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Oseltamivir as rescue therapy for persistent, chronic, or refractory immune thrombocytopenia: a case series and review of the literature

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Abstract

Immune thrombocytopenia (ITP) is an autoimmune disease that results from antibody-mediated platelet destruction and impaired platelet production. Novel therapies have emerged in the last decade, but 15–20% of patients will relapse or fail and require further therapy. We performed a prospective, single-arm intervention study on seven patients with chronic, persistent, or refractory ITP from the Hospital Universitario “Dr. José E González”, in Monterrey, Mexico between 2015 and 2019. Eligible patients received oral oseltamivir 75 mg twice daily for 5 days and were followed up for six months. Most patients received a median of three distinct therapies (range 2–6). Four patients (57.1%) received combined therapy. The median time for any response was 55.5 days (range = 14–150). All patients responded at some point in time (ORR = 100%, six had a proportion of loss of response [PR], and one achieved [CR]). Six months after oseltamivir administration, three patients (42.9%) maintained a response, and one patient had a CR (14.3%). Oseltamivir was well tolerated with a good overall response rate and was useful for treating chronic ITP. We observed an initial increase in the number of platelets; however, this response was not maintained.

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Funding

The research was financed by the Hematology Service of the Universidad Autonoma de Nuevo Leon, Monterrey, México.

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Correspondence to David Gómez-Almaguer.

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Informed consent was obtained from all individual participants included in the study.

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Colunga-Pedraza, P.R., Peña-Lozano, S.P., Sánchez-Rendón, E. et al. Oseltamivir as rescue therapy for persistent, chronic, or refractory immune thrombocytopenia: a case series and review of the literature. J Thromb Thrombolysis 54, 360–366 (2022). https://doi.org/10.1007/s11239-022-02651-3

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  • DOI: https://doi.org/10.1007/s11239-022-02651-3

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