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Treatment of HER2-Positive Brain Metastasis from Cervical Cancer Using Multimodal Therapy Including Pyrotinib: A Case
Yuanping Chen1, Ting Wen2, Xinglin Wen3
1Department of Oncology, Ganzhou Hospital-Nanfang Hospital, Southern Medical University (Ganzhou People's Hospital), Ganzhou, People's Republic of China.
Abstract:
Cervical cancer with brain metastasis is uncommon and generally associated with poor prognosis. Overexpression of human epidermal growth factor receptor 2 (HER2) represents a promising therapeutic target in gynecological malignancies. We report a patient with International Federation of Gynaecology and Obstetrics (FIGO) stage IVb cervical adenosquamous carcinoma who developed a solitary brain metastasis following chemoradiotherapy. She underwent surgical resection, and immunohistochemistry of the postoperative specimen demonstrated HER2 overexpression (3+). Postoperatively, she received radiotherapy and systemic therapy with pyrotinib and capecitabine, achieving a complete response with manageable toxicity. Her progression-free survival was nearly 29 months (from brain metastasis resection to last follow-up). This case illustrates successful management of HER2-positive brain metastases from cervical cancer using a multimodal approach combining surgery, radiotherapy, and systemic therapy with pyrotinib and capecitabine. The durable complete response with manageable toxicity underscores the therapeutic potential of HER2-targeted therapy as part of a multimodal regimen; however, further studies are required to validate these findings and optimize personalized treatment strategies.
Insights
A rare case of HER2-positive cervical cancer brain metastasis was successfully treated with surgery, radiation, and targeted therapy (pyrotinib and capecitabine), achieving a near 29-month progression-free survival.
Area of Science:
- Oncology
- Neurology
- Genetics
Background:
- Cervical cancer brain metastasis is rare and has a poor prognosis.
- Human epidermal growth factor receptor 2 (HER2) overexpression is a targetable marker in gynecological cancers.
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