RecruitingNot ApplicableNCT05040555

R-CDOP Regimen in the Treatment of Newly Diagnosed Non-Hodgkin's Lymphoma With High Tumor Burden

A Prospective Clinical Study of R-CDOP Regimen in the Treatment of Newly Diagnosed Non-Hodgkin's Lymphoma With High Tumor Burden


Sponsor

oubai, MD/PhD

Enrollment

64 participants

Start Date

Aug 30, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

A single-center, prospective clinical study to evaluate the efficacy and safety of R-CDOP (Rituximab, Cyclophosphamide, Doxorubicin hydrochloride liposome, Vindesine, Prednisone ) in the treatment of newly diagnosed high tumor burden non-Hodgkin's lymphoma, which has previously shown promising efficacy.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing a modified chemotherapy regimen called R-CDOP — which replaces one standard drug with a liposomal formulation to potentially reduce heart-related side effects — in patients with newly diagnosed diffuse large B-cell lymphoma or grade 3B follicular lymphoma with a large tumor burden. **You may be eligible if...** - You are between 18 and 75 years old with a confirmed diagnosis of diffuse large B-cell or grade 3B follicular lymphoma - Your lymphoma has high tumor burden (e.g., large tumors, multiple sites, high LDH, fluid buildup) - You have never been treated for this lymphoma before - Your performance status is ECOG 0–2 and organ function is adequate **You may NOT be eligible if...** - You have received prior treatment for this lymphoma - You have significant heart disease (heart failure, prior heart attack, severe valve disease) - You have active infections (including HIV, hepatitis B, C) - You are pregnant or breastfeeding - You have previously had severe allergic reactions to any of the study drugs Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

COMBINATION_PRODUCTR-CDOP

Rituximab 375mg/m2, D0; Cyclophosphamide 750mg/ m2, D1; Doxorubicin hydrochloride liposome 30-35mg/ m2, D1; Vindesine 3mg/ m2, D1; Prednisone 60mg/ m2, D1\~5.


Locations(1)

The First Bethune Hospital of Jilin University

Changchun, Jilin, China

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NCT05040555


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