
Combination Treatment Benefits Patients With Advanced Breast Cancer That Has Spread to Brain
Key Takeaways
- A 17-patient cohort with HER2+ breast cancer leptomeningeal metastasis achieved median OS of 10 months, exceeding historical 4.4 months, with 41% survival at 18 months.
- Central nervous system disease control was observed with a median seven months to CNS progression, and neurologic deficits improved in 7 of 12 evaluable patients.
Tucatinib and trastuzumab, plus capecitabine, may improve symptoms and extend survival in some breast cancer patients with leptomeningeal metastasis.
Patients with leptomeningeal metastasis (LM) have historically had few treatment options. Now, researchers from The University of Texas MD Anderson Cancer Center have found a combination of targeted therapies, tucatinib and trastuzumab, plus the chemotherapy drug, capecitabine, may improve symptoms and extend survival in some
The Phase II study, published today in
“The combination achieved a clinically meaningful improvement in overall survival compared to historical controls,” said lead author
Why are there limited treatments for patients with leptomeningeal metastasis?
Leptomeningeal metastasis is difficult to treat primarily because the blood-brain barrier may block drugs from reaching the spinal fluid, where the metastatic cells are found. Additionally, LM is not a solid tumor but is made up of metastatic cells living in fluid, making them more difficult to target. Historically, there also are few studies about this specific disease.
“In addition to encouraging survival outcomes, throughout this study we observed improvements in neurologic symptoms,” said co-lead author
How do the treatments in this combination therapy work?
Tucatinib is a
The single arm, non-randomized, multi-phase study enrolled patients at four sites in the U.S., including UT MD Anderson. Eligible patients were at least 18 years old with histologically proven metastatic HER2+ breast carcinoma. These patients were treated with 21-day cycles of oral tucatinib (300 mg) twice daily, plus oral capecitabine (1000 mg/m2) twice daily on days 1-14 and intravenous trastuzumab (6 mg/kg) on day 21.
What are other key findings of the study?
Side effects included diarrhea, nausea, vomiting, hand-foot syndrome, and liver function test elevation. Most adverse effects improved or resolved with appropriate care and dose modifications. One patient saw alanine aminotransferase elevation after one cycle, which led to discontinuation of the combination, and symptoms resolved after one month.
Study limitations include early termination due to slow accrual following Food & Drug Administration (FDA) approval of the combination therapy. Additionally, LM from HER2+ metastatic breast cancer is rare, resulting in limited published data. As a result, the study design was informed by the small amount of available retrospective evidence.
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This study was sponsored by Translational Breast Cancer Research Consortium and its foundation partners: the Breast Cancer Research Foundation and Susan G. Komen and Seagen Inc. For a full list of collaborating authors, disclosures and funding sources, see the full paper in


















































































