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Effectiveness of Circulating DNA for Predicting the Relapse and Overall Survival in NHL Patients

Effectiveness of Circulating DNA for Predicting the Relapse and Overall Survival in Non-hodgkin Lymphoma Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03079947
Enrollment
300
Registered
2017-03-15
Start date
2017-01-31
Completion date
2020-01-31
Last updated
2017-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diffuse Large B Cell Lymphoma, Peripheral T Cell Lymphoma

Keywords

Circulating DNA, Diffuse Large B Cell Lymphoma, Peripheral T-Cell Lymphoma, prognosis

Brief summary

The purpose of this study is to evaluate the effectiveness of circulating DNA from peripheral blood for predicting the prognosis and relapse in DLBCL and PTCL patients.

Detailed description

The investigators plan to prospectively involve 300 Non-hodgkin Lymphoma patients, including both diffuse large B cell lymphomas and peripheral T cell lymphomas without previous treatment from Peking Union Medical College Hospital. The following parameters were collected: age, sex, subtype, Eastern Cooperative Oncology Group (ECOG) performance status (PS), Ann Arbor stage (I-IV), presence of B symptoms, number and type of involved sites, prognostic index including International Prognostic Index (IPI) for DLBCLand PIT for PTCL based on medical record review. All patients would have regular treatment and follow up in PUMCH. During the follow up, treatment response was evaluated by contrast enhanced computed tomography or PET-CT. The peripheral blood would be collected and circulating DNA would be tested at the time of diagnosis, interim of treatment, end of treatment, 1 year follow-up, 1.5 year of follow-up, 2 year of follow up, 3 year of follow-up and disease progression or relapse. TCR/BCR domain would be sequenced by high-throughput sequencing.

Interventions

None listed

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. pathologically confirmed diffuse large B cell lymphoma (DLBCL nos, PCNSL, ALK+ DLBCL, DLBCL/BL) or peripheral T cell lymphoma (AITL, ALCL, PTCL nos, NK/T nasal type, EATL, HSTL) 2. no treatment before 3. hCG(-) 4. 18 years old to 80 years old

Exclusion criteria

1. other tumors 2. severe infections

Design outcomes

Primary

MeasureTime frame
overall survival3 years

Secondary

MeasureTime frame
relapse of the diseasewithin 3 years
progression free survival3 years

Countries

China

Contacts

Primary ContactWei Zhang
vv1223@vip.sina.com86-010-69151235
Backup ContactXiao Han
xiaoer020@vip.sina.com+86 18618191308

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026