Combination Chemotherapy and Rituximab in Treating Patients With Primary Mediastinal Diffuse Large B-Cell Lymphoma

A Clinico-Pathologic Study of Primary Mediastinal B-Cell Lymphoma (IELSG 26)

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Giving rituximab together with one of five different combination chemotherapy regimens may kill more cancer cells.

PURPOSE: This clinical trial is studying giving rituximab together with combination chemotherapy to see how well it works in treating patients with primary mediastinal diffuse large B-cell lymphoma.

Study Overview

• Status: Unknown
• Conditions: Lymphoma
• Intervention / Treatment: Drug: cyclophosphamide; Drug: methotrexate; Drug: doxorubicin hydrochloride; Drug: vincristine sulfate; Drug: prednisone; Biological: bleomycin sulfate; Biological: filgrastim; Drug: prednisolone; Drug: ifosfamide; Drug: etoposide phosphate; Drug: cytarabine; Drug: vindesine; Biological: rituximab

Detailed Description

OBJECTIVES:

Primary

• To systematically analyze the phenotype and molecular characteristics in patients with primary mediastinal diffuse large B-cell lymphoma.
• To determine the PET response rate following chemoimmunotherapy in these patients.

Secondary

• To obtain data, on a nonrandomized basis, regarding the outcomes of treatment using different chemoimmunotherapy regimens and using or omitting mediastinal radiotherapy, depending upon the practice of the participating institutions.
• To analyze progression-free and overall survival in patients treated with these regimens.

OUTLINE: This is a multicenter study.

Patients receive any one of the following standard chemoimmunotherapy regimens.

• Cohort 1 (R-CHOP-21): Patients receive rituximab IV, cyclophosphamide IV, doxorubicin hydrochloride IV, and vincristine IV on day 1 and oral prednisolone on days 1-5. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.
• Cohort 2 (R-CHOP-14): Patients receive rituximab IV, cyclophosphamide IV, doxorubicin hydrochloride IV, and vincristine IV on day 1, oral prednisolone on days 1-5, and filgrastim (G-CSF) subcutaneously (SC) on days 5-12. Treatment repeats every 14 days in the absence of disease progression or unacceptable toxicity.
• Cohort 3 (R-MACOP-B): Patients receive rituximab IV on days 1, 22, 43, 64, 85, and 106; cyclophosphamide IV and doxorubicin hydrochloride IV on days 1, 15, 29, 43, 57, and 71; methotrexate IV on days 8, 36, and 64; vincristine IV on days 8, 22, 36, 50 ,64, and 78; bleomycin IV on days 22, 50, and 78; and oral prednisolone on days 1-84, followed by a taper.
• Cohort 4 (R-VACOP-B): Patients receive rituximab IV on days 1, 22, 43, 64, 85, and 106; cyclophosphamide IV on days 1, 29, and 57; doxorubicin hydrochloride IV on days 1, 15, 29, 43, 57, and 71; etoposide phosphate IV on days 15, 16, 43, 44, 71, and 72; vincristine IV and bleomycin IV on days 8, 22, 36, 50, 64, and 78; and oral prednisolone on days 1-84, followed by a taper.
• Cohort 5 (R-ACVBP): Patients receive rituximab IV, doxorubicin hydrochloride IV, and cyclophosphamide IV on day 1; vindesine IV and bleomycin IV on days 1 and 5; oral prednisone on days 1-5; methotrexate intrathecally on day 2; and G-CSF SC on days 6-13 for 4 courses in the absence of disease progression or unacceptable toxicity. After completion of 4 courses of R-ACVBP, patients receive consolidation therapy comprising high-dose methotrexate IV, rituximab IV, ifosfamide IV, etoposide phosphate IV, and cytarabine SC according to protocol GELA LNH03-2B.

Patients with an International Prognostic Index score of 4 or greater or disease in close proximity to the spinal cord or cerebral meninges may receive prophylactic treatment to the CNS according to local protocol.

Beginning 8 weeks after completion of chemoimmunotherapy, patients undergo radiotherapy to the original tumor volume according to local protocol.

Fresh or fixed tissue from prior biopsy is obtained if possible. Samples are analyzed for CD3, CD20, CD30, CD15, CD10, Bcl-6, Bcl-2, MAL protein (if available), and Ki-67 via immunohistochemistry.

After completion of study treatment, patients are followed periodically.

• Study Type: Interventional
• Enrollment (Anticipated): 120
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United Kingdom
  • London, United Kingdom
    • Recruiting
    • Saint Bartholomew's Hospital
    • Contact: Contact Person; Phone Number: 44-207-796-3979; Email: silvia.montoto@cancer.org.uk
  • England
    • Leeds, England, United Kingdom, LS9 7TF
      • Recruiting
      • Leeds Cancer Centre at St. James's University Hospital
    • London, England, United Kingdom, SW17 0QT
      • Recruiting
      • St. George's Hospital
      • Contact: Contact Person; Phone Number: 44-208-725-2425; Email: rpetteng@sghms.ac.uk
    • Manchester, England, United Kingdom, M20 4BX
      • Recruiting
      • Christie Hospital
      • Contact: Contact Person; Phone Number: 44-845-226-3000
    • Northwood, England, United Kingdom, HA6 2RN
      • Recruiting
      • Mount Vernon Cancer Centre at Mount Vernon Hospital
      • Contact: Contact Person; Phone Number: 44-1923-826-111
    • Sheffield, England, United Kingdom, S1O 2SJ
      • Recruiting
      • Cancer Research Centre at Weston Park Hospital
      • Contact: Contact Person; Phone Number: 44-114-226-5007; Email: b.w.hancock@sheffield.ac.uk
    • Southampton, England, United Kingdom, SO16 6YD
      • Recruiting
      • Southampton General Hospital
      • Contact: Contact Person; Phone Number: 44-238-079-6186; Email: johnsonp@soton.ac.uk
    • Sutton, England, United Kingdom, SM2 5PT
      • Recruiting
      • Royal Marsden - Surrey
      • Contact: Contact Person; Phone Number: 44-208-661-3279; Email: david.cunningham@rmh.nhs.uk

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

DISEASE CHARACTERISTICS:

• Histologically confirmed primary mediastinal diffuse large B-cell lymphoma

  • CD20-positive disease
  • Any stage of disease
  • Must have a dominant mass within the anterior mediastinum

PATIENT CHARACTERISTICS:

• ANC ≥ 1.5 x 10^9/L (unless due to lymphoma)
• Platelets ≥ 100 x 10^9/L (unless due to lymphoma)
• WBC ≥ 3.0 x 10^9/L (unless due to lymphoma)
• Serum creatinine ≤ 2 times upper limit of normal (ULN) (unless due to lymphoma)
• AST/ALT ≤ 2.5 times ULN (unless due to lymphoma)
• Total bilirubin ≤ 2.5 times ULN (unless due to lymphoma)
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• Must be fit to receive chemotherapy with curative intent

• No evidence of clinically significant cardiac disease* within the past 12 months, including any of the following:

  • Symptomatic ventricular arrhythmias
  • Congestive heart failure
  • Myocardial infarction NOTE: * Cardiac compromise due to local extension of lymphoma will not be an exclusion criterion in the absence of other cardiac disease.
• No known HIV infection
• No psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
• Able and willing to give informed consent and to undergo staging, including PET scanning

PRIOR CONCURRENT THERAPY:

• No prior treatment for lymphoma
• Prior corticosteroids for up to 1 week allowed for the relief of local compressive symptoms

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Cohort 1; Patients receive rituximab IV, cyclophosphamide IV, doxorubicin hydrochloride IV, and vincristine IV on day 1. Patients also receive oral prednisolone on days 1-5. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.	Drug: cyclophosphamide; Given IV; Drug: doxorubicin hydrochloride; Given IV; Drug: vincristine sulfate; Given IV; Drug: prednisolone; Given orally; Biological: rituximab; given IV
Experimental: Cohort 2; Patients receive rituximab IV, cyclophosphamide IV, doxorubicin hydrochloride IV, and vincristine IV on day 1, oral prednisolone on days 1-5, and filgrastim (G-CSF) subcutaneously (SC) on days 5-12. Treatment repeats every 14 days in the absence of disease progression or unacceptable toxicity.	Drug: cyclophosphamide; Given IV; Drug: doxorubicin hydrochloride; Given IV; Drug: vincristine sulfate; Given IV; Biological: filgrastim; Given subcutaneously; Drug: prednisolone; Given orally; Biological: rituximab; given IV
Experimental: Cohort 3; Patients receive rituximab IV on days 1, 22, 43, 64, 85, and 106; cyclophosphamide IV and doxorubicin hydrochloride IV on days 1, 15, 29, 43, 57, and 71; methotrexate IV on days 8, 36, and 64; vincristine IV on days 8, 22, 36, 50 ,64, and 78; bleomycin IV on days 22, 50, and 78; and oral prednisolone on days 1-84, followed by a taper.	Drug: cyclophosphamide; Given IV; Drug: methotrexate; Given IV; Drug: doxorubicin hydrochloride; Given IV; Drug: vincristine sulfate; Given IV; Biological: bleomycin sulfate; Given IV; Drug: prednisolone; Given orally; Biological: rituximab; given IV
Experimental: Cohort 4; Patients receive rituximab IV on days 1, 22, 43, 64, 85, and 106; cyclophosphamide IV on days 1, 29, and 57; doxorubicin hydrochloride IV on days 1, 15, 29, 43, 57, and 71; etoposide phosphate IV on days 15, 16, 43, 44, 71, and 72; vincristine IV and bleomycin IV on days 8, 22, 36, 50, 64, and 78; and oral prednisolone on days 1-84, followed by a taper.	Drug: cyclophosphamide; Given IV; Drug: doxorubicin hydrochloride; Given IV; Drug: vincristine sulfate; Given IV; Biological: bleomycin sulfate; Given IV; Drug: prednisolone; Given orally; Drug: etoposide phosphate; Given IV; Biological: rituximab; given IV
Experimental: Cohort 5; Patients receive rituximab IV, doxorubicin hydrochloride IV, and cyclophosphamide IV on day 1; vindesine IV and bleomycin IV on days 1 and 5; oral prednisone on days 1-5; methotrexate intrathecally on day 2; and G-CSF SC on days 6-13 for 4 courses in the absence of disease progression or unacceptable toxicity. After completion of 4 courses of R-ACVBP, patients receive consolidation therapy comprising high-dose methotrexate IV, rituximab IV, ifosfamide IV, etoposide phosphate IV, and cytarabine SC according to protocol GELA LNH03-2B.	Drug: cyclophosphamide; Given IV; Drug: methotrexate; Given IV; Drug: doxorubicin hydrochloride; Given IV; Drug: prednisone; Given orally; Biological: bleomycin sulfate; Given IV; Biological: filgrastim; Given subcutaneously; Drug: ifosfamide; Given IV; Drug: etoposide phosphate; Given IV; Drug: cytarabine; Given subcutaneously; Drug: vindesine; Given IV; Biological: rituximab; given IV

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Complete response rate on PET scanning at the completion of chemoimmunotherapy

Secondary Outcome Measures

Outcome Measure
Progression-free survival
Death
Survival time

Collaborators and Investigators

• Sponsor: University Hospital Southampton NHS Foundation Trust
• Investigators: Principal Investigator: Peter Johnson, MD, University Hospital Southampton NHS Foundation Trust

Study record dates

Study Major Dates

• Study Start: June 1, 2007

Study Registration Dates

• First Submitted: June 3, 2008
• First Submitted That Met QC Criteria: June 3, 2008
• First Posted (Estimate): June 4, 2008

Study Record Updates

• Last Update Posted (Estimate): July 8, 2009
• Last Update Submitted That Met QC Criteria: July 7, 2009
• Last Verified: July 1, 2009

More Information

Terms related to this study

• Keywords: stage III adult diffuse large cell lymphoma; stage IV adult diffuse large cell lymphoma; noncontiguous stage II adult diffuse large cell lymphoma; contiguous stage II adult diffuse large cell lymphoma; stage I adult diffuse large cell lymphoma
• Additional Relevant MeSH Terms: Immune System Diseases; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Lymphoma; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Anti-Infective Agents; Antiviral Agents; Nucleic Acid Synthesis Inhibitors; Enzyme Inhibitors; Anti-Inflammatory Agents; Antirheumatic Agents; Antimetabolites, Antineoplastic; Antimetabolites; Antineoplastic Agents; Immunosuppressive Agents; Immunologic Factors; Tubulin Modulators; Antimitotic Agents; Mitosis Modulators; Glucocorticoids; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Antineoplastic Agents, Hormonal; Antineoplastic Agents, Alkylating; Alkylating Agents; Myeloablative Agonists; Antineoplastic Agents, Phytogenic; Topoisomerase II Inhibitors; Topoisomerase Inhibitors; Antineoplastic Agents, Immunological; Dermatologic Agents; Antibiotics, Antineoplastic; Reproductive Control Agents; Abortifacient Agents, Nonsteroidal; Abortifacient Agents; Folic Acid Antagonists; Prednisolone; Cyclophosphamide; Etoposide; Etoposide phosphate; Ifosfamide; Rituximab; Prednisone; Doxorubicin; Liposomal doxorubicin; Cytarabine; Methotrexate; Vincristine; Bleomycin; Vindesine
• Other Study ID Numbers: CDR0000588011; USCTU-IELSG-26-RHM-CAN0546; EU-20818; EudraCT 2006-005794-22; USCTU-07/Q1704/68