再生障碍性贫血免疫抑制治疗的长期结果:单中心经验

Елена Романовна Шилова, Н. А. Романенко, Д. А. Чебыкина, Т. В. Глазанова, М. Н. Зенина, И. Е. Павлова, С. С. Бессмельцев
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 Materials & Methods. The study enrolled 30 AA patients who received IST for more than 5 years (continuous follow-up of 5.5–33 years) with monitoring of the main hemogram parameters and PNH clone size. Patients were aged 19–73 years (median 29 years). There were 8 women and 12 men. Based on international criteria, severe AA (SAA) was initially diagnosed in 18 patients, and non-severe АА (NAA) was diagnosed in 12 patients. Combined IST was administered to 22 patients (18 SAA patients and 4 NAA patients), the remaining 8 patients received ATG (n = 1) and CsA (n = 7).
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引用次数: 0

摘要

背景。骨髓移植不符合条件的再生障碍性贫血(AA)最有效的治疗方法是联合免疫抑制疗法(IST)。大多数患者的病情得到缓解。但存在复发频繁、血液学恢复不完全、有克隆进化风险等缺点。此外,АА并不总是按照标准方案治疗。由于不同的原因,一些AA患者接受延迟治疗或IST单药治疗,主要是环孢素A (CsA)。的目标。评估在俄罗斯血液学和输血研究所治疗开始后随访5年的AA患者的长期IST结局。 材料,方法。本研究纳入30例接受IST治疗5年以上的AA患者(连续随访5.5-33年),同时监测主要血流图参数和PNH克隆大小。患者年龄19-73岁(中位年龄29岁)。有8个女人和12个男人。根据国际标准,18例患者最初被诊断为重度AA (SAA), 12例患者被诊断为非重度АА (NAA)。22例患者接受联合IST治疗(SAA患者18例,NAA患者4例),其余8例患者接受ATG (n = 1)和CsA (n = 7)。 结果。30例患者中有28例(93.3%)对IST有反应,其中16例(53.3%)完全缓解。本文记录了4例缓解期女性患者的血液学恢复特点,取决于标准治疗方案的依从性,以及疾病变异、晚期并发症的发展和克隆进化、妊娠和分娩特征。超过一半(16名患者中有10名)的PNH克隆增加。2.6%。在2例(6.7%)AA完全缓解的患者中,长期克隆进化为髓系肿瘤(IST发病13年后)。无菌性(无血管性)骨坏死为并发症,随访6例(20%)。结论。该研究的结果强调了早期开始和坚持标准联合IST方案的重要性和必要性,旨在SAA和NAA患者获得最佳治疗效果,以及完成IST后患者的长期随访。
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Long-Term Outcomes of Immunosuppressive Therapy for Aplastic Anemia: A Single-Center Experience
Background. Bone marrow transplantation-ineligible aplastic anemia (AA) is most effectively treated with combined immunosuppressive therapy (IST). It yields remissions in most patients. However, it has such disadvantages as frequent relapses, incomplete hematologic recovery, and clonal evolution risk. Besides, АА is not always treated according to standard regimens. For different reasons, some AA patients receive delayed therapy or IST mono-treatment predominantly with cyclosporine A (CsA). Aim. To assess long-term IST outcomes in AA patients followed-up at the Russian Research Institute of Hematology and Transfusiology for 5 years after therapy onset. Materials & Methods. The study enrolled 30 AA patients who received IST for more than 5 years (continuous follow-up of 5.5–33 years) with monitoring of the main hemogram parameters and PNH clone size. Patients were aged 19–73 years (median 29 years). There were 8 women and 12 men. Based on international criteria, severe AA (SAA) was initially diagnosed in 18 patients, and non-severe АА (NAA) was diagnosed in 12 patients. Combined IST was administered to 22 patients (18 SAA patients and 4 NAA patients), the remaining 8 patients received ATG (n = 1) and CsA (n = 7). Results. A response to IST was achieved in 28 (93.3 %) out of 30 patients, 16 (53.3 %) of them showed complete remission. This paper documents the characteristics of hematologic recovery depending on the compliance with standard therapy regimens, as well as on the disease variant, development of late complications and clonal evolution, characteristics of pregnancy and childbirth in 4 female patients in remission. PNH clone increased in more than a half (10 out of 16) patients whose clone was initially > 2.6 %. Long-term clonal evolution to myeloid neoplasia (13 years after IST onset) was registered in 2 (6.7 %) patients with complete AA remission. Aseptic (avascular) osteonecrosis as complication was reported in 6 (20 %) followed-up patients. Conclusion. The results of the study highlight the importance of and the need for early start and adherence to standard combined IST regimens aimed at optimum therapeutic effect in both SAA and NAA patients, as well as for long-term follow-up of patients after completing IST.
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