Bendamustine in Combination With Rituximab as a First-line Therapy Followed by Maintenance Therapy With Rituximab in Patients With Follicular Lymphoma

Follicular Lymphoma Clinical Trial

— BRiF  

Official title:

Prospective Multicenter Study: Bendamustine in Combination With Rituximab as a First-line Therapy Followed by Maintenance Therapy With Rituximab in Patients With Follicular Lymphoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02423837
• Other study ID #: FL-RUS-2013
• Status: Recruiting
• Phase: Phase 3
• First received: April 14, 2014
• Last updated: April 19, 2015
• Start date: December 2013
• Est. completion date: April 2021

Study information

• Verified date: April 2015
• Source: National Research Center for Hematology, Russia
• Contact: Elena N Parovichnikova, MD, PhD
• Phone: 495-612-4313
• Email: director[@]blood.ru
• Is FDA regulated: No
• Health authority: Russia: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

• To evaluate the efficacy of bendamustine in combination with rituximab as first line in patients with follicular lymphoma, 1-3A cytological type.

• To evaluate the safety, tolerability and feasibility of bendamustine in combination with rituximab as 1st line in patients with follicular lymphoma, 1-3A cytological type.

• To evaluate the impact of the regimen modification (bendamustine dose modification and/or extension of inter-cycle interval) into duration of complete and partial responses.

• To evaluate estimated treatment duration, reasons of treatment withdrawal.

• To evaluate the possibility of unification and standardization of therapy protocol BR (rituximab 375 mg/m2 on day 1 and bendamustine 90 mg/m2 on days 1-2).

• To evaluate factors affecting overall and progression-free survival.

Description:

Protocol involves 6 courses of rituximab and bendamustine with 26 days interval between each course (one cycle continues 28 days). Control examination will be performed every two courses (28, 56, 84 days of treatment) and will include (physical examination, monitoring of clinical blood tests, biochemical blood tests, computed tomography, ultrasonography, in patients with gastrointestinal tract involvement - fibrogastroduodenoscopy and colonoscopy). Efficacy of therapeutic impact will be estimated as rates of complete remission, partial remission, stable disease or progression based on tumor size reduction comparing with pretreatment data and evaluated using computed tomography and expressed as a percentage. Patients with partial or complete remission or stable disease after 2 courses continue treatment. Patients with tumor progression excluded from issue. Patients which achieved a complete remission after 2 courses may end treatment after 4 courses.

Safety, tolerability and feasibility which implies hematologic and non-hematologic toxicity will be estimated using data of physical examination, monitoring of clinical blood tests, biochemical blood tests and bone marrow analyses (cytological, morphological and genetic tests).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: April 2021
• Est. primary completion date: February 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

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 Ethic Committee

• Men and women patients, 18-75 years old

• ECOG performance status = 3

• No previous treatment with chemotherapy and/or radiation therapy of follicular lymphoma

Exclusion Criteria:

• The patient is participating in any clinical trials and/or receiving the experimental treatment.

• Transformation of follicular lymphoma to large cell lymphoma (for example, follicular lymphoma 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 inclusion into 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 6 months, such as acute myocardial infarction, unstable angina, significant ventricular arrhythmia, severe heart failure (NYNA class IV), stroke, or uncontrolled hypertension.

• Renal impairment (serum creatinine > 150 umol/L), except lymphoid infiltration of kidneys and tumor lysis syndrome.

• Liver failure (except leukemic/lymphoid organ infiltration), acute hepatitis (serum bilirubin > 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 antibacterial therapy) 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 caused by neoplastic process.

• Severe mental disorders (schizophrenia, major depressive syndrome and other productive symptoms).

• 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, hemorrhagic syndrome, hypertension patient may be included into the study

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Follicular Lymphoma
• Lymphoma
• Lymphoma, Follicular

Intervention

Drug:
• Rituximab, bendamustine

Locations

Country	Name	City	State
Russian Federation	National Research Center for Hematology	Moscow

Sponsors (1)

Lead Sponsor	Collaborator
National Research Center for Hematology, Russia

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Efficacy (tumor size evaluation)	tumor size will be estimated using computed tomography, ultrasonography, fibragastroduodenoscopy and colonoscopy	From date of randomization until ending of first line R-B therapy (up to 6 months)	Yes
Primary	hematologic and nonhematologic toxicity (changes in leukocytes and trombocytes count, hemoglobin concentration, biochemical blood tests, electrocardiography)	clinical blood tests, biochemical blood tests, electrocardiography	From date of randomization until ending of first line R-B therapy (up to 6 months)	Yes
Secondary	complete or partial response rates	According to NCCN recomendations	From date of randomization up to 90 months	Yes
Secondary	hematologic and nonhematologic toxicity (clinical blood tests, biochemical blood tests, blood pressure measurement, pulse rate, electrocardiography)	clinical blood tests, biochemical blood tests, blood pressure measurement, pulse rate, electrocardiography	From date of randomization up to 90 months	Yes
Secondary	Dose reduction rate or interval elongation		From date of randomization up to 90 months	Yes
Secondary	Number of patients which underwent full protocol		From date of randomization up to 90 months	Yes
Secondary	lifespan without progression		From date of randomization up to 90 months	Yes