- Giovanni Emilia⇓,
- Mario Luppi,
- Monica Morselli,
- Fabio Forghieri,
- Leonardo Potenza and
- Giuseppe Torelli
- Department of Oncology and Hematology, Division of Hematology, University of Modena and Reggio Emilia, Italy
- Correspondence: Giovanni Emilia, M.D., Department of Oncology and Hematology, Policlinico, via del Pozzo 71, 41100 Modena, Italy. Phone: international +39.059.4222197. Fax: international +39.059.4224549. E-mail:
Management of patients with severe, refractory, chronic immune thrombocytopenic purpura (ITP) is still difficult. However, although there is no consensus on the best treatment strategy, these patients show a persistent, marked thrombocytopenia, and need therapy, owing to the presence of or to an increased risk of bleeding. Various treatments have been attempted: immunosuppressive chemotherapy, high-dose dexamethasone, danazol, combination chemotherapy, which have shown transient response in a variable percentage of cases, but none with any evidence of safe and durable efficacy.1 Recently, a systematic review of more than 300 patients treated with a monoclonal anti-CD20 antibody, rituximab, many of whom with a severe form of ITP, has shown an overall platelet response of 62.5%, a median response duration of 10.5 months, but also significant toxicities. Therefore, the optimal timing and dose of the drug remain undefined.2 More recently, good results have been reported with a multiagent induction and maintenance therapy, even if the duration of response was not defined.3 Furthermore, an increase in platelet counts has been obtained using a thrombopoietin-receptor agonist, eltrombopag, though the durability of the response and the long-term safety of this compound are unknown.4 Finally, a promising further approach seems to be the active and safe use of low dose rituximab.5 As reported in published data, there are considerable side-effects associated with the current treatment and the responses of various therapies have not yet been consolidated. Other therapeutic strategies should, therefore, also be considered. There are few data in the literature describing the effects of cyclosporine (CyA) therapy in this setting. A study has been reported in adults in whom high toxicity offsets benefits,6 and this finding has also been confirmed in children.7 However, in both studies high doses of CyA (5–10 mg/kg/d) have been used.
We have already reported on long-term salvage therapy with CyA in 12 severe, refractory, chronic ITP8 with 83.3% of response (10/12), lasting for a median follow-up of 36.8 months. The patients were 9 women and 3 men (median age 66.6 years, range 42–85 years). All patients had previously received 2–3 drug therapies and 8 patients had also undergone splenectomy. Only patients with platelet counts less than 30×109/L entered the study. All patients had major or minor bleeding episodes, often transient, but recurrent. Results of a long-term follow-up of the responsive patients are shown in Table 1. The updated median follow-up of approximately 5.5 years (69 months, range 4–13 years), shows that 9 patients had maintained response for the duration of the observation period (Figure 1). A further patient, not considered for the follow-up (n.8) died in complete remission of myocardial infarction during a 3-month course of CyA treatment. Five patients (ns. 1,2,7,9,and 10) had a complete response (platelet counts in normal range), one patient (n. 5) had a partial response (platelet counts between 80 and 150×109/L), and 2 patients (ns. 3 and 12) had a complete response which had been maintained with continued drug administration. One patient (n. 4) had a drug-dependent complete response for approximately 4.5 years and a partial response for a further 1.5 year, after CyA had been tentatively discontinued and then restored. Two patients (ns. 10 and 4) had a relapse at 5 and 6.5 years, respectively, and 1 patient (n. 3) died at seven years. The drug dose was 2.5–3 mg/kg/d, after a starting dose of 5 mg/kg/d for six days, to maintain a therapeutic serum level between 200 and 400 ng/mL. Patient monitoring included monthly blood cell counts and examination of CyA serum level, renal and hepatic functions every week for one month, then every two months and every six months, after a stable remission had been achieved. Platelet counts usually began to increase after 3–4 weeks of treatment. A further reduction of daily dose of CyA could be obtained by the co-administration of grapefruit juice. The side-effects were minor, transient and reversible, even after long-term, continued treatment. Intolerance manifestations usually resolved spontaneously or with a dose reduction of CyA or its withdrawal for a few days. Only an infectious episode (candidiasis, pt. n. 7) was recorded, which was rapidly resolved by standard antifungal therapy and discontinuation of CyA for few days. Only one patient (n. 3) showed a creatinine increase exceeding 150% of the baseline value, resolved by a CyA dose reduction of 25% for ten days. Similar results were recently obtained in adults, in a smaller series with shorter follow-up, by others9 and also in children.10 Furthermore, CyA has recently been recommended as a second-line therapy in Evans’ syndrome.11
The persistently high rate of responses, and the low and transient toxicities, recorded after such a long-term follow-up, suggest that the oral administration of low-dose CyA, could be considered in severe, refractory ITP as a salvage therapy and/or as a maintenance treatment after a response has been obtained by rituximab or more aggressive approaches.
We have been using this approach in our current clinical practice and believe that the debated issue of CyA-related toxicity largely relies on the use of higher doses of the drug and can be otherwise easily managed by the use of standard or even lower doses of the drug and by a routine assessment of patients’ clinical and laboratory parameters. Therefore, we encourage further studies on larger series of patients to assess the general relevance of our findings. We also suggest that patients with refractory ITP, screened positive for Helicobacter pylori (Hp) infection should undergo bacterium eradication before or after CyA as reported,12 at least in areas with a high prevalence of Hp infection.
- Copyright© Ferrata Storti Foundation