跳至主要内容
临床试验/NCT05248256
NCT05248256已完成不适用

Vertebral Bone Marrow in Lung Cancer Attention Trial (VMAT)

The University of Texas Health Science Center at San Antonio4 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2022年9月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
4
主要终点
Limited G3L Toxicity

研究概览

简要总结

The purpose of this study is to see whether designing radiation to spare the vertebral bone marrow can limit the rates of lymphopenia during standard of care chemoradiation therapy and in the time to count recovery in the ensuing weeks. Secondary endpoints will examine whether this leads to improved disease control whether this is predictive of improved clinical outcomes such as rates of local recurrence (LR), metastasis free survival (MFS), overall survival (OS), and progression free survival (PFS) which will be followed prospectively up to 5 years.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patient > 18 years
  • Patients with AJCC (American Joint Committee on Cancer) 8 T1-T4, N1-N3, M0 stage IIIA-IIIC NSCLC (non small cell lung cancer)
  • Patients with oligometastatic disease stage IV, M1 disease, in which definitive concurrent chemoradiotherapy to the thorax is planned
  • CBC/CMP within these limits
  • Absolute lymphocyte count>500/ml
  • Hemoglobin>8 g/dL
  • AST (aspartate aminotransferase)/ALT (alanine transaminase) <2.5 times of ULN
  • Eastern Cooperative Oncology Group (ECOG) 0-2

排除标准

  • History of thoracic irradiation
  • History of palliative radiation for the current malignancy under consideration
  • Patients not being treated with definitive standard of care to the chest
  • History of bone marrow disease and or leukemia
  • History of prior cytotoxic chemotherapy for a disease other than for the current malignancy
  • Polymetastatic disease, defined here as ≥3 or more extrathoracic metastases
  • Administration of concurrent immunotherapy during radiation therapy, either as part of another clinical trial or otherwise

结局指标

主要结局

Limited G3L Toxicity

时间窗: 6 weeks

The primary end point will be evaluating whether implementing dosimetric constraints to the bone marrow will decrease rates of G3L toxicity in the peripheral blood compared to expected rates of 40% in large series examining toxicities during chemoradiation. Values will be expressed as a percentage rates of G3L lymphopenia.

次要结局

  • Progression free Survival (PFS)(Baseline to study end (up to 5 years))
  • Overall Survival (OS)(Baseline to study end (up to 5 years))
  • Change in Neutrophil to Lymphocyte ratio (NLR)(Baseline to study end (up to 5 years))
  • Local Recurrence (LR)(Baseline to study end (up to 5 years))
  • Metastasis Free Survival (MFS)(Baseline to study end (up to 5 years))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

Loading locations...

相似试验

Vertebral Marrow Attention Trial (VMAT) | 临床试验