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Study identifier: NCT05965557 Synced from ClinicalTrials.gov · July 29, 2026
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Exploration of Predictive Markers of Neoadjuvant Immunotherapy in Non-Small Cell Lung Cancer

Condition: Lung Cancer  ·  Sponsor: Geneplus-Beijing Co. Ltd.

PhaseN/A
Planned participants100
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Neoadjuvant immunotherapy has become the standard perioperative treatment in lung cancer, but its effective predictive biomarkers are lacking. A small cohort reported that homologous recombination deficiency (HRD) can be used as a reliable biomarker to predict the efficacy of neoadjuvant immunotherapy, but the findings need to be validated in larger cohorts. Moreover, circulating tumor DNA (ctDNA) has the potential to predict the therapeutic efficacy of neoadjuvant immunotherapy. This study intends to prospectively collect patients with driver-negative stage II-IIIB NSCLC who are scheduled to receive neoadjuvant immunotherapy and surgical resection and verify the value of HRD in predicting the efficacy of neoadjuvant immunotherapy. Meanwhile, the blood samples before and after neoadjuvant immunotherapy were collected for high-depth ctDNA detection to explore the correlation between the dynamic changes of ctDNA and the efficacy and prognosis of neoadjuvant immunotherapy.

This description comes directly from the study's public registry record.

Talk to the study team

Shun Lu, PhD  ·  +86 18017321551  ·  shunlu@sjtu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai Chest HospitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05965557