Ganapiev A A, Golubovskaia I K, Zalialov Iu R, Estrina M A, Afanas'ev B V
Ter Arkh. 2010;82(7):48-52.
To evaluate the efficiency of related and unrelated allogeneic bone marrow transplantation (alloBMT) versus immunosuppressive therapy (IST) in patients with aplastic anemia (AA) having no HLA-compatible bone marrow donor.
The study covered 61 patients (34 men and 27 women) diagnosed as having acquired AA. Of them, 51 patients were diagnosed as having severe AA, 5 had supersevere AA, and 5 had non-severe AA. Combined IST (antithymocyte globulin (ATG) + cyclosporin A (CsA)) was used in 43 patients; allo-BMT was performed in 18. The basic types of ATG (ATGAM (Pfizer), thymoglobulin (Genzim), ATG (Fresenius), and goat antilymphocyte globulin (ALG) (Research Institute of Gerontology, Ministry of Health of the Russian Federation) were administered. CsA was given in a dose of 5 mg/kg/day. The standard conditioning regimen (ATGAM + cyclophosphanum) and fludarabine-containing (fludarabine + cyclophosphanum + ATG; busulfan + fludarabine + ATG) programs were used in the allo-BMT group. A combination of CsA and metothrexate was given to prevent a graft-versus-host reaction.
Among the IST-receiving patients, overall survival (OS) was 71%. After the first course of IST by follow-up month 6, the response rate was 74%. The second course of IST was performed in 7 patients unresponsive after the first-line IST and in 8 patients with recurrent AA. After the second course of IST, the response rate was 46.7%. Four patients who failed to achieve remission after 2 courses of IST received its third course. A complete response was obtained in 3 patients. In 18 patients following allo-BMT (related and unrelated), OS was 86%; event-free survival was 65. In 12 patients after related allo-BMT, OS was 91.7%.
Related allo-BMT is the method of choice if there is a HLA-compatible sibling. If there are contraindications to it or no related donor, IST with ATG + CsA is indicated. Ineffective IST is an indication for unrelated allo-BMT that may be recommended as life-saving therapy for young patients under 40 years of age.
评估在无人类白细胞抗原(HLA)相匹配骨髓供者的再生障碍性贫血(AA)患者中,相关和无关供者异基因骨髓移植(alloBMT)与免疫抑制治疗(IST)的疗效。
该研究纳入61例诊断为获得性AA的患者(34例男性和27例女性)。其中,51例诊断为重型AA,5例为极重型AA,5例为非重型AA。43例患者采用联合IST(抗胸腺细胞球蛋白(ATG)+环孢素A(CsA));18例患者接受allo - BMT。使用了ATG的基本类型(ATGAM(辉瑞公司)、胸腺球蛋白(基因公司)、ATG(费森尤斯公司)和山羊抗淋巴细胞球蛋白(ALG)(俄罗斯联邦卫生部老年医学研究所))。CsA的给药剂量为5mg/kg/天。allo - BMT组采用标准预处理方案(ATGAM + 环磷酰胺)和含氟达拉滨方案(氟达拉滨 + 环磷酰胺 + ATG;白消安 + 氟达拉滨 + ATG)。给予CsA和甲氨蝶呤联合用药以预防移植物抗宿主反应。
接受IST治疗的患者中,总生存率(OS)为71%。在IST的第一个疗程后至随访第6个月时,缓解率为74%。7例一线IST治疗无效的患者以及8例AA复发患者接受了第二个疗程的IST。第二个疗程的IST后,缓解率为46.7%。4例经过2个疗程IST仍未达到缓解的患者接受了第三个疗程的治疗。3例患者获得完全缓解。18例接受allo - BMT(相关和无关供者)的患者中,OS为86%;无事件生存率为65%。12例接受相关供者allo - BMT的患者中,OS为91.7%。
如果有HLA相匹配的同胞供者,相关供者allo - BMT是首选方法。如果存在其禁忌证或无相关供者,则推荐使用ATG + CsA进行IST。无效的IST是无关供者allo - BMT的指征,对于40岁以下的年轻患者,可将其作为挽救生命的治疗方法推荐。