Paroxysmal nocturnal hemoglobinuria testing in patients with myelodysplastic syndrome in clinical practice-frequency and indications
| Autor: | Heather A. Leitch, Dalal Bi, Wong Sa |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Adult
Male medicine.medical_specialty Anemia Hemoglobinuria Paroxysmal CD59 Gastroenterology hemic and lymphatic diseases Internal medicine Biopsy medicine Humans Clinical significance Aged CD64 Aged 80 and over biology medicine.diagnostic_test business.industry Haptoglobin Middle Aged medicine.disease Myelodysplastic Syndromes Paroxysmal nocturnal hemoglobinuria biology.protein Hemoglobinuria Female Original Article business |
| Zdroj: | Current oncology (Toronto, Ont.). 25(5) |
| ISSN: | 1718-7729 |
| Popis: | Background Myelodysplastic syndrome (mds) is characterized by peripheral blood cytopenias, with most patients developing significant anemia and dependence on red blood cell (rbc) transfusion. In paroxysmal nocturnal hemoglobinuria (pnh), mutations in the PIGA gene lead to lack of cell-surface glycosylphosphatidylinositol, allowing complement-mediated lysis to occur. Paroxysmal nocturnal hemoglobinuria results in direct antiglobulin test–negative hemolysis and cytopenias, and up to 50% of patients with mds test positive for pnh cells. We wanted to determine whether pnh is considered to be a contributor to anemia in mds. Methods Patients with a diagnosis of mds confirmed by bone-marrow biopsy since 2009 were reviewed. Highresolution pnh testing by flow cytometry examined flaer (fluorescein-labeled proaerolysin) binding and expression of CD14, CD15, CD24, CD45, CD59, CD64, and CD235 on neutrophils, monocytes, and rbcs. Results In 152 patients with mds diagnosed in 2009 or later, the mds diagnosis included subtypes associated with pnh positivity (refractory anemia, n = 7, and hypoplastic mds, n = 4). Of 11 patients who underwent pnh testing, 1 was positive (9.0%). Reasons for pnh testing were anemia ( n = 3), new mds diagnosis ( n = 2), hypoplastic mds ( n = 2), decreased haptoglobin ( n = 1), increased rbc transfusion requirement ( n = 1), and unexplained iron deficiency ( n = 1). Conclusions Testing for pnh was infrequent in mds patients, and the criteria for testing were heterogeneous. Clinical indicators prompted pnh testing in 6 of 11 patients. Given that effective treatment is now available for pnh and that patients with pnh-positive mds can respond to immunosuppressive therapy, pnh testing in mds should be considered. Prospective analyses to clarify the clinical significance of pnh positivity in mds are warranted.in clinical practice, with manageable toxicity. |
| Databáze: | OpenAIRE |
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