Choi Philip Young-Ill, Roncolato Fernando, Badoux Xavier, Ramanathan Sundra, Ho Shir-Jing, Chong Beng H
St George Clinical School, University of New South Wales, Kogarah, NSW, Australia; and.
Department of Haematology, St George Hospital, Kogarah, NSW, Australia.
Blood. 2015 Jul 23;126(4):500-3. doi: 10.1182/blood-2015-03-631937. Epub 2015 May 13.
Promising reports of combination immunosuppression with high-dose dexamethasone and rituximab for the treatment of primary immune thrombocytopenia (ITP) have recently emerged. They suggest a potential to further optimize the efficacy of therapy. We investigate the use of a novel combination of conventional therapies in ITP given over 4 weeks. From 2011 to 2014, 20 patients were prospectively enrolled onto a single-arm phase 2b study to describe the safety, efficacy, and tolerability of oral dexamethasone 40 mg for days 1 to 4, oral cyclosporine 2.5 to 3 mg/kg daily for day 1 to 28, and intravenous low-dose rituximab 100 mg for days 7, 14, 21, and 28. There were no therapy-related serious adverse side effects, 6-month response rate was 60%, and treatment was well tolerated. Responders enjoyed relapse-free survivals of 92% and 76%, respectively, at 12 and 24 months. This study highlights the possibility of achieving an enduring remission from 4 weeks of therapy. This study is registered at www.anzctr.org.au (#ANZCTRN12611000015943).
最近出现了关于高剂量地塞米松与利妥昔单抗联合免疫抑制治疗原发性免疫性血小板减少症(ITP)的有前景的报道。这些报道表明进一步优化治疗效果具有潜力。我们研究了在4周内给予ITP患者一种新型传统疗法组合的应用情况。2011年至2014年,20例患者前瞻性纳入一项单臂2b期研究,以描述第1至4天口服40mg地塞米松、第1至28天每日口服2.5至3mg/kg环孢素以及第7、14、21和28天静脉注射100mg低剂量利妥昔单抗的安全性、疗效和耐受性。未出现与治疗相关的严重不良副作用,6个月缓解率为60%,且治疗耐受性良好。缓解者在12个月和