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Thalidomide-based regimen shows promising efficacy in large granular lymphocytic leukemia: a multicenter phase II study.

Ying Yu | Yuxi Li | Rui Cui | Yuting Yan | Fei Li | Yan Chen | Tingyu Wang | Xiaoli Hu | Yaqing Feng | Tengteng Yu | Yanshan Huang | Jingwen Sun | Rui Lyu | Wenjie Xiong | Qi Wang | Wei Liu | Gang An | Weiwei Sui | Yan Xu | Wenyang Huang | Dehui Zou | Huijun Wang | Zhijian Xiao | Jianxiang Wang | Lugui Qiu | Shuhua Yi
Signal transduction and targeted therapy | 2025

Large granular lymphocytic leukemia (LGLL) is characterized by the clonal proliferation of cytotoxic T lymphocytes or NK cells. Standard first-line immunosuppressive treatments have limitations, achieving complete remission (CR) rates of up to 50%. Immune system dysregulation is implicated in LGLL. Promising results for thalidomide, an immunomodulatory drug, combined with prednisone and methotrexate (TPM), were observed in our pilot study. This multicenter study evaluated the efficacy and safety of a thalidomide, prednisone, and methotrexate (TPM) regimen in 52 symptomatic, methotrexate- and thalidomide-naive LGLL patients from June 2020 to August 2022. Thalidomide (100 mg daily for up to 24 months), prednisone (0.5-1.0 mg/kg every other day, tapered after 3 months), and methotrexate (10 mg/m2 weekly for up to 12 months) were administered. The primary objective was to determine the CR rate. The median follow-up duration was 29.0 months (range: 4.0-42.0). Forty-seven patients (90.4%) achieved hematological and symptomatic responses. Thirty-nine patients (75.0%) achieved CR. The median time to response was 3.0 months (range: 3.0-9.0). The median progression-free survival was 40.0 months (95% confidence interval (CI): 38.0-42.0), and the median duration of response was 39.0 months (95% CI: 36.1-41.9). The most common adverse event was peripheral neuropathy (24.1%), most of which (84.6%) were grades 1-2. Four patients experienced grade ≥3 adverse events. In conclusion, the TPM regimen was an effective and safe treatment for symptomatic LGLL patients, with a particularly high CR rate. This trial was registered at www.clinicaltrials.gov (#NCT04453345).

Pubmed ID: 40069155

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Associated grants

  • Agency: National Natural Science Foundation of China (National Science Foundation of China),
    Id: 82170193
  • Agency: National Natural Science Foundation of China (National Science Foundation of China),
    Id: 82200215
  • Agency: National Natural Science Foundation of China (National Science Foundation of China),
    Id: 82370197
  • Agency: Chinese Academy of Medical Sciences (CAMS),
    Id: 2021-I2M-C&T-B-08
  • Agency: Chinese Academy of Medical Sciences (CAMS),
    Id: 2022-I2M-1-022

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ClinicalTrials.gov (tool)

RRID:SCR_002309

Registry and results database of federally and privately supported clinical trials conducted in United States and around world. Provides information about purpose of trial, who may participate, locations, and phone numbers for more details. This information should be used in conjunction with advice from health care professionals.Offers information for locating federally and privately supported clinical trials for wide range of diseases and conditions. Research study in human volunteers to answer specific health questions. Interventional trials determine whether experimental treatments or new ways of using known therapies are safe and effective under controlled environments. Observational trials address health issues in large groups of people or populations in natural settings. ClinicalTrials.gov contains trials sponsored by National Institutes of Health, other federal agencies, and private industry. Studies listed in database are conducted in all 50 States and in 178 countries.

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