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Multi Dimensional Precise Exploration of Immunoconsolidation Therapy for Locally Advanced NSCLC After Chemo-radiotherapy

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Fudan University

Status

Unknown

Conditions

ctDNA
Chemoradiotherapy
NSCLC

Study type

Observational

Funder types

Other

Identifiers

NCT04741633
CID-001

Details and patient eligibility

About

The purpose of this study is to carry out a prospective observational study in patients with locally advanced NSCLC receiving radical concurrent chemoradiotherapy and follow-up immune consolidation therapy. By detecting ctDNA and TILs of the patients, we explored the value of blood dynamic monitoring of ctDNA in patients with prognosis stratification and treatment effect, and explored the patients before and after concurrent chemoradiotherapy and immune consolidation therapy The characteristics of DNA, RNA, T cells and other biomarkers were correlated with the efficacy and prognosis.

Enrollment

25 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Non small cell lung cancer patients confirmed by pathology;
  2. They were 18-80 years old;
  3. The tumor could not be resected or could not tolerate surgery;
  4. Planed to receive chemoradiotherapy and subsequent immunoconsolidation therapy;
  5. Clinical stage III (AJCC, 8th Edition, 2017);
  6. After systematic detection of non-small cell lung cancer core indicators including EGFR, ALK, ros1, KRAS, ntrk, TMB, etc;
  7. Patient informed consent.

Exclusion criteria

  1. After radiotherapy and chemotherapy, the disease progressed and immune maintenance therapy could not be carried out
  2. It can not cooperate with the completion of baseline mutation screening and subsequent sample detection
  3. Factors judged by other researchers not suitable for further study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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