Primary Immune Thrombocytopenia and Thrombopoietin Receptor Agonists: Feasibilities of Treatment Discontinuation upon Achieving Stable Complete Platelet Response

Q4 Medicine
О. Ю. Виноградова, М. М. Панкрашкина, Анна Леонидовна Неверова, М. В. Черников, Л. А. Муха, Д. И. Шихбабаева, В. В. Птушкин
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 Materials & Methods. The study enrolled 456 patients with primary ITP who received second- and subsequent-line TPO-RA treatment. Complete platelet response (PR) was achieved in 338 patients, the therapy was discontinued in 116 of them. The present prospective clinical study started in 2014 and focused on the data of these 116 patients. Among them, there were 27 (23 %) men and 89 (77 %) women. By the time of TPO-RA therapy onset, the median age of the patients was 60 years (range 13–87 years), on ITP diagnosis date it was 52 years (range 1–80 years).
 Results. By the time of data analysis, 59 % of patients sustained PR after TPO-RA withdrawal. The median PR duration after TPO-RA withdrawal was 230 weeks. Romiplostim and eltrombopag recipients showed no significant differences in the survival rates without PR-loss after TPO-RA withdrawal. In the present study, the maximum PR duration achieved 9.5 years. The mid-term assessment of PR status was carried out in 3, 6, 12, 24, and 30 months after TPO-RA withdrawal and showed 99 %, 94 %, 83 %, 72 %, and 70 %, respectively. The number of previous therapy lines significantly affected the survival rates without PR-loss (p = 0.011). The age of patients, prior splenectomy, TPO-RA treatment duration, time to different PR levels on therapy, PR duration on TPO-RA therapy, and platelet count upon TPO-RA withdrawal showed no significant effect on this parameter. After PR-loss, TPO-RAs were administered again to 31 (27 %) patients. Repeated PR was achieved in 26 (84 %) of them.
 Conclusion. TPO-RA administration yields multi-year off-treatment remission in some patients with primary ITP. Upon therapy discontinuation, 59 % of patients with complete PR sustained PR for 3 months to 9.5 years. Stable PR after TPO-RA withdrawal significantly correlated with only one of the studied prognostic parameters, i.e., the number of previous therapy lines.","PeriodicalId":36905,"journal":{"name":"Klinicheskaya Onkogematologiya/Clinical Oncohematology","volume":"47 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Klinicheskaya Onkogematologiya/Clinical Oncohematology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21320/2500-2139-2023-16-4-413-425","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
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Abstract

Aim. To assess the stability of clinical remission in patients with primary immune thrombocytopenia (ITP) after withdrawal of thrombopoietin receptor agonists (TPO-RAs). Materials & Methods. The study enrolled 456 patients with primary ITP who received second- and subsequent-line TPO-RA treatment. Complete platelet response (PR) was achieved in 338 patients, the therapy was discontinued in 116 of them. The present prospective clinical study started in 2014 and focused on the data of these 116 patients. Among them, there were 27 (23 %) men and 89 (77 %) women. By the time of TPO-RA therapy onset, the median age of the patients was 60 years (range 13–87 years), on ITP diagnosis date it was 52 years (range 1–80 years). Results. By the time of data analysis, 59 % of patients sustained PR after TPO-RA withdrawal. The median PR duration after TPO-RA withdrawal was 230 weeks. Romiplostim and eltrombopag recipients showed no significant differences in the survival rates without PR-loss after TPO-RA withdrawal. In the present study, the maximum PR duration achieved 9.5 years. The mid-term assessment of PR status was carried out in 3, 6, 12, 24, and 30 months after TPO-RA withdrawal and showed 99 %, 94 %, 83 %, 72 %, and 70 %, respectively. The number of previous therapy lines significantly affected the survival rates without PR-loss (p = 0.011). The age of patients, prior splenectomy, TPO-RA treatment duration, time to different PR levels on therapy, PR duration on TPO-RA therapy, and platelet count upon TPO-RA withdrawal showed no significant effect on this parameter. After PR-loss, TPO-RAs were administered again to 31 (27 %) patients. Repeated PR was achieved in 26 (84 %) of them. Conclusion. TPO-RA administration yields multi-year off-treatment remission in some patients with primary ITP. Upon therapy discontinuation, 59 % of patients with complete PR sustained PR for 3 months to 9.5 years. Stable PR after TPO-RA withdrawal significantly correlated with only one of the studied prognostic parameters, i.e., the number of previous therapy lines.
原发性免疫性血小板减少症和血小板生成素受体激动剂:在达到稳定的完全血小板反应后停止治疗的可行性
的目标。评估原发性免疫性血小板减少症(ITP)患者停用血小板生成素受体激动剂(TPO-RAs)后临床缓解的稳定性。材料,方法。该研究纳入了456例接受二线和后续TPO-RA治疗的原发性ITP患者。338例患者达到完全血小板反应(PR),其中116例停止治疗。本前瞻性临床研究始于2014年,重点研究了这116例患者的数据。其中,男性27人(23%),女性89人(77%)。在TPO-RA治疗开始时,患者的中位年龄为60岁(范围13-87岁),在ITP诊断时,患者的中位年龄为52岁(范围1-80岁)。结果。截至数据分析时,59%的患者在TPO-RA停药后持续PR。TPO-RA停药后的中位PR持续时间为230周。Romiplostim和eltrombopag受体在TPO-RA停药后无pr损失的生存率无显著差异。在本研究中,PR最长持续时间达到9.5年。在TPO-RA停药后3、6、12、24、30个月进行PR状态中期评估,PR状态分别为99%、94%、83%、72%、70%。既往治疗线的数量显著影响无pr损失的生存率(p = 0.011)。患者年龄、既往脾切除术、TPO-RA治疗持续时间、治疗后达到不同PR水平的时间、TPO-RA治疗后PR持续时间、TPO-RA停药后血小板计数对该参数无显著影响。pr丢失后,31例(27%)患者再次接受TPO-RAs治疗。其中26例(84%)实现了重复PR。 结论。在一些原发性ITP患者中,给予TPO-RA可获得多年治疗后的缓解。在停止治疗后,59%的完全PR患者的PR持续了3个月至9.5年。TPO-RA停药后的稳定PR仅与所研究的预后参数中的一个显著相关,即既往治疗线的数量。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
20
审稿时长
12 weeks
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