Case Report: Effective Treatment With Pyrotinib and Capecitabine in a Heavily Pretreated Locally Advanced Breast Cancer Harboring Both HER2 Overexpression and Mutant
HER2 positive
03 medical and health sciences
breast cancer
0302 clinical medicine
Oncology
pyrotinib
L775S
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
ERBB2 mutant
RC254-282
3. Good health
DOI:
10.3389/fonc.2021.715554
Publication Date:
2021-10-14T07:44:47Z
AUTHORS (5)
ABSTRACT
The prognosis for female patients with locally advanced breast cancer (LABC) has improved the emergence of novel drugs, especially those who have HER2 overexpression or ERBB-2 amplification. Trastuzumab-based regimen been paradigm in guidelines as first-line therapy, whereas many got progressive disease after several cycles treatment rapidly progress because primary resistance. Point mutations ERBB2 gene occur both HER2-amplication and non-amplification patients, a 2% ratio cohort 1.48% amplication population. acquired mutation substantially raised to 16.7%–17.7% prior trastuzumab treatment. may be critical reason resistance progression among treated anti-HER2 monoclonal dual antibodies pertuzumab, tyrosine-kinase inhibitor. L755S V842I indicates trastuzumab, while that K753I lapatinib; these maybe sensitive pan-HER inhibitors. A 48-year woman diagnosed HER2-positive LABC developed three lines cross-line partial response (PR) best response. tissue was performed by next-generation sequencing (NGS), results discovered gene. Then, she received effective pyrotinib plus capecitabine underwent mastectomy six combined PR. Subsequently, performed, took 1 year monotherapy another adjuvant therapy achieved long-term clinical benefit. In conclusion, is potential neoadjuvant agent are heavily pretreated harbor amplification mutant cancer.
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