Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Sunnybrook Health Sciences Centre
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients with 1-2 relapses of WHO Classification follicle centre NHL grade 1-2/3. Patients must have achieved at least a PR to previous treatment.
Central pathology review before registration
Ann Arbor stage III or IV
Measurable disease: defined as clinically or radiologically documented disease with at least one site bidimensionally measurable using clinical exam, CT or MRI performed in the 3 weeks prior to study enrollment.
ECOG performance status of \<2.
Patients may have received not more than 1 prior course (4 infusions) of rituximab. Timing of rituximab must exceed 12 months prior to registration. Patients must have demonstrated at least a PR to rituximab if previously administered.
Patient consent according to institutional and university human experimentation committee requirements
Adequate Renal, hepatic and hematopoietic function test unless the abnormal values are thought to be due to involvement with lymphoma as defined by:
Hb\> 85 ANC \>1000/mm3 Platelets \>100,000/mm3 Serum/Total Bilirubin \>=2 SI units AST/ALT \<2x Upper Limit of Normal
You may not be if
Positive serology for HIV
Uncontrolled Infection
Pregnancy
CNS Metastases
History of Psychiatric Disorder
Other Malignancy (except nonmelanoma skin cancer)
Serious non-malignant disease (e.g., congestive heart failure, or active uncontrolled bacterial, viral, or fungal infections), or other conditions, which, in the opinion of the investigator and/or the sponsor, would compromise other protocol objectives.
Major surgery, other than diagnostic surgery, within four weeks.
Presence of anti-murine antibody (HAMA) reactivity. These laboratory results must be available prior to receiving treatment for those patients
who have received prior murine proteins or patients who have allergies to murine proteins.
New York Heart Association Class III or IV heart disease (see Appendix H, Clinical Evaluation of Functional Capacity of Patients with Heart Disease in Relation to Ordinary Physical Activity) or myocardial infarction within the past six months.
Treatment with an investigational drug within 30 days or five half-lives (of the study drug with the longest half-life) prior to entry into the study, which ever is longer.
Previous chemotherapy, immunotherapy, radiotherapy, or investigational therapy for the treatment of other malignancy except basal cell or squamous cell skin cancer or carcinoma in situ of the cervix within the last 5 years.
History of allergic reactions to compounds chemically related to Rituximab.
Refusal to practice contraception if of reproductive potential.
Clareo Health | Treatment of Follicular Lymphoma With High Dose Therapy and Stem Cell Support Followed by Rituximab and Alpha Interferon
