scholarly journals One year follow-up of children and adolescents with chronic immune thrombocytopenic purpura (ITP) treated with rituximab

2009 ◽  
Vol 52 (2) ◽  
pp. 259-262 ◽  
Author(s):  
Brigitta U. Mueller ◽  
Carolyn M. Bennett ◽  
Henry A. Feldman ◽  
James B. Bussel ◽  
Thomas C. Abshire ◽  
...  
Blood ◽  
2008 ◽  
Vol 112 (4) ◽  
pp. 999-1004 ◽  
Author(s):  
Bertrand Godeau ◽  
Raphael Porcher ◽  
Olivier Fain ◽  
François Lefrère ◽  
Pierre Fenaux ◽  
...  

Abstract Whether rituximab could effectively and safely avoid splenectomy for adults with chronic immune thrombocytopenic purpura (ITP) remains unresolved. A multicenter, prospective, open-label, single-arm, phase 2 trial was conducted to assess rituximab safety and efficacy in adult splenectomy candidates with chronic ITP. Sixty patients with chronic (≥ 6 months) ITP and platelet counts less than 30 × 109/L received a weekly intravenous infusion of rituximab (375 mg/m2) for 4 weeks. All other ITP treatments were stopped. A good response was defined as a platelet count 50 × 109/L or more, with at least a doubling of the initial value at 1 and 2 years after the first rituximab infusion. Patients who required another treatment during follow up were considered nonresponders. Sixteen patients experienced transient side effects that necessitated treatment discontinuation for only 1. Good 1-year responses were obtained in 40% of the patients (24/60 [95% confidence interval: 28%-52%]). At 2 years, 33.3% (20/60 patients) had good responses and 6.7% (4/60) had sustained platelet counts of 30 × 109/L or more without treatment. Thirty-six (60%) patients failed to respond; 25 underwent splenectomy. Based on these results, rituximab was an apparently safe and effective splenectomy-avoiding option in some adults with chronic ITP. This trial is registered at http://clinicaltrials.gov as NCT00225875.


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4462-4462
Author(s):  
Mehdi Khellaf ◽  
Laurent Eckert ◽  
Priscille Poitrinal ◽  
Camille Francesconi ◽  
Albert Haddad ◽  
...  

Abstract Abstract 4462 Background and objectives The treatment of chronic immune thrombocytopenic purpura (ITP) requires therapies which vary considerably in type, duration, and cost. The impact of ITP on resource utilization and direct healthcare costs in France is currently unknown. Yet it is crucial to gain a better understanding of the cost of ITP, particularly in its chronic form, in order to determine the value of new therapies in this therapeutic area. We report here the annual costs in a group of patients with chronic ITP enrolled consecutively and followed for a period of one year in a single French reference center. Design and Methods This is a single-center, single-arm, retrospective, observational cohort study in which adult (>18 years) patients with chronic ITP (diagnosed as per ASH guidelines) were enrolled and followed for at least one year. Patients with secondary ITP were excluded. Resource utilization and costs for treatments (drugs and splenectomy) and hospitalization/visits were estimated over a one-year follow-up, from a French public hospital perspective. Costs per patient were estimated (mean), and bootstrapping methods were used to calculate 95% confidence intervals (as cost data are not normally distributed). Healthcare resource utilization was analyzed for the entire population (whole group) and in two subgroups in which patients had a more severe form of the disease. The first subgroup (subgroup 1) included patients who were admitted to the hospital during the one-year study period for ITP treatment, treatment of side effects related to ITP treatment, or bleeding symptoms. Among them, we selected a second subgroup (subgroup 2) in which the severity of the disease required at least one intravenous immunoglobulin (IVIg) infusion during the one-year study period. IVIg treatment is costly and commonly used as a rescue therapy in patients with ITP. Results A total of 57 consecutive patients (42F/15M) with a mean age of 48 years (SD: 19) at ITP diagnosis were studied. Mean platelet count at diagnosis was 28 ± 26×109/L. Mean length of ITP duration at the time of inclusion in the study was 3.1 years (SD: 2) and 8 patients had undergone splenectomy. Subgroup 1 included 27 patients (47%) who were admitted to the hospital during the one-year study period (full hospitalization, n=23; and/or day hospitalization, n=8). Among them, 12 patients (21%) received at least one IVIg infusion during the one-year study period and were included in subgroup 2. When severity was not considered (whole group), the total mean cost per patient for the one-year study period was €7,293 [3,369; 13,584]. In subgroup 1, of 27 patients with at least one hospitalization, costs rose substantially, with costs being roughly twice that of the whole group: €15,334 [7,876; 27,459] mean cost per patient. Finally, the most dramatic cost increase was observed in 12 patients who received IVIg (subgroup 2). Costs in this group were more than three times those in the whole group: €26,581 [12,241; 50,578] mean cost per patient. IVIg costs accounted for 50% of the whole group costs and up to 64% of costs when considering patients with the most severe disease. Interpretation and conclusion Management of adults with chronic severe ITP is costly in France, with IVIg use being a major cost driver. From a budget payer's perspective, the availability of therapeutic agents that could reduce the need for IVIg and emergency hospitalizations could mitigate the costs of current ITP treatments. As the present study investigated only a limited group of patients from a single center, further research to better understand the likely effect of new therapies on resource utilization and costs is warranted. Disclosures: Eckert: AMGEN: Employment. Poitrinal:AMGEN: Employment. Francesconi:AMGEN: Employment. Haddad:AMGEN: Employment. Riou França:AMGEN: Employment. Launois:AMGEN: Employment. Godeau:AMGEN: Consultancy.


2012 ◽  
Vol 101 (7) ◽  
pp. 761-766 ◽  
Author(s):  
Steen Rosthøj ◽  
Jukka Rajantie ◽  
Iris Treutiger ◽  
Bernward Zeller ◽  
Ulf Tedgård ◽  
...  

Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3983-3983
Author(s):  
Ibrahim N. Nakhoul ◽  
Ilan Shapira ◽  
May Abdo-Matkiwsky ◽  
Peter Kozuch ◽  
Etta Frankel ◽  
...  

Abstract Background: The goal of therapy of immune thrombocytopenic purpura (ITP) is to produce and maintain a platelet (PLT) count greater than 30,000/μL. While anti-Rh(D) produces a rapid PLT rise (43,000/μL median overnight increase), the median duration of response is short (46 days). More than 50% of patients treated intermittently with anti-Rh(D) continue to require therapy after one year. In contrast to anti-Rh(D), the time to response and duration of response with danazol are long (median 3.1 months, 119 months, respectively). Both agents are alternatives to splenectomy. We hypothesize that danazol is an anti-Rh(D)-sparing agent and that the addition of danazol to anti-Rh(D) may decrease the requirement for anti-Rh(D) and obviate the need for continued anti-Rh(D) after one year. Methods: This is a single arm, non-randomized, phase II trial, utilizing a single stage design to compare rates of discontinuance of anti-Rh(D) at the end of one and two years. A total of 26 patients will be recruited. Treatment consists of daily danazol 600 mg in combination with anti-Rh(D) 75 μg/kg IV on day 1, to be repeated whenever PLT falls below 30,000/μL. After 1 year, danazol will be reduced to 400 mg daily for 3 months then to 200 mg daily for 9 months. Results: Seven patients have been enrolled to date (5 men/2 women). The median patient age is 43 years (range 22–51 years). The clinical course on study is summarized in Table 1. Five patients are evaluable for efficacy. Four patients have required a median of 1.5 anti-Rh(D) infusions during a median study enrollment of 43.5 weeks. Three patients have had sustained responses following the initial infusion of anti-Rh(D) noted at 14 - 35 weeks of follow-up; a second course of anti-Rh(D) was required in one of these patients at 40 weeks of follow-up. One patient has developed progressive disease. Two patients were removed from protocol therapy due to danazol toxicities; they have maintained PLT greater than 30,000/μL 6 - 35 weeks after discontinuation. No patients were noncompliant with therapy. No treatment-related deaths occurred. Conclusion: The combination of anti-Rh(D) and danazol is a novel regimen for patients with ITP. While anti-Rh(D) provides an immediate effect, danazol provides maintenance therapy. The duration of response after the initial anti-Rh(D) infusion in three patients in this study appears longer than that in patients treated with anti-Rh(D) alone, but further accrual and follow-up will be required to define toxicity and efficacy. Efficacy of anti-Rh(D) and danazol as of 07/27/06 Pt. Pt. Prior therapy Duration of danazol therapy (wks) # of anti-Rh(D) infusions administered Toxicities Comments 1 Prednisone, Anti-Rh(D)x1 47 2 Second course of anti-Rh(D) was required 40 weeks after the initial course. 2 Dexamethasone, IVIG, Anti-Rh(D)x3 14 1 Gr 1 alopecia, Gr 2 myalgias Disenrolled due to toxicity. Has maintained PLT > 30,000/ μL 6 weeks after disenrollment. 3 None 43 1 4 Dexamethasone 44 9 5 Dexamethasone, IVIG 6 4 Gr 2 anemia Disenrolled due to progressive disease (retroperitoneal bleed). 6 Prednisone 6 1 Disenrolled due to technical limitations (lack of IV access). 7 Dexamethasone 3 1 Gr 3 acne Disenrolled due to toxicity. Has maintained PLT > 30,000/ μL 35 weeks after disenrollment.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 478-478 ◽  
Author(s):  
Bertrand Godeau ◽  
Olivier Fain ◽  
Raphael Porcher ◽  
Francois Lefrere ◽  
Pierre Fenaux ◽  
...  

Abstract Background : Rituximab, a monoclonal anti-CD20 antibody, is a promising therapeutic agent for adults with immune thrombocytopenic purpura (ITP). Pooling results of the published literature suggest that rituximab achieves an initial response in about 50 % of adults with chronic ITP, with a 25–40% rate of sustained response. However, heterogeneity of patient pre-treatment status, short follow up and bias due to retrospective studies limit the interpretation of the data. Objective : To assess the safety and efficacy of rituximab in adults with chronic ITP (duration ≥ 6 months) and platelet count ≤ 30x109/L candidate to splenectomy. Methods : a multicenter prospective open-label single arm phase 2 trial designed according to Fleming’s single stage procedure was conducted. After informed consent, non splenectomized adults received 4 weekly intravenous infusions of rituximab at a dose of 375 mg/m2. All other ITP treatments were stopped. Treatment success was defined as a platelet count ≥ 50 x109/L with at least a 2 fold increase of the initial value at one year after the first rituximab infusion. Patients who received another treatment during follow up were considered as non responders. A sample size of at least 56 patients was calculated by Fleming’s single-stage design to ensure 90 % power for proving lack of efficacy if the true complete response rate was below 25%. Results : Sixty consecutive patients (40F/20M) were included over a 21 months period. Mean age was 48 years (range 18–84). Mean ITP duration was 4.8 years. Mean platelet count at inclusion was 16±10x109/L. All but one patient, in whom reversible serum sickness disease was diagnosed after 2 infusions, received 4 infusions of rituximab. Fifteen other patients experienced transient side effects that did not lead to treatment discontinuation. No patient was lost to follow up. Success was achieved in 40 % (24/60 patients) (95 % confidence interval 28% to 52%) and was found significantly different from 25% (p=0.007). Among the 24 long term responders, platelet count at one year was ≥ 150x109/L in 18 and between 50 and 150 x109/L in 6. Two other patients (3%) had and incomplete response defined as a platelet count at one year between 30 and 50 x109/L but at least 2 fold the initial value. Thirty four (57%) patients failed to respond and amongst them, 18 have already undergone splenectomy. Conclusion: rituximab appears to be a safe and good splenectomy-sparing strategy in adults with chronic ITP leading to a significant and durable response in 40% of the cases.


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