Clinical Effects of Hypomethylating Agents in Patients with Newly Diagnosed Myelodysplastic Syndrome Who Received DNA-Damaging Chemotherapy for Metastatic Breast Cancer.
Dong Won BaekSoo Jung LeeSang Kyun SohnJoon-Ho MoonYee Soo ChaePublished in: Journal of breast cancer (2019)
The cumulative risk of therapy-related myelodysplastic syndrome (t-MDS) in breast cancer patients exposed to chemotherapy and/or radiotherapy is significantly high compared to that in other cancer patients. This report reviews the use of hypomethylating agents (HMAs) to treat a 57-year-old woman newly diagnosed with MDS during palliative chemotherapy for metastatic breast cancer. Over a period of 6 years, the patient received several DNA-damaging chemotherapeutics including doxorubicin, cyclophosphamide, and paclitaxel. Repeated thrombocytopenia was the main reason for suspecting secondary hematologic malignancy. She was diagnosed with t-MDS based on bone marrow examination and her treatment history for breast cancer. While azacitidine was originally administered to stabilize MDS, it also stabilized the patient's lung and lymph node metastases without any major toxicity. Therefore, the current case highlights the promising effects of HMAs for treating t-MDS following heavily pretreated breast cancer.
Keyphrases
- metastatic breast cancer
- newly diagnosed
- locally advanced
- lymph node
- bone marrow
- circulating tumor
- case report
- neoadjuvant chemotherapy
- cell free
- early stage
- rectal cancer
- single molecule
- acute myeloid leukemia
- radiation therapy
- chemotherapy induced
- mesenchymal stem cells
- oxidative stress
- drug delivery
- squamous cell carcinoma
- low dose
- stem cells
- high dose
- randomized controlled trial
- palliative care
- cancer therapy
- nucleic acid
- smoking cessation
- circulating tumor cells