Endostar Combined With CHOP Regimen as First Line Chemotherapy for Peripheral T Cell Lymphoma (PTCL)

Fudan University

Status and phase: Unknown; Phase 2

Conditions: T Cell Lymphoma

Treatments: Drug: endostar and CHOP

Study type: Interventional

Funder types: Other

Identifiers

NCT00974324

PTCL0908

Details and patient eligibility

About

The role of angiogenesis has been less clear in lymphoma than in solid tumors, in part related to the heterogeneity of disease and technical issues. In addition to vascular endothelial growth factor (VEGF) effects on angiogenesis and the integrity of tumor vasculature, autocrine VEGF-receptor (VEGF-R)-mediated signaling may play a role in lymphoma. Microvessel density, a measure of angiogenesis, is highest in peripheral T-cell lymphomas (PTCL), followed by diffuse large B-cell (DLBCL) and intra-follicular follicular lymphoma (FL).

Full description

To investigate efficacy and safety of endostar combined with CHOP regimen as first line treatment for peripheral T cell lymphoma.The second subject is to clarify the association between expression of VEGF and prognosis in peripheral T cell lymphoma,unspecified(PTCL-U) and angioimmunoblastic T-cellLymphoma(AILT).Methods 15 cases of PTCL were enrolled in this study.Immunohistochemical staining was performed by EnVision method using antibodies VEGF.

Enrollment: 15 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Disease Characteristics:

  • Diagnosis of peripheral T-cell:

    • Any stage disease allowed

  • At least 1 objective measurable disease parameter

  • No anaplastic lymphoma kinase (ALK)-positive T-cell large cell lymphoma

    • ALK-negative T-cell large cell lymphoma allowed

  • No cutaneous T-cell lymphoma

    • No sezary syndrome
    • No NK/T cell lymphoma

  • No history of or current radiographic evidence of CNS metastasis, including previously treated, resected, or asymptomatic brain lesions or leptomeningeal involvement

• Patient Characteristics:

  • Age:

    • 18 -75 years

  • Performance status:

    • ECOG 0-2

  • Life expectancy:

    • No less than 12 weeks

  • Hematopoietic:

    • Absolute neutrophil count ≥ 1,500/mm^3
    • Hemoglobulin ≥ 80*10^12/L
    • Platelet count ≥ 100,000/mm^3
    • No evidence of bleeding diathesis or coagulopathy

  • Hepatic:

    • Bilirubin ≤ 1.5 mg/dL
    • AST ≤ 2.5 times ULN
    • PT, INR, and PTT ≤ 1.5 times normal

  • Renal:

    • Creatinine ≤ 1.5 times normal

  • Cardiovascular:

    • No cerebrovascular accident within the past 6 months
    • No myocardial infarction within the past 6 months
    • No unstable angina within the past 6 months
    • No New York Heart Association class II-IV congestive heart failure
    • No uncontrolled hypertension (i.e., systolic blood pressure [BP] > 150 mm Hg or diastolic BP > 100 mm Hg)
    • No other clinically significant cardiovascular or peripheral vascular disease
    • LVEF is normal

  • Other:

    • Not pregnant or nursing
    • Fertile patients must use effective contraception
    • No history of active seizures
    • No non-healing ulcer (unless involved with lymphoma)
    • No active infection requiring parenteral antibiotics
    • No known HIV positivity
    • No other active malignancy within the past 6 months except carcinoma in situ of the cervix or basal cell carcinoma of the skin

• PRIOR CONCURRENT THERAPY:

  • Biologic therapy:

    • Not specified

  • Chemotherapy:

    • No prior chemotherapy was allowed

  • Surgery:

    • More than 4 weeks since prior major invasive surgery or open biopsy
    • At least 7 days since prior minor surgery
    • No concurrent major surgery

Exclusion criteria

• Prior treatment included chemotherapy and radiotherapy
• With the following risk factors: Uncontrolled or severe cardiovascular disease (e.g., myocardial infarction within the past 6 months, congestive heart failure treated with medications, or uncontrolled hypertension)
• Pregnant or nursing
• Other currently active malignancy except nonmelanoma skin cancer
• Uncontrolled or severe bleeding,diarrhea,intestinal obstruction
• Hypersensitivity to albumen

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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15 participants in 1 patient group

treatment

Experimental group

Description:

endostar combined with CHOP regimen

Treatment:

Drug: endostar and CHOP