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A Dose Study of Doxil in a Dose Dense, 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell Non-Hodgkin Lymphoma (NHL)> 60 Years or With Compromised Cardiac Status.

Primary Purpose

Diffuse Large B Cell Lymphoma, Lymphoma, Non-Hodgkin

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Doxil
Cyclophosphamide
Vincristine
Prednisone
Rituximab
Pegfilgrastim
Sponsored by
The Alvin and Lois Lapidus Cancer Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diffuse Large B Cell Lymphoma focused on measuring Diffuse Large B Cell Lymphoma, CDOP, Dose Dense, Anne Arbor Stage I-IV, Any IPI score

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 60 years old and older or 18 years old and older with significant/potential cardiac morbidity Diagnosis of diffuse large B cell lymphoma, Ann Arbor stage I-IV, any International Prognostic Index (IPI) score. Previously untreated New York Heart Association (NYHA) classification of Class III or better Baseline ejection fraction (EF) > 25% Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3 Unless attributable to NHL: absolute neutrophil count (ANC) > 1500/uL, platelets > 100,000/uL; hemoglobin > 9.0 g/dl Bilirubin < 1.5 mg/dL (unless related to lymphoma) Hepatic: transaminases < 2.5 x upper limit of normal (ULN) (unless related to lymphoma) Creatinine < 2.5 mg/dl (unless related to lymphoma) Exclusion Criteria: No HIV+ individuals No primary central nervous system (CNS) lymphoma No pregnant or lactating women No serious active infection History of prior malignancy within the last 5 years other than subject's original cancer diagnosis listed in inclusion criteria with the exception of curatively treated basal cell carcinoma.

Sites / Locations

  • Sinai Hospital of BaltimoreRecruiting
  • Northwest Hospital CenterRecruiting

Outcomes

Primary Outcome Measures

Safety assessment: National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTACAE) v3.0
Efficacy: tumor evaluations every three (q 3) cycles

Secondary Outcome Measures

Full Information

First Posted
May 31, 2006
Last Updated
September 25, 2006
Sponsor
The Alvin and Lois Lapidus Cancer Institute
Collaborators
Ortho Biotech Products, L.P.
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1. Study Identification

Unique Protocol Identification Number
NCT00333008
Brief Title
A Dose Study of Doxil in a Dose Dense, 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell Non-Hodgkin Lymphoma (NHL)> 60 Years or With Compromised Cardiac Status.
Official Title
Phase II Dose Study of Doxil in a Dose Dense, 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell NHL > 60 Years or With Compromised Cardiac Status
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Unknown status
Study Start Date
May 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
The Alvin and Lois Lapidus Cancer Institute
Collaborators
Ortho Biotech Products, L.P.

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate the feasibility and tolerability of delivering a full dose, on time schedule of dose-dense CDOP-R (cyclophosphamide, doxil, vincristine, prednisone, and rituximab) in NHL.
Detailed Description
Diffuse large B-cell lymphoma (DLBCL) is the most frequent type of non-Hodgkin's lymphoma with more than half of the patients being over the age of 60 years. Elderly patients with cancer are defined by the American Society of Clinical Oncology as a "special population" due to their disease characteristics, additional health problems, and need for aggressive supportive care strategies to reduce morbidity and mortality. The combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) remains as standard therapy for the treatment of DLBCL, but elderly patients tend to tolerate the CHOP therapy less when compared to younger patients. Cardiac toxicity, as well as decrease in blood counts, are the most common side effects in the elderly population. For these reasons, many doctors are reluctant to use standard combinations and doses of chemotherapy in the elderly for fear of increased morbidity. DLBCL in the elderly is also somewhat unique in that the elderly patients appear to have more aggressive disease and poor overall outcome. In order to maximize the tolerability of treatment and thus potentially enhance overall treatment success in this population, it is necessary to look at alternative treatments. This clinical trial is based on currently accepted standard NHL therapy (CHOP-Rituximab) in which Doxil is substituted for Adriamycin. Growth factor will be used for support of acceptable blood counts. Chemotherapy regimens that include rituximab are now the gold standard for treatment of DLBCL. If indeed, delivering full dose chemotherapy without treatment delays leads to higher remission and cure rates, then this offers a significant proportion of NHL patients who are elderly a chance for cure rather than providing treatment for comfort measures while preserving quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diffuse Large B Cell Lymphoma, Lymphoma, Non-Hodgkin
Keywords
Diffuse Large B Cell Lymphoma, CDOP, Dose Dense, Anne Arbor Stage I-IV, Any IPI score

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
27 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Doxil
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Intervention Type
Drug
Intervention Name(s)
Vincristine
Intervention Type
Drug
Intervention Name(s)
Prednisone
Intervention Type
Drug
Intervention Name(s)
Rituximab
Intervention Type
Drug
Intervention Name(s)
Pegfilgrastim
Primary Outcome Measure Information:
Title
Safety assessment: National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTACAE) v3.0
Title
Efficacy: tumor evaluations every three (q 3) cycles

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 60 years old and older or 18 years old and older with significant/potential cardiac morbidity Diagnosis of diffuse large B cell lymphoma, Ann Arbor stage I-IV, any International Prognostic Index (IPI) score. Previously untreated New York Heart Association (NYHA) classification of Class III or better Baseline ejection fraction (EF) > 25% Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3 Unless attributable to NHL: absolute neutrophil count (ANC) > 1500/uL, platelets > 100,000/uL; hemoglobin > 9.0 g/dl Bilirubin < 1.5 mg/dL (unless related to lymphoma) Hepatic: transaminases < 2.5 x upper limit of normal (ULN) (unless related to lymphoma) Creatinine < 2.5 mg/dl (unless related to lymphoma) Exclusion Criteria: No HIV+ individuals No primary central nervous system (CNS) lymphoma No pregnant or lactating women No serious active infection History of prior malignancy within the last 5 years other than subject's original cancer diagnosis listed in inclusion criteria with the exception of curatively treated basal cell carcinoma.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pam Nickoles, RN, BSN
Phone
410-601-0729
Email
pnickole@lifebridgehealth.org
First Name & Middle Initial & Last Name or Official Title & Degree
Judy Bosley, RN, BSN
Phone
410-601-4392
Email
jbosley@lifebridgehealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen Noga, MD, PhD
Organizational Affiliation
Sinai Hospital of Baltimore, The Alvin and Lois Lapidus Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sinai Hospital of Baltimore
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pam Nickoles, RN, BSN
Phone
410-601-0729
Email
pnickole@lifebridgehealth.org
First Name & Middle Initial & Last Name & Degree
Judy Bosley, RN, BSN
Phone
410-601-4392
Email
jbosley@lifebridgehealth.org
First Name & Middle Initial & Last Name & Degree
Stephen Noga, MD, PhD
Facility Name
Northwest Hospital Center
City
Randallstown
State/Province
Maryland
ZIP/Postal Code
21133
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pam Nickoles, RN, BSN
Phone
410-601-0729
Email
pnickole@lifebridgehealth.org
First Name & Middle Initial & Last Name & Degree
Judy Bosley, RN, BSN
Phone
410-601-4392
Email
jbosley@lifebridgehealth.org
First Name & Middle Initial & Last Name & Degree
Stephen Noga, MD, PhD

12. IPD Sharing Statement

Links:
URL
http://lifebridgehealth.org
Description
The Alvin and Lois Lapidus Cancer Institute; Protocols

Learn more about this trial

A Dose Study of Doxil in a Dose Dense, 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell Non-Hodgkin Lymphoma (NHL)> 60 Years or With Compromised Cardiac Status.

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