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NCT05457049Recruiting

Adjuvant Therapy Omission for Resected NSCLC Patients With Longitudinal Undetectable MRD

Dynamic Observational Strategy for Stage IB-IIIA Non-Small Cell Lung Cancer Patients After Complete Resection Based on Longitudinal Undetectable Molecular Residual Disease: Prospective, Multicenter, Single-Arm Study

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

Molecular residual disease (MRD) has strong relationship with clinical outcome in multiple solid tumors. Here, the investigators try to verify the negative predictive value of undetectable MRD, which is considered as a superior prognostic factor for resected NSCLC patients, and not requiring excessive adjuvant therapy. Stage IB-IIIA resected NSCLC patients with landmark and longitudinal undetectable MRD are enrolled and under close surveillance in this study.

Status (registry)
Recruiting
Study type
Observational
Enrollment
180 (estimated)
First submitted
9 Jul 2022
Start date
1 Aug 2022
Primary completion date
31 Dec 2026
Lead sponsor
Guangdong Association of Clinical Trials
Diseases
Lung cancer
NCT number
NCT05457049

What you commit to

  • Study type: Observational
  • Planned participants: 180
  • From 1 Aug 2022 to the primary completion date, 31 Dec 2026
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who had previously undergone radiotherapy or chemotherapy or any other anti-tumor therapy.

Other illness

  • Patients with a history of other malignancies in the past 5 years.
  • Any unstable systemic disease (eg, active infection, high-risk hypertension, unstable angina, congestive heart failure, etc.).

Who the study is looking for

  • Stage IB-IIIA non-small cell cancer patients who after complete resection.
  • ≥18 years.
  • Two-round MRD tests confirm landmark undetectable MRD.
  • Expected survival ≥12 weeks.
  • Expected survival ≥12 weeks.
  • ECOG PS 1-2.
  • Willing to accept MRD monitoring every 3 months for a total of 2 years after operation.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First People's Hospital of Foshan
Coordinator of this site? Confirm its status
FoshanChinaRecruiting
Guangdong Lung Cancer Institute, Guangdong General Hospital, Guangdong Academy of Medical Sciences
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting
the First Affiliated Hospital of Shantou University Medical College
Coordinator of this site? Confirm its status
ShantouChinaRecruiting
Shantou Centeral Hospital
Coordinator of this site? Confirm its status
ShantouChinaRecruiting
Zhongshan City People's Hospital
Coordinator of this site? Confirm its status
ZhongshanChinaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.