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NCT Number: NCT05040555

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

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.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Bethune Hospital of Jilin University

Changchun, Jilin, 130021, China

Location status: Recruiting

Location contact

Ou BAI, doctor

CONTACT

[email protected]

13039046656

About this study

The objective was to evaluate the efficacy and safety of R-CDOP regimen in the initial treatment of Patients with at least one of the following high tumor burden, and to provide a basis for the application of Doxorubicin hydrochloride liposome.

At least 3 nodal sites (each with a diameter greater than 3 cm) ; Nodal or extranodal mass > 7cm in its greater diameter; Hepatomegaly and splenomegaly (infiltration confirmed by PET-CT; Spleen: female > 15cm, male > 16cm) ; Pleural/peritoneal effusion; Lactate dehydrogenase (LDH) three times the upper limit of normal; PET-CT Total Metabolic Tumor Volume (TMTV)>220cm3.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically immunohistochemistry and imaging confirmed diffuse large B-cell lymphoma or follicular lymphoma grade 3B;
  • Has at least one evaluable or measurable lesion according to Lugano response criteria;
  • Patients with at least one of the following high tumor burden Involvement of at least 3 nodal sites (each with a diameter greater than 3 cm); nodal or extranodal mass > 7cm in its greater diameter; Hepatomegaly and splenomegaly (infiltration confirmed by PET-CT; Spleen: female > 15cm, male > 16cm); Pleural/peritoneal effusion; Lactate dehydrogenase (LDH) three times the upper limit of normal; PET-CT TMTV >220cm3;
  • Patients previously untreated;
  • Patients aged over 18 and under 75 years;
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0~2;
  • International Prognostic Index (IPI) score > 1, or with extranodal mass diameter ≥7cm;
  • Life expectancy ≥ 6 months;
  • Left Ventricular Ejection Fraction (LVEF) ≥ 50%;
  • Patients must sign informed consent and be willing and able to comply with the requirements of visits, treatment, laboratory tests and other research requirements stipulated in the research schedule.

Exclusion criteria

  • Pregnant or lactation and patients of childbearing age who do not want to take contraceptive measures;
  • Abnormal liver function [total bilirubin > 1.5 times of the upper limit of normal value; Alanine aminotransferase/Aspartate aminotransferase (ALT / AST) > 2.5 times of upper limit of normal value for patients without liver metastasis ; ALT / AST > 5 times of upper limit of normal value for patients with liver metastasis ], abnormal renal function (serum creatinine > 1.5 times of upper limit of normal value) ;
  • Absolute Neutrophil Count (ANC)<1.5×10^9/L or Platelet (PLT)< 75 × 10^9/L;
  • Hypersensitivity to any study drug or its ingredients;
  • Patients with significant and uncontrolled cardiovascular disease or history;
  • Persons with mental disorders/unable to obtain informed consent;
  • Lymphoma infiltrates the central nervous system;
  • Previous history of malignant tumor;
  • HIV infection; HBV infection (HBV-DNA> 2000 IU/ml);HCV infection (HCV-RNA>200 IU/ml);
  • The investigator determined not suitable to participate in this study.

Treatment and study plan

R-CDOP

Combination Product

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

Primary outcomes

  1. Objective response rate

    Time frame: 24 months

    Percentage of Complete remission (CR), and Partial remission (PR), referred to Lugano 2014.

Secondary outcomes

  1. Disease Control Rate

    Time frame: 24 months

    Percentage of Complete remission (CR), Partial remission (PR), and stable disease (SD), referred to Lugano 2014.

  2. Progression-free survival

    Time frame: 24 months

    Progression-free survival(PFS) is defined as the time from the date of enrollment to the date of first documentation of progressive disease (PD) or death from any cause.

  3. Overall survival

    Time frame: 60 months

    Overall survival(OS) is defined as the time from the date of enrollment to the date of death from any cause.

  4. Adverse Events

    Time frame: 24 months

    An adverse event is any untoward medical occurrence in a participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with the treatment. An adverse event can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a pharmaceutical product, whether or not considered related to the pharmaceutical product. Preexisting conditions which worsen during a study are also considered as adverse events.

Study contacts

Contact information is provided by the study sponsor or research team.

Ou BAI, doctor

CONTACT

[email protected]

13039046656

Sponsors and collaborators

Lead sponsor

oubai, MD/PhD

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2023
Study completion
2028
First posted
Sep 10, 2021
Registry last updated
Sep 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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