To cite this paper use one of the standards below:
Case report:
We report three female patients diagnosed with relapsing-remitting multiple sclerosis (RRMS) undergoing therapy with high-efficacy drugs, including Natalizumab, Ocrelizumab, and Fingolimod. During treatment, they were diagnosed with breast nodules (BN) and initially chose clinical monitoring. The first patient, aged 36, monitored a BN with a specialist since 2018, starting Ocrelizumab treatment. After three months, she was diagnosed with breast cancer. The second patient, aged 45, followed a BN with a specialist since 2015, starting Fingolimod in 2018 and undergoing a breast biopsy that year, revealing ductal hyperplasia. After partial breast resection in 2019, she relapsed, switching to Natalizumab and experiencing cancer recurrence. The third patient, aged 38, rejected conventional treatment, opting for high-dose vitamin D therapy despite medical recommendations for disease modifying drugs (DMD). Due to new relapses and increased lesion burden, she started Natalizumab, later diagnosed with ductal carcinoma in situ, leading to bilateral mastectomy.
Discussion:
Multiple sclerosis (MS) is an autoimmune inflammatory disease of the central nervous system affecting young women globally, altered by disease modifying therapy (DMT). Despite proven efficacy, recent studies suggested potential adverse effects, including neoplasms like breast cancer. Many patients already have BN before DMT, lacking regular screening. Breast cancer is prevalent among women worldwide, and its diagnosis may result from disease progression or missed screening. Three patients with prior breast nodule follow-up, diagnosed with RRMS on high-efficacy therapy, are presented, two with malignant breast neoplasia.
Final Comments:
Although breast neoplasia occurred in the three patients, causality with disease-modifying drugs cannot be established. Further research is needed to understand their potential adverse effects. Implementing neoplasm screening protocols for patients on DMT is crucial.
With nearly 200,000 papers published, Galoá empowers scholars to share and discover cutting-edge research through our streamlined and accessible academic publishing platform.
Learn more about our products:
This proceedings is identified by a DOI , for use in citations or bibliographic references. Attention: this is not a DOI for the paper and as such cannot be used in Lattes to identify a particular work.
Check the link "How to cite" in the paper's page, to see how to properly cite the paper