Overview

Molecular Risk Assessment in Planning Treatment for Patients With Non-Hodgkin's Lymphoma

Status:
Completed
Trial end date:
2006-03-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Analyzing genes that are present in cancer cells may be useful as a method for predicting the response of non-Hodgkin's lymphoma to cancer treatment. Imaging procedures such as positron emission tomography (PET) scans may improve the ability to measure how well cancer has responded to treatment. PURPOSE: This phase II trial is studying molecular risk assessment to see how well it works in predicting response to therapy in patients who are receiving treatment for non-Hodgkin's lymphoma.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Case Comprehensive Cancer Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Cyclophosphamide
Doxorubicin
Liposomal doxorubicin
Prednisone
Rituximab
Vincristine
Criteria
DISEASE CHARACTERISTICS:

- Histologically confirmed diffuse large B-cell non-Hodgkin's lymphoma

- CD20 and/or CD19 positive by immunohistochemistry or flow cytometry

- Disease evaluable by positron-emission tomography scan

- Diagnostic tissue (either frozen or fresh unfixed) available for molecular testing or
willing to undergo a repeat procedure to obtain such tissue

- No CNS involvement by lymphoma

PATIENT CHARACTERISTICS:

Age

- 18 and over

Performance status

- Not specified

Life expectancy

- Not specified

Hematopoietic

- Not specified

Hepatic

- Bilirubin no greater than 3 mg/dL

Renal

- Creatinine no greater than 3 mg/dL

Cardiovascular

- LVEF at least 40%

Other

- Not pregnant or nursing

- Fertile patients must use effective contraception

- No significant organ dysfunction that would preclude study chemotherapy

- HIV negative

PRIOR CONCURRENT THERAPY:

Biologic therapy

- No prior immunotherapy

- No prior biological response modifier therapy

Chemotherapy

- No prior chemotherapy

Endocrine therapy

- Not specified

Radiotherapy

- No prior radiotherapy

- No prior radioimmunotherapy

Surgery

- Not specified