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NCT04957901Recruiting

The Value of Monitoring Circulating Cell DNA (ctDNA) in Pediatric Lymphoma: A Prospective, Multicenter Clinical Study

Source: ClinicalTrials.gov · Last updated 11 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The next-generation sequencing (NGS) based on liquid biopsy has been an emerging technology to identify tumor-specific genetic aberrations in malignant tumors. The tumor tissue (FFPE) and plasma samples from the newly diagnosed pediatric lymphoma patients were collected and sequenced by 475 genes panel before, during and post treatment, to evaluate the significance of the ctDNA in efficacy prediction, predicting recurrence or mechanism of resistance to chemotherapy for pediatric lymphoma.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
5 Jul 2021
Start date
1 Dec 2021
Primary completion date
1 Jun 2026
Lead sponsor
Sun Yat-sen University
NCT number
NCT04957901

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 1 Dec 2021 to the primary completion date, 1 Jun 2026
  • 1 site 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.

Other

  • Patients with any of the following items will not be enrolled in this study:
    • Incomplete baseline samples (preoperative plasma samples, tissue, bone marrow, cerebrospinal fluid) due to various reasons;
    • The follow-up samples cannot be obtained during the monitoring process;
    • The researcher considered it unsuitable for enrollment.

Who the study is looking for

  • Children with pediatric lymphoma (HL and NHL) that met the criteria and required treatment upon histological and pathological diagnosis;
  • Age: \< 18 years old;
  • The working status of the Eastern Cooperative Oncology Group (ECOG) (PS) : 0-2 points;
  • CT/MRI measurable lesion was defined as the longest diameter of at least 1 lymph node ≥ 1.5cm, and it was clearly measurable in 2 vertical directions;
  • Complete clinical laboratory examination and pathological examination information;
  • Patients can be evaluated on time, and the required samples can be obtained throughout the testing process;
  • After the patient is informed of the project, the informed consent signed by the patient or his legal representative is obtained.

Age in the registry: 1 year to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Yizhuo Zhang
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

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