Treatment-Refractory Triple-Negative Breast Cancer Treated With Tumor-Infiltrating Lymphocytes

This breast cancer diagnosis at a glance

Stage at diagnosis
Stage IV
Subtype
Invasive Lobular Carcinoma
Biomarkers
Germline BRCA1 pathogenic variant; later triple-negative phenotype
Sex
female
Spread to
skin, lungs, bones
Treatment
chemotherapy, surgery, radiation, targeted therapy and immunotherapy
Outcome
In Memory

Treatment course, step by step

  1. Received doxorubicin plus cyclophosphamide, followed by paclitaxel with carboplatin before surgery.
  2. Underwent bilateral mastectomy and then chest-wall and axillary radiation.
  3. After metastatic progression, received capecitabine, olaparib, pembrolizumab with palliative skin radiation, sacituzumab govitecan, and later additional systemic therapy.
  4. Received an experimental tumor-infiltrating lymphocyte infusion with lymphodepleting chemotherapy and IL-2.
  5. IL-2 was stopped after severe toxicity.

What happened, in summary

A 31-year-old woman was diagnosed with locally advanced cancer in her right breast in 2020. Imaging showed two breast tumors and marked axillary lymph-node involvement without distant disease. The initial biopsy showed mixed invasive ductal and lobular carcinoma, and germline testing identified a pathogenic BRCA1 variant.

She received doxorubicin plus cyclophosphamide, then paclitaxel with carboplatin, followed by bilateral mastectomy. The surgical specimen showed residual disease with 7 of 8 lymph nodes involved and a triple-negative phenotype. She completed radiation to the chest wall and axilla, but soon developed skin and lung metastases. Over the following course she received capecitabine, olaparib, pembrolizumab with palliative skin radiation, sacituzumab govitecan, and other systemic therapy as the cancer continued to progress into the lungs and bones.

With few options remaining, she underwent experimental tumor-infiltrating lymphocyte therapy after lymphodepleting chemotherapy. IL-2 had to be stopped after severe toxicity including shock, kidney failure, myocarditis, and heart failure. Her tumor burden briefly decreased and she was discharged, but the cancer rapidly relapsed. She died about 1 month after the TIL and IL-2 treatment began.

Where this story comes from

This is a lay summary of an account first published by PMC / PubMed Central. Read the original in full

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