Exposure to non-corticosteroid treatments in adult primary immune thrombocytopenia before the chronic phase in the era of thrombopoietin receptor agonists in France. A nationwide population-based study

2015 ◽  
Vol 14 (2) ◽  
pp. 168-173 ◽  
Author(s):  
Guillaume Moulis ◽  
Maryse Lapeyre-Mestre ◽  
Jean-Louis Montastruc ◽  
Laurent Sailler
Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 2178-2178
Author(s):  
Guillaume Moulis ◽  
Maryse Lapeyre-Mestre ◽  
Jean-Louis Montastruc ◽  
Bertrand Godeau ◽  
Laurent Sailler

Abstract Objectives:The aim of this study was to describe the exposure to corticoid-sparing treatments (CST) in adult primary immune thrombocytopenia (ITP) patients during the year before the chronic phase at a nationwide level in the era of thrombopoietin-receptor agonists (TPO-RAs). Methods:Study population was the 2009-2011 cohort of the French Adult Immune Thrombocytopenia: a French pHarmacoepidemiological study (FAITH, n°ENCEPP/SDPP/4574). The FAITH cohort is the cohort of all incident persistent or chronic adult primary ITP patients treated in France, built through the nationwide French health insurance database, named SNIIRAM. It collects prospectively all data regarding hospitalizations, disabling diseases, drug and procedure reimbursements. They are linkable with demographic data. On the 2009-2011 SNIIRAM data, ITP patients were identified with hospital and disabling disease diagnosis codes (D69.3 code of the International Classification of diseases, version-10). The date of diagnosis was refined thanks to out-hospital drug exposures. Secondary ITPs were excluded thanks to diagnosis codes of diseases associated to ITP, searched in the year before and the semester after the diagnosis. We restricted to incident patients, excluding those with a diagnosis during the first semester of the study, and then to patients followed at least 12 months and with at least one exposure to CST during the year after the diagnosis. Exposure to CST was searched through out-hospital dispensing, and during hospital stays for splenectomy, rituximab and polyvalent intravenous immunoglobulins (IVIg). A single dispensing defined exposure, except for IVIg (3 monthly dispensing were mandatory to differentiate IVIg used as CST from acute exposure to treat a serious bleeding). We described the percentage of patients exposed to the distinct CST at least once during the year after ITP diagnosis and detailed the lines of therapy. We compared the patients aged <65 years and those ≥65 years. Results:Out of 2334 adult incident primary ITPs, 1556 were persistent or chronic. Among them, 443 patients were followed at least one year after ITP diagnosis and were exposed to at least one CST during this period. Mean age was 52.7 ± 20.8 years and 59.1% of the patients were females. Patients aged ≥65 years had more frequently mucosal or internal bleeding at ITP onset, and had a higher Charlson’s comorbidity score. Mean time from diagnosis to CST was 3.5 months. CSTs used in >10% of the patients at any time during the year after ITP diagnosis were, by decreasing frequency: rituximab (57.8%), splenectomy (22.1%), TPO-RAs (16.8%), IVIg (15.0%), danazol (14.4%) and dapsone (10.8%). Hydroxychloroquine was used in 6.5% of the patients and immunosupressant (azathioprine, mycophenolate or ciclosporin) in 5.9%. The CST the most frequently used was rituximab in both age groups. Splenectomy was more frequently used in patients aged less than 65 years (25.2% versus 16.4%, p=0.03). In contrast, TPO-RAs and dapsone were more frequently used in patients aged over 65 years (respectively, 24.8% versus 12.8%, p=0.01, and 17.6% versus 7.2%, p=0.0008). The mean number of lines of therapy after corticosteroids was 1.5 (extremes: 1-6) and was not different between the two age groups. As regards CSTs used in second line after corticosteroids, rituximab was the most used (45.4%), followed by IVIg (12.0%), splenectomy (11.3%), danazol (10.1%), dapsone (7.9%) and TPO-RAs (6.3%). There were discrepancies according to the age groups: 11.8% of the patients aged ≥65 years had been exposed to TPO-RAs as second-line compared with 3.5% of younger patients (p=0.0006). Similarly, dapsone was more frequently used as second-line treatment in older patients (13.8% versus 5.2%, p=0.0003), while splenectomy was more frequently used in patients aged <65 years (13.8% versus 6.5%, p=0.02). When detailing the successive lines of therapy, the use of rituximab decreased, while the use of splenectomy and TPO-RA increased in both age groups. Conclusions: Rituximab was the leading CST used as second and third line of therapy in adult primary ITP before the chronic phase in France, whatever the age group. TPO-RAs have modified treatment strategy of persistent primary ITP as soon as they have been marketed. They were mainly used in accordance with their labeling (after two lines of treatment including corticosteroids). Disclosures No relevant conflicts of interest to declare.


Platelets ◽  
2016 ◽  
Vol 28 (5) ◽  
pp. 478-483 ◽  
Author(s):  
Sif Gudbrandsdottir ◽  
Waleed Ghanima ◽  
Claus H Nielsen ◽  
Xingmin Feng ◽  
Hans C Hasselbalch ◽  
...  

2021 ◽  
pp. 90-90
Author(s):  
Marijana Virijevic ◽  
Mirjana Mitrovic ◽  
Nikola Pantic ◽  
Zlatko Pravdic ◽  
Nikica Sabljic ◽  
...  

Background / Aim. The availability of thrombopoietin receptor agonists (TPO-RA) for the treatment of primary immune thrombocytopenia (ITP) over the last decade has transformed its management. The aim of this study was to assess the efficacy of TPO-RA in adults with chronic ITP treated in the University Clinical Centre of Serbia. Methods. A total of 28 adult ITP patients (10 males; 18 females) given eltrombopag and/or romiplostim were enrolled in the study. Data on demographic characteristics, ITP duration, previous therapeutic modalities, comorbidities, concomitant therapy, indications for TPO-RA, bleeding episodes, TPO-RA doses, adverse events and response rates were collected from the patients? medical records. TPO-RAs were administered: (a) in patients with chronic refractory ITP; (b) when splenectomy was contraindicated/unfeasible; (c) as preparation for splenectomy. A favourable treatment response was defined as a stable platelet count ? 50x109/L. Results. Twenty two (78.57%) and 14 (50.0%) subjects were treated with eltrombopag and romiplostim, respectively. A good treatment response (GTR) was achieved in 81.8% of the patients receiving eltrombopag and in 71.4% of those treated with romiplostim. The non-responders to eltrombopag (4 patients) and those who had lost their response to eltrombopag (4 patients) were switched to romiplostim. Six of them achieved a GTR. At the time of TPO-RA initiation, 46.4% of the patients used concomitant ITP therapy which was ceased in all those with a GTR. The following adverse effects of TPO-RA were registered: transaminitis and transient ischemic attack for eltrombopag - one patient each, and pulmonary embolism in one romiplostim treated patient. Conclusion. Our study showed that TPO-RAs are an effective and safe treatment option, since the majority of patients achieved stable remission without bleeding episodes.


2021 ◽  
Vol 12 ◽  
pp. 204062072110483
Author(s):  
Monica Carpenedo ◽  
Erminia Baldacci ◽  
Claudia Baratè ◽  
Alessandra Borchiellini ◽  
Francesco Buccisano ◽  
...  

Introduction: In patients with primary immune thrombocytopenia (ITP), a short course of steroids is routinely given as first-line therapy. However, the response is often transient and additional therapy is usually needed. Thrombopoietin receptor agonists (TPO-RAs) are frequently used as second-line therapy, although there is little clinical guidance on the timing of their administration and on tapering/discontinuation of the drug. To provide clinical recommendations, we used the Delphi technique to obtain consensus for statements regarding administration and on tapering/discontinuation of second-line TPO-RAs among a group of Italian clinicians with expertise in management of ITP. Methods: The Delphi process was used to obtain agreement on five statements regarding initiation and on tapering/discontinuation of second-line TPO-RAs. Agreement was considered when 75% of participants approved the statement. Eleven experts participated in the voting. Results: Full consensus was reached for three of the five statements. The experts held that an early switch from corticosteroids to a TPO-RA has the dual advantage of sparing patients from corticosteroid abuse and improve long-term clinical outcomes. All felt that dose reduction of TPO-RAs can be considered in patients with a stable response and platelet count >100 × 109/L that is maintained for at least 6 months in the absence of concomitant treatments, although there was less agreement in patients with a platelet count >50 × 109/L. Near consensus was reached regarding the statement that early treatment with a TPO-RA is associated with an increase in clinically significant partial or complete response. The experts also agreed that optimization of tapering and discontinuation of TPO-RA therapy in selected patients can improve the quality of life. Conclusion: The present consensus can help to provide guidance on use of TPO-RAs in daily practice in patients with ITP. Plain language summary Second-line administration of thrombopoietin receptor agonists in immune thrombocytopenia There is little guidance on the timing of administration and tapering/discontinuation of thrombopoietin receptor agonists (TPO-RAs) in patients with primary immune thrombocytopenia (ITP). The Delphi technique was used to obtain consensus for five statements. The present consensus among Italian clinicians aims to provide guidance on second-line use of TPO-RAs for patients with ITP in daily practice.


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