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临床试验/NCT02997280
NCT02997280已完成2 期

Treatment of Steroid-refractory Acute and Chronic Graft-versus-host Disease With Inhibitor of Janus Kinases

St. Petersburg State Pavlov Medical University1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2016年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
75
试验地点
1
主要终点
Overall response rate

研究概览

简要总结

Steroid-refractory acute GVHD (srGVHD) is one of the causes of mortality after allogeneic stem cell transplantation, while steroid-refractory chronic GVHD significantly increases morbidity, aggravates quality of life and may also impact survival. Currently there is no standard treatment of srGVHD. One of the most promising agents is Janus kinase (JAK) inhibitor ruxolitinib, which in the retrospective study demonstrated excellent response rate and survival of patients with either acute or chronic srGVHD. This study prospectively evaluates the efficacy of ruxolitinib in srGVHD patients.

研究设计

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

入排标准

年龄范围
1 Year 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of graft-versus-host disease established based on tissue biopsy
  • Steroid-refractory acute or chronic graft-versus-host disease according to EBMT/ELN criteria (T. Ruutu et al, 2014)
  • Age 1 to 70 years
  • Karnofsky index >30%.
  • Ability for oral drug intake
  • Life expectancy > 1 month
  • Signed informed consent

排除标准

  • Severe organ dysfunction: AST or ALT >5 upper normal limits (excluding cases related to liver GVHD), creatinine >2 upper normal limits
  • Requirement for vasopressor support at the time of enrollment
  • Uncontrolled bacterial or fungal infection at the time of enrollment
  • Pregnancy
  • Somatic or psychiatric disorder making the patient (or legal guardian) unable to sign informed consent

研究组 & 干预措施

Ruxolitinib treatment

Experimental

Ruxolitinib 10 mg bid for adults and children with body weight > 40 kg, 0.15 mg/kg bid for children with body weight < 40 kg.

干预措施: Ruxolitinib Oral Tablet (Drug)

结局指标

主要结局

Overall response rate

时间窗: 84 days

Partial response for acute GVHD is defined as the improvement of at least one stage in the severity of aGVHD in one organ without deterioration in any other organ. A response had to last for at least 3 weeks. Partial response for chronic GVHD was defined as reduction in GVHD National Institute of Health (NIH) severity score at east for one organ without deterioration in any other organ. A complete response was defined as the absence of any symptoms related to GVHD. Overall response is defined as presence of partial or complete response

次要结局

  • 6-month overall survival(6 months)
  • Toxicity based NCI CTC grades(6 months)
  • Infectious complications, including analysis of severe bacterial, fungal and viral infections incidence(6 months)
  • GVHD relapse incidence after complete response(6 months)
  • Relapse incidence of underlying hematologic malignancy(12 months)
  • Quality of life measured by FACT BMT ver. 4 questionnaire in adults(6 months)
  • Quality of life measured by PedQL Stem Cell transplant module ver.1.0 questionnaire in children(6 months)

研究者

发起方
St. Petersburg State Pavlov Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ivan S Moiseev

Head of oncology, hematology and transplantation department for adults

St. Petersburg State Pavlov Medical University

研究点 (1)

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