Phase
Condition
Lymphoma
Follicular Lymphoma
Lymphoproliferative Disorders
Treatment
N/AClinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients with the diagnosis of follicular lymphoma confirmed by immunohistochemistry (IHC) analysis in the reference laboratory
Written informed consent for the use of personal data approved by Independent EthicCommittee
Men and women patients, 18-75 years old
ECOG performance status ≤ 3
No previous treatment with chemotherapy and/or radiation therapy of follicularlymphoma
Exclusion
Exclusion Criteria:
The patient is participating in any clinical trials and/or receiving the experimentaltreatment.
Transformation of follicular lymphoma to large cell lymphoma (for example, follicularlymphoma IIIB graduation, diffuse large B-cell lymphoma).
Central nervous system involvement.
The presence of a second malignancy within the last 5 years prior to the inclusioninto the study except for adequately treated basal cell or squamous cell skin cancer,in situ cervical cancer or prostate cancer.
Clinically significant cardiovascular or cerebro-vascular disease in the past 6months, such as acute myocardial infarction, unstable angina, significant ventriculararrhythmia, severe heart failure (NYNA class IV), stroke, or uncontrolledhypertension.
Renal impairment (serum creatinine > 150 umol/L), except lymphoid infiltration ofkidneys and tumor lysis syndrome.
Liver failure (except leukemic/lymphoid organ infiltration), acute hepatitis (serumbilirubin > 2 x ULN, the activity of ALT and AST > 4 x ULN, prothrombin index < than 50%).
Uncontrolled diabetes mellitus (serum glucose > 15 mmol/L)
Sepsis (septicopyemic focuses, hemodynamic instability, inefficiency of antibacterialtherapy) or acute infectious diseases.
HIV, hepatitis B and C (including the absence of the Hbc and Hbs antibodies).
Life-threatening bleeding, except of bleeding from the gastrointestinal tract causedby neoplastic process.
Severe mental disorders (schizophrenia, major depressive syndrome and other productivesymptoms).
Physical failure requiring constant care, cachexia (total protein < 35 g/L).
Known hypersensitivity to rituximab components.
Known hypersensitivity to bendamustine components.
Pregnant or currently breast-feeding woman
Neutrophils count < 1500/mm3 and/or platelets count < 75000/mm3.
Surgery prior 15 days before therapy initiation.
In case of serious infectious complications relief, uncontrolled diabetes, hemorrhagicsyndrome, hypertension patient may be included into the study
Study Design
Study Description
Connect with a study center
National Research Center for Hematology
Moscow, 125167
Russian FederationActive - Recruiting

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.