跳至主要内容
临床试验/NL-OMON53375
NL-OMON53375尚未招募不适用

Adoptive TIL therapy in combination with chemoimmunotherapy in advanced NSCLC patients - TIL in NSCLC

eids Universitair Medisch Centrum0 个研究点目标入组 15 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
15

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

年龄范围
18 至 99(—)

入选标准

  • Age >=18 years
  • Presence of measurable stable or progressive disease according to RECIST
  • version 1.1.
  • Patients must have histologically confirmed metastatic NSCLC with at least
  • one lesion -primary or metastatic- of sufficient size (> 1 cm in total)
  • amendable for biopsy and/or resection and must be willing to undergo such a
  • procedure for experimental purposes. Furthermore there must be at least one
  • other lesion to monitor response.
  • Patients must have radiological stable disease on standard of care first line
  • treatment with at least two courses of single agent immunotherapy or
  • chemoimmunotherapy or progressive disease on or after standard of care first
  • line treatment.
  • In case the lung cancer is characterized by an oncogenic driver, patients
  • must have exhausted all targeted therapies and platinum based chemotherapy.
  • Patients must have a clinical performance status of ECOG 0 or 1 and an
  • expected life expectancy of at least 3 months.

排除标准

  • Requirement for immunosuppressive doses of systemic corticosteroids (>10
  • mg/day prednisone or equivalent) or other immunosuppressive drugs within the
  • last 3 weeks prior to start of treatment.
  • Patients who have uncontrolled central nervous system (CNS) metastases.
  • Patients who have asymptomatic CNS metastases no greater than 1 cm before
  • resection of a tumor lesion for retrieval of TIL may be eligible.
  • All toxicities due to prior non-systemic treatment must have recovered to a
  • grade 1 or less. Patients may have undergone minor surgical procedures or focal
  • palliative radiotherapy (to non-target lesions) within the past 4 weeks, as
  • long as all toxicities have recovered to grade 1 or less.
  • Serious acute or chronic illnesses, e.g. active infections requiring
  • antibiotics, bleeding disorders, or other conditions requiring concurrent
  • medications not allowed during this study.
  • Active immunodeficiency disease or autoimmune disease requiring immune
  • suppressive drugs. Vitiligo is not an exclusion criterion.

研究者

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