Scheinberg Phillip, Finelli Carlo, Montaňo-Figueroa Efreen H, Vallejo Carlos, Norasetthada Lalita, Calado Rodrigo T, Turgut Mehmet, Peffault de Latour Régis, Kriemler-Krahn Ulrike, Haenig Jens, Clark Joan, Jang Junho
Division of Hematology, Hospital A Beneficência Portuguesa, São Paulo, Brazil.
Department of Oncology and Hematology, IRCCS Azienda Ospedaliero-Universitaria di Bologna Institute of Hematology Seràgnoli, Bologna, Italy.
Lancet Haematol. 2024 Mar;11(3):e206-e215. doi: 10.1016/S2352-3026(23)00395-2. Epub 2024 Feb 6.
Antithymocyte globulin (ATG)-based immunosuppression is standard in front-line treatment for people with severe aplastic anaemia without a histocompatible donor or who are 40 years or older. However, ATG requires in-hospital administration, is associated with infusion-related toxicities and has limited availability worldwide. In this study, we investigated the activity and safety of an ATG-free regimen of eltrombopag with cyclosporin A as a potential treatment for patients with severe aplastic anaemia who might not have access to or cannot tolerate horse-ATG.
SOAR was a multicentre, single-arm phase 2 trial investigating eltrombopag and cyclosporin in adult (≥18 years) patients with severe aplastic anaemia who were treatment-naive and had an Eastern Cooperative Oncology Group performance status of less than 2. Participants were recruited from 20 hospitals in ten countries. Eltrombopag was initiated at 150 mg (100 mg in patients of Asian ethnicity) and cyclosporin at 10 mg/kg per day (adjusted to a trough of 200-400 μg/L) orally from day 1 to 6 months. The primary outcome was an overall haematological response rate by 6 months in the intention-to-treat population. This is the final report of the primary analysis period. The trial was registered with ClinicalTrials.gov, NCT02998645, and has been completed.
54 patients were enrolled between May 11, 2017, and March 23, 2020. 34 (63%) patients were male and 20 (37%) were female. 22 (41%) were Asian, 22 (41%) were White, one (2%) was Native American or Alaska Native, one (2%) was Black or African American, and eight (15%) were other race or ethnicity. 35 patients (65%) completed 6 months of treatment with eltrombopag and cyclosporin and six (11%) completed the cyclosporin tapering period up to month 24. Overall haematological response rate by month 6 of treatment was 46% (25 of 54; 95% CI 33-60). The most reported adverse events were increased serum bilirubin (in 22 patients [41%]), nausea (16 [30%]), increased alanine aminotransferase concentration (12 [22%]), and diarrhoea (12 [22%]). Eight patients died on-treatment, but no deaths were considered related to the treatment.
Eltrombopag and cyclosporin was active as front-line treatment of severe aplastic anaemia, with no unexpected safety concerns. This approach might be beneficial where horse-ATG is not available or not tolerated.
Novartis Pharmaceuticals.
对于没有组织相容性供体或年龄在40岁及以上的重型再生障碍性贫血患者,基于抗胸腺细胞球蛋白(ATG)的免疫抑制是一线治疗的标准方案。然而,ATG需要住院给药,与输注相关的毒性有关,并且在全球范围内供应有限。在本研究中,我们调查了以艾曲泊帕与环孢素A组成的无ATG方案作为可能无法获得或不能耐受马ATG的重型再生障碍性贫血患者潜在治疗方法的活性和安全性。
SOAR是一项多中心、单臂2期试验,研究艾曲泊帕和环孢素在年龄≥18岁、初治且东部肿瘤协作组体能状态小于2的重型再生障碍性贫血成年患者中的应用。参与者从10个国家的20家医院招募。从第1天至6个月,艾曲泊帕起始剂量为150mg(亚洲种族患者为100mg),环孢素口服剂量为每日10mg/kg(调整至谷浓度为200 - 400μg/L)。主要结局是在意向性治疗人群中6个月时的总体血液学缓解率。这是主要分析期的最终报告。该试验已在ClinicalTrials.gov注册,编号为NCT02998645,现已完成。
2017年5月11日至2020年3月23日期间共纳入54例患者。34例(63%)为男性,20例(37%)为女性。22例(41%)为亚洲人,22例(41%)为白人,1例(2%)为美洲原住民或阿拉斯加原住民,1例(2%)为黑人或非裔美国人,8例(15%)为其他种族或族裔。35例患者(65%)完成了6个月的艾曲泊帕和环孢素治疗,6例(11%)完成了直至第24个月的环孢素减量期。治疗第6个月时的总体血液学缓解率为46%(54例中的25例;95%CI 33 - 60)。报告最多的不良事件是血清胆红素升高(22例患者[41%])、恶心(16例[30%])、丙氨酸转氨酶浓度升高(12例[22%])和腹泻(12例[22%])。8例患者在治疗期间死亡,但无死亡被认为与治疗相关。
艾曲泊帕和环孢素作为重型再生障碍性贫血的一线治疗有效,且无意外的安全问题。在无法获得或不能耐受马ATG的情况下,这种方法可能有益。
诺华制药公司。