An expert discusses the expanded treatment options for refractory ITP, emphasizing accurate diagnosis, combination therapies targeting platelet production and destruction, and the evolving role of splenectomy with improved safety measures.
For patients with very refractory ITP, treatment options have expanded significantly over the years. However, the first step is to confirm the diagnosis — ensuring that it truly is ITP and not another condition causing the low platelet count. This might involve ruling out other factors like drug interactions or considering a bone marrow biopsy, especially in older individuals whose platelet counts are not improving.
In cases of refractory ITP, combining therapies with different mechanisms can be effective. For example, using a TPO receptor agonist to boost platelet production alongside fostamatinib, which targets platelet destruction, may work synergistically to improve platelet counts. Exploring such combinations can provide additional benefit for patients who don’t respond well to single agents.
Historically, splenectomy has been a treatment option for refractory ITP, offering the potential for sustained long-term response. Before surgery, patients are vaccinated against encapsulated bacteria and may require antibiotics depending on their immune status. The procedure can be done laparoscopically or, rarely, via open surgery. Advances in surgical techniques have improved the success rates and safety of splenectomy in recent years.
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