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临床试验/NCT05419843
NCT05419843尚未招募2 期

Up-front Matched Unrelated Donor Transplantation in Pediatric Patients With Idiopathic Aplastic Anemia: a Phase II Feasibility Study

Assistance Publique - Hôpitaux de Paris0 个研究点目标入组 25 人开始时间: 2022年6月最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
入组人数
25
主要终点
Proportion of patients with upfront matched unrelated donor (MUD) hematopoietic stem cell transplantation (HSCT) effectively performed

研究概览

简要总结

Pediatric patients with idiopathic aplastic anemia (AA) respond better than adults to immunosuppressive therapy (IST) but the long-term risks of relapse, ciclosporine dependence, and clonal evolution are high. UK investigators reported a 5-year estimated failure-free survival (FFS) after IST of 13.3%. In contrast, in 44 successive children who received a matched unrelated donor (MUD), hematopoietic stem cell transplantation (HSCT), there was an excellent estimated 5-year FFS of 95%. Forty of these children had previously failed IST. Because of those excellent results, up-front fully matched unrelated donor (MUD) hematopoietic stem cell transplantation (HSCT) became an attractive first-line option. In 2005 to 2014, a UK cohort of 29 children with idiopathic AA thus received MUD HSCTs as first-line therapy (they did not receive IST prior to HSCT). Results were excellent, with low Graft versus Host Disease rates and only 1 death (idiopathic pneumonia). This cohort was then compared with historical matched controls, transplanted or not. Outcomes for the up-front unrelated cohort HSCT were similar to Matched Related Donor HSCT and superior to IST and unrelated HSCT post-IST failure. Since then, many investigators are offering up-front MUD HSCT in pediatric patients worldwide. However, those results should be treated with extreme caution: 1) the design is retrospective; 2) the excellent up-front MUD HSCT may arise from the use of alemtuzumab in the conditioning regimen (alemtuzumab is not easily available worldwide) and 3) there was no formal quality-of-life assessment. Moreover, this strategy is highly dependent on donor identification (Caucasian patients have the highest likelihood of having a MUD) and donor not eventually receive HSCT because of the risk of infections/complications caused by unexpected donor delays or cancellation. Prospective trials are thus urgently needed to address the feasibility of such procedure, in term of timing (delay to offer MUD HSCT) and conditioning regimen (nothing is known of the use of other regimens, non alemtuzumab-based, in this setting).

The main objective of this Two-Stage Phase 2 multicenter study is to realize up-front HSCT within 2 months once a MUD has been identified.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • age<18years old
  • Pediatric patients aged less than 18 years with idiopathic aplastic anemia and an indication for treatment (severe aplastic anemia or moderate aplastic anemia requiring transfusions)
  • With a good probability to have a HLA-10/10 matched unrelated donor available (the patient needs to have at least 3 MUD identified within the book BMDW (Bone Marrow Donors Worldwide) or using the easy match software to be included)
  • With usual criteria for allo-SCT:
  • Lansky >70% for those below 16 years and Karnofsky > 70% for those above 16 years
  • No severe and uncontrolled infection
  • Adequate organ function: ASAT and ALAT ≤ 5N*, total bilirubin ≤ 2N, creatinine clearance > 70% of higher normal values for age.
  • With health insurance coverage
  • Contraception methods** for young girl and men of childbearing age must be prescribed during all the duration of the research.
  • Parents having read and understand the information note and signed a written informed consent (the patient's agreement depending on his age will be sought)
  • *because typical presentation of aplastic anemia post-hepatitis
  • ** NB : The authorized contraceptive methods are:
  • For women of childbearing age and in absence of permanent sterilization: oral, intravaginal or transdermal combined hormonal contraception, oral, injectable or transdermal progestogen-only hormonal contraception, intrauterine hormonal-releasing system (IUS).
  • For man in absence of permanent sterilization: condoms

排除标准

  • With a matched related donor available
  • With uncontrolled infection
  • With seropositivity for HIV or HTLV-1 or active hepatitis B or C defined by a positive PCR HBV or HCV and associated hepatic cytolysis
  • Renal failure with creatinine clearance below 70% of higher normal values for age
  • Pregnant (βHCG positive) or breast-feeding
  • With Heart failure according to NYHA (II or more)
  • Preexisting acute hemorrhagic cystitis
  • Urinary tract obstruction
  • Yellow fever vaccine within 2 months before transplantation
  • Who have any debilitating medical or psychiatric illness, which preclude understanding the inform consent as well as optimal treatment and follow-up (depending of his age and understanding).
  • With Contraindication to treatments used during the research

结局指标

主要结局

Proportion of patients with upfront matched unrelated donor (MUD) hematopoietic stem cell transplantation (HSCT) effectively performed

时间窗: within 2 months (60 days) after identification of a MUD

Proportion of patients with upfront matched unrelated donor (MUD) hematopoietic stem cell transplantation (HSCT) effectively performed in the first two months after unrelated donor search.

次要结局

  • Chronic GvHD incidence(at 24 months)
  • Relapse incidence(at 24 months)
  • Graft failure incidence(up to 24 months)
  • Progression free survival(at 24 months)
  • Neutrophils engraftment(at day 100)
  • Platelets engraftment(at day 100)
  • Incidence of EBV infection(at 12 months)
  • Immune reconstitution(at 24 months)
  • Acute GvHD incidence(at month 3)
  • Proportion of patients with a donor chimerism of 90% or more(at 12 months)
  • Ferritin levels(at 24 months)
  • Absolute number of neutrophils(at day of last platelet and red blood cell transfusions (assessed up to 24 months))
  • Absolute numbers of platelets(up to 24 months)
  • Incidence of CMV infection(at 12 months)
  • Non-relapse mortality(at 24 months)
  • Quality of life questionnaires PedsQL(at 24 months)
  • Incidence of severe infections(at 24 months)
  • Overall survival(at 24 months)

研究者

申办方类型
Other
责任方
Sponsor

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