Clinical Application of Liquid Biopsy for Precise Diagnosis and Prognosis in Lymphoma

Sponsor
Ge Zheng (Other)
Overall Status
Completed
CT.gov ID
NCT04062877
Collaborator
(none)
60
1
42
1.4

Study Details

Study Description

Brief Summary

Lymphoma is a highly heterogeneous blood malignancy. It is very important to search for relative specific diagnostic markers that can detect related lymphoma in early stage for the treatment and long-term prognosis of the disease, as the hematopoietic diseases, such as lymphoma, are more difficult to biopsy than solid tumors, with more damage and side effects.Liquid Biopsy (Liquid Biopsy) refers to the extraction of solid biological tissue, is the most common blood, also including saliva, urine, cerebrospinal fluid and other body fluids, and extract the circulating tumor cells (circulating tumor cell, CTC) and circulating tumor DNA (circulating tumor DNA, ctDNA) is used to assess related diseases. CTCs/CSCs have the ability to generate new tumors and play a key role in tumor metastasis.This project intends to develop liquid biopsy technology for accurate diagnosis and prognosis judgment of lymphoma, to carry out clinical transformation application and serve patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    1. Patients with series and matched lymphoma who were refractory to initial diagnosis, remission and recurrence were enrolled, our research group will collected patient information comprehensively and signed the informed consent.

    2. The standard diagnosis process and treatment selection will be completed, and our research group willcollect relevant clinical and laboratory data.

    3. 5 ml of peripheral blood from each patient was collected with EDTA anticoagulant tube, and the blood cells were centrifuged at 820×g for 10 min at 4℃ within 1 h to separate the blood cells.The plasma was then transferred to a microcentrifuge tube and centrifuged at 4℃ at 20,000×g for 10 min to remove cell debris.According to the reagent instructions, cfDNA was extracted from 2 ml cell-free plasma and the concentration of cfDNA in each patient was determined.Meanwhile, genomic DNA kit was used to extract matching tumor DNA from lymphoma bone marrow tissue.

    4. We will extract the lymphoma of bone marrow tissue samples of RNA, and reverse transcription for cDNA, the use of qRT PCR verifying the mutations in tissue samples, after identifying the lymphoma five of the most common mutations from the cancer genome map (TCGA;http://cancergenome.nih.gov/) .

    5. The differences of mutations detected by liquid biopsy and tumor in situ biopsy will be compared, by NGS sequencing of peripheral blood cfDNA and lymphoma tissue DNA. Meanwhile, the mutation rate of each gene mutation was analyzed for lymphoma tissue type.

    6. The classification and malignant changes of matched lymphomas were statistically analyzed to study the differences in cfDNA concentration of different types of lymphomas, according to the cfDNA concentration determined at the earlier stage.

    7. The mutation differences of cfDNA in the peripheral blood of each patient will be compared at three time points before, during and after treatment, combined with PET/CT detection, and the correlation between cfDNA detection indexes and therapeutic effect and prognosis monitoring will be evaluated.

    8. SPSS 23.0 statistical software would be used to evaluate the correlation between cfDNA concentration in lymphoma and disease staging, grouping, subtype, efficacy prediction and recurrence monitoring. P<0.05 was considered statistically significant.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    60 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Clinical Transformation Application and Technology Research in Liquid Biopsy for Precise Diagnosis and Prognosis of Lymphoma
    Actual Study Start Date :
    Jul 1, 2018
    Actual Primary Completion Date :
    Dec 30, 2021
    Actual Study Completion Date :
    Dec 30, 2021

    Outcome Measures

    Primary Outcome Measures

    1. complete remission [From date of randomization or initial treatment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 weeks]

      Patients achieve complete remission after initial treatment

    2. relapse [From date of randomization or complete remission until the date of first documented relapse from any cause,assessed up to 100weeks.]

      Patients' disease progress after complete remission

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • patients of lymphoma diagnosed of de novo, CR, relapsed/refractory, be willing to receive treatment
    Exclusion Criteria:
    • leukemia

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Institute of Hematology Southeast University Department of Hematology Zhongda Hospital Southeast University Medical School NanJing Jiangsu China 210000

    Sponsors and Collaborators

    • Ge Zheng

    Investigators

    • Study Director: Zheng Ge, Director of Department of Hematology Zhongda Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ge Zheng, Director of Department of Hematology, Zhongda Hospital
    ClinicalTrials.gov Identifier:
    NCT04062877
    Other Study ID Numbers:
    • ZDYYGZ201907
    First Posted:
    Aug 20, 2019
    Last Update Posted:
    Mar 24, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ge Zheng, Director of Department of Hematology, Zhongda Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 24, 2022