American female diagnosed with TN-MpBC, incidentally identified during cardiac evaluation for sarcoidosis. Imaging and biopsy revealed a 5.8 cm high-grade tumor with a Ki-67 index above 30%. The patient was treated with the KEYNOTE-522 regimen, which includes neoadjuvant chemotherapy (NAC) (paclitaxel, carboplatin, doxorubicin, and cyclophosphamide) and pembrolizumab immunotherapy. Post-treatment imaging demonstrated substantial tumor regression, and subsequent bilateral mastectomy confirmed a complete pathological response with no residual malignancy. She is currently undergoing adjuvant pembrolizumab and proton radiation therapy. Given the historically poor response of TN-MpBC to chemotherapy alone, this case illustrates the promising role of immunotherapy, particularly in programmed death-ligand 1 (PD-L1)-expressing tumors. It supports emerging evidence that chemoimmunotherapy combinations such as KEYNOTE-522 may improve prognosis in TN-MpBC, emphasizing the need for continued investigation into targeted therapeutic strategies for this challenging breast cancer subtype.
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Registered trials
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