Dolai Tuphan Kanti, Jain Manisha, Mahapatra Manoranjan
Department of Haematology, Nil Ratan Sircar Medical College and Hospital, Kolkata, India.
Department of Medical oncology and Haematology, Medanta Medcity, India.
Indian J Hematol Blood Transfus. 2023 Jul;39(3):357-370. doi: 10.1007/s12288-022-01592-4. Epub 2022 Oct 31.
Aplastic anemia (AA) is a rare immunologically mediated bone marrow failure syndrome, characterized by progressive loss of hematopoietic stem cells resulting in peripheral pancytopenia. Elaborative investigation including molecular tests is required to exclude inherited bone marrow failure syndrome (IMBFS) as the treatment and prognosis vary dramatically between them. Haematopoietic stem cell transplant with a fully matched sibling donor (MSD-HSCT) is still the only curative treatment. Management of AA is a real-time challenge in India, because of the delay in the diagnosis, lack of proper supportive care, limited availability of the expertise centre, and the patient's affordability. Recently, results with intensified immunosuppressive therapy that includes anti-thymocyte globulin with cyclosporine-A (CsA) and eltrombopag, are enough encouraging to consider it as treatment of choice in patients lacking MSD or who are not fit for HSCT. However, limitations in resource constraints settings including the cost of therapy limit its full utilization. Relapse of the disease or evolution to myelodysplasia or paroxysmal nocturnal haemoglobinuria (PNH) in a proportion of patients is another challenge with immunosuppressants. The majority of the AA patients still receive CsA with or without androgens in India, mostly because of increased cost and limited availability of HSCT and ATG. The use of the unrelated or alternative donor is still upcoming in India, with unavailable data in terms of response and survival. Therefore, there is an utmost need for novel agents for the better management of AA having a balanced efficacy and toxicity profile to improve the survival and quality of life.
再生障碍性贫血(AA)是一种罕见的免疫介导的骨髓衰竭综合征,其特征是造血干细胞逐渐丧失,导致外周血全血细胞减少。由于两者的治疗方法和预后差异很大,因此需要进行包括分子检测在内的详细调查,以排除遗传性骨髓衰竭综合征(IMBFS)。与完全匹配的同胞供体进行造血干细胞移植(MSD-HSCT)仍然是唯一的治愈性治疗方法。在印度,AA的管理是一项实时挑战,原因包括诊断延迟、缺乏适当的支持性护理、专业中心的可用性有限以及患者的经济承受能力。最近,包括抗胸腺细胞球蛋白与环孢素A(CsA)和艾曲泊帕在内的强化免疫抑制治疗结果令人鼓舞,足以将其视为缺乏MSD或不适合进行HSCT的患者的首选治疗方法。然而,包括治疗费用在内的资源限制环境中的局限性限制了其充分利用。一部分患者疾病复发或演变为骨髓增生异常综合征或阵发性夜间血红蛋白尿(PNH)是免疫抑制剂的另一个挑战。在印度,大多数AA患者仍接受CsA治疗,无论是否使用雄激素,主要是因为HSCT和ATG的成本增加且可用性有限。无关或替代供体的使用在印度仍处于起步阶段,关于反应和生存的数据不可用。因此,迫切需要新型药物来更好地管理AA,使其具有平衡的疗效和毒性特征,以提高生存率和生活质量。