Skip to content

The clinical study on the efficacy and safety of CDOP regimen with pegylated liposomal doxorubicin ± rituximab in the treatment of diffuse large B-cell lymphoma

The clinical study on the efficacy and safety of CDOP regimen with pegylated liposomal doxorubicin ± rituximab in the treatment of diffuse large B-cell lymphoma

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800020142
Enrollment
Unknown
Registered
2018-12-17
Start date
2013-05-27
Completion date
Unknown
Last updated
2019-01-14

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

Interventions

case series:PLD 25 mg/ m2,iv,d1,cyclophosphamide 750 mg/m2, vincristine 1.4 mg/m2, up to 2 mg, or vindesine 3 mg/m2, intravenously (iv.) all on day 1
and prednisone 100 mg orally on days 1 to 5, with or without rituximab 375 mg/m2, iv. on day 0, administered every 21 days (n=304) for six or eight cycle

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The enrolled patients were histopathologically definitively diagnosed with DLBCL, aged 60 or older, or aged 18-60 with arrhythmia, coronary heart disease, abnormal heart function (identified by the New York Heart Association [NYHA] as Grade I), or hypertension but well controlled. Other inclusion criteria included objectively measurable tumor lesions, ECOG score = 2 points, expected survival > 3 months, normal blood, liver and kidney function, and LVEF = 50%.

Exclusion criteria

Exclusion criteria: 1) Patients with grade II or higher heart disease identified based on the NYHA score; 2) Invasion of the central nervous system; 3) Other malignancies in the past 5 years, except cervical carcinoma in situ or non-malignant melanoma skin cancer; 4) Pregnancy or breastfeeding women and patients of childbearing age who refuse to adopt appropriate contraceptive measures during treatment; 5) Participating in other clinical researches at the same time.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
Progression?Free?Survival;Cardiac toxicity;the incidence of adverse events;

Countries

China

Contacts

Public ContactZhu Jun

Beijing Cancer Hospital

zhujun@csco.org.cn+86 010 88196116

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026