跳至主要内容
临床试验/ISRCTN86739591
ISRCTN86739591进行中(未招募)3 期

PETReA: Phase 3 evaluation of PET-guided, Response-Adapted therapy in patients with previously untreated, high tumour burden follicular lymphoma

niversity of Liverpool0 个研究点目标入组 840 人开始时间: 2018年8月13日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
840

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Must be =18 years of age at the time of signing the informed consent form
  • 2. Must be able to adhere to the study visit schedule and other protocol requirements
  • 3. Must have a documented diagnosis of follicular lymphoma (grade 1, 2 or 3a)
  • 4. Must be at non-contiguous stage II, stage III or stage IV
  • 5. Must fulfil at least one of the Groupe d'Etude des Lymphomas Folliculaires (GELF) GELF criteria for high tumour burden:
  • 5.1. Systemic symptoms (> 10% weight loss, temperature = 38°C for more than 5 days, abundant night sweats)
  • 5.2. Performance status (PS) greater than 1 according to the Eastern Cooperative Oncology Group (ECOG) scale
  • 5.3. Elevated lactate dehydrogenase (LDH) level
  • 5.4. ß2-microglobulin level greater than 25.5 nM/L (3 µg/mL)
  • 5.5. A single lymph node larger than 7 cm
  • 5.6. Involvement of at least 3 nodal sites, each with diameter greater than 3 cm
  • 5.7. Marked splenomegaly
  • 5.8. Organ failure
  • 5.9. Pleural effusion or ascites
  • 5.10. Orbital or epidural involvement
  • 5.11. Blood infiltration
  • 5.12. Cytopenia
  • 6. Must not have received prior systemic therapy (local radiotherapy is permitted)
  • 7. Must have a WHO performance status score of less than or equal to 2
  • 8. Must agree to adhere to the Celgene guidance on pregnancy prevention

排除标准

  • 1. Any serious medical condition that would prevent the subject from participating in the study
  • 2. Known active infection with HIV, HBV or HCV
  • 3. Pregnant or lactating females
  • 4. Central nervous system involvement as documented by spinal fluid cytology or imaging
  • 5. History of active malignancy during the past 5 years with the exception of basal carcinoma of the skin, squamous cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, prostate cancer (TNM stage of T1a or T1b)
  • 6. Any of the following laboratory abnormalities:
  • 6.1. Absolute neutrophil count (ANC) < 1,000/µL (1.0 X 109/L)
  • 6.2. Platelet count < 50,000/µL (50 X 109/L)
  • 6.3. Serum alanine transaminase (ALT) > 3.0 x upper limit of normal (ULN)
  • 6.4. Serum total bilirubin > 1.5 x ULN unless due to Gilbert's Syndrome or biliary obstruction by lymphoma

研究者

发起方
niversity of Liverpool

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