a Phase II Study in Primary Central Nervous System Lymphoma

NCT00455286 | Unknown Phase 2 DMC

• 1 other identifier: T1406
• Study Type: interventional
• Target: 25
• Locations: 1 country
• Sites: 4

Brief Summary

In this study we will test the hypothesis that concurrent chemoradiation (CCRT) with temozolomide after induction chemotherapy by conventional high-dose methotrexate (HD-MTX) plus dexamethasone may be an effective and well tolerated treatment for immunocompetent patients with PCSNL. Corticosteroid can effectively reduce brain edema and corticosteroid alone has resulted in complete or partial remission in about 40% patients with PCNSL. To enhance local disease control, CCRT with temozolomide will be used in the study. Temozolomide is a well-tolerated oral alkylating agent that is able to permeate the BBB. Concurrent temozolomide with WBRT has shown superior effect to WBRT alone for the treatment of metastatic brain tumors and glioblastoma multiforme. In addition, temozolomide has single-agent activity for PCNSL (21% CR in relapsed or refractory PCNSL in a phase II trial). This is an open-label, non-randomized, multi-center phase II study. The primary end point of is the complete response rate. This study is a two-stage design for testing non-inferiority of the proposed treatment as compared to the approximately 80% response rate reported for conventional treatment. Assuming a non-inferiority margin of 20%, a sample size of 25 subjects, which provides an 80% power for establishment of non-inferiority. At the first stage, 15 subjects are to be enrolled. If equal to or more than 6 patients achieve complete response, the study would accrue additional 10 subjects. The treatment regimen is as follows. Induction chemotherapy: MS regimen (repeated every 14 days, total 4 cycles)

• Methotrexate 3.5 g/m2 i.v. infusion 4 hours on day1
• Methylprednisolone 200 mg/m2/day i.v. infusion 30 minutes, on day1-4 Concurrent chemoradiotherapy (CCRT)
• Whole brain radiation therapy (WBRT) 2 Gy per fraction daily, 5 days per week Temozolomide 75 mg/m2/day orally daily, only on the days of WBRT

Conditions

Primary Central Nervous System Lymphoma

Keywords

CNS Lymphoma

Outcome Measures

Primary Outcomes (2)

• Primary : To evaluate objective tumor response rate

• 

Secondary Outcomes (2)

• Secondary : To assess toxicity profile

• To assess time to disease progression

Interventions

Methotrexate DRUG

Methylprednisolone DRUG

Temozolomide DRUG

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must fulfill all the following criteria to be eligible for admission for the study:
• Histologically proven central nervous system lymphoma of brain parenchyma with or without leptomeningeal involvement.
• No evidence of systemic lymphoma.
• Age between 18 years and 75 years.
• With at least one measurable lesion, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as 10 mm. See Section 10.2.1 for the evaluation of measurable disease.
• Laboratory requirements :
• Hematology: Neutrophils≧ 1500/mm3, Hemoglobin≧ 10 g/dL, and Platelet count≧ 100000/mm3.
• Hepatic function: Total bilirubin level≦ 1.5x upper normal limit (UNL), ALT (SGPT) and AST (SGOT)≦ 2.5 x UNL.
• Renal function: Creatinine≦ 1.5 mg/dL.
• No prior malignancy (excluding in situ carcinoma of the cervix or non- melanomatous skin cancer) unless disease free for at least 5 years.
• Signed informed consent.
• Patients must be accessible for treatment and follow-up.

You may not qualify if:

• Patient meets any of the following will be excluded form the study.
• Patients who are seropositive for HIV, AIDS, use of immunosuppressant or who are post organ transplant are not eligible.
• Previously treated with chemotherapy, radiotherapy or other investigational agents. Patients with corticosteroid use are considered eligible.
• With ocular involvement or with any lesion beyond brain parenchyma except leptomeningeal.
• Pregnant, or lactating patients; patients of childbearing potential must implement adequate contractive measures during study participation.
• Other serious illness or medical conditions:
• Congestive heart failure or unstable angina pectoris. High risk uncontrolled arrhythmias.
• Uncontrolled infection (active serous infections that are not controlled by antibiotics.
• Concurrent treatment with any other experimental drugs.

Sponsors & Collaborators

• National Health Research Institutes, Taiwan: lead
• National Taiwan University Hospital: collaborator
• Mackay Memorial Hospital: collaborator
• China Medical University Hospital: collaborator
• National Cheng-Kung University Hospital: collaborator
• Chi Mei Medical Hospital: collaborator
• Taichung Veterans General Hospital: collaborator

Study Sites (4)

Changhua Christian Hospital

Changhua, Taiwan

RECRUITING

China Medical University Hospital

Taichung, Taiwan

RECRUITING

National Cheng Kung University Hospital

Tainan, Taiwan

RECRUITING

Mackay Memorial Hospital

Taipei, Taiwan

RECRUITING

MeSH Terms

Interventions

Methotrexate; Methylprednisolone; Temozolomide

Intervention Hierarchy (Ancestors)

Aminopterin; Pterins; Pteridines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds; Prednisolone; Pregnadienetriols; Pregnadienes; Pregnanes; Steroids; Fused-Ring Compounds; Polycyclic Compounds; Dacarbazine; Triazenes; Organic Chemicals; Imidazoles; Azoles; Heterocyclic Compounds, 1-Ring

Study Officials

• Ching-Hung Lin, M.D.

  National Taiwan University Hospital

  PRINCIPAL INVESTIGATOR

• Ann-Lii Cheng, Ph.D.

  National Taiwan University Hospital

  STUDY CHAIR

Central Study Contacts

Yueh-Ling Ho, RN

CONTACT

886-2-87923311; ylho@nhri.org.tw

Ching-Hung Lin, M.D.

CONTACT

886-2-2312-3456; dtmed004@ha.mc.ntu.edu.tw

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: April 2, 2007
• First Posted: April 3, 2007
• Study Start: November 1, 2006
• Study Completion: November 1, 2011
• Last Updated: April 4, 2007

Record last verified: 2007-04

Locations

TW (4)