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低剂量利妥昔单抗治疗慢性免疫性血小板减少症:在资源有限环境下仍是一种选择。

Low Dose Rituximab in Chronic ITP: Still an Option in Resource Limited Settings.

作者信息

Kapoor Rajan, Kumar Rajiv, Mahapatra M, Pati H P, Pramanik Suman Kumar

机构信息

Medicine and Clinical Hematology, Army Hospital (R&R), New Delhi, India.

Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Indian J Hematol Blood Transfus. 2017 Dec;33(4):568-573. doi: 10.1007/s12288-016-0764-x. Epub 2016 Dec 19.

Abstract

The etiology of ITP remains unknown but its pathogenesis consists of loss of tolerance to platelet antigens. There is a complex dysregulation of the immune system involving both the B cells and the T cells. Splenectomy is the standard second line option in steroid refractory chronic ITP patients. However, costs of surgery and reluctance for surgery in severely thrombocytopenic patients on part of surgeons are major obstacles in resource limited settings. Rituximab has been used in both the standard doses of 375 mg/m and low doses of 100 mg/m with similar results. We studied the utility of low dose Rituximab (@100 mg/m weekly × 4 doses) in resource limited settings. Overall response, complete response (CR) and partial response (PR) rates were 47.6% (10/21), 33.3% (7/21) and 14.3% (3/21) respectively. Median time to response in patients achieving CR was 75 days (range 45-185 days) while in patients achieving PR it was 105 days (range 45-165 days). However, there was no significant difference between males and females achieving CR or PR. We also observed that patients who had earlier responded to any form of treatment were more likely to respond to Rituximab treatment. The cumulative relapse free survival (RFS) at 13 months was 78%. By giving lower dose, six times less than conventional dosing dose, we have been able to demonstrate cost effectiveness in our study population. We were able to administer all the doses in day care without any major adverse events leading to further cost savings on in-patient care.

摘要

免疫性血小板减少症(ITP)的病因尚不清楚,但其发病机制包括对血小板抗原的耐受性丧失。免疫系统存在复杂的失调,涉及B细胞和T细胞。脾切除术是激素难治性慢性ITP患者的标准二线治疗选择。然而,在资源有限的环境中,手术费用以及部分外科医生对严重血小板减少症患者不愿进行手术是主要障碍。利妥昔单抗已用于375mg/m的标准剂量和100mg/m的低剂量,结果相似。我们研究了低剂量利妥昔单抗(每周100mg/m×4剂)在资源有限环境中的效用。总体缓解率、完全缓解(CR)率和部分缓解(PR)率分别为47.6%(10/21)、33.3%(7/21)和14.3%(3/21)。达到CR的患者中位缓解时间为75天(范围45 - 185天),而达到PR的患者为105天(范围45 - 165天)。然而,在达到CR或PR的男性和女性之间没有显著差异。我们还观察到,早期对任何形式治疗有反应的患者更有可能对利妥昔单抗治疗有反应。13个月时的累积无复发生存率(RFS)为78%。通过给予低剂量,比传统给药剂量少六倍,我们在研究人群中证明了成本效益。我们能够在日间护理中给予所有剂量,且没有任何导致住院护理进一步节省成本的重大不良事件。

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Can rituximab replace splenectomy in immune thrombocytopenic purpura?利妥昔单抗能否替代免疫性血小板减少性紫癜中的脾切除术?
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本文引用的文献

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Pathogenesis in immune thrombocytopenia: new insights.免疫性血小板减少症的发病机制:新见解。
Hematology Am Soc Hematol Educ Program. 2012;2012:306-12. doi: 10.1182/asheducation-2012.1.306.

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