Obinutuzumab in Combination With GDP Chemotherapy in Patients With Relapsed or Refractory Non-Hodgkin Lymphoma

Sponsor

University Health Network, Toronto (Other)

Overall Status

Completed

CT.gov ID

NCT02750670

Collaborator

Hoffmann-La Roche (Industry), Ozmosis Research Inc. (Industry)

Enrollment

Location

Arm

46.9

Actual Duration (Months)

0.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a pilot study to determine the overall survival rate and toxicities of obinutuzumab given with GDP chemotherapy for relapsed or refractory CD20+ aggressive non-Hodgkin lymphoma. Patients who have CD20+ and progressed R-CHOP therapy will be enrolled into the study. About 30 patients are planned to be enrolled from Princess Margaret Cancer Centre.

If the enrollment is very slow then additional site may be included. Patients will receive Obinutuzumab +GDP for 3 cycles intravenously. CT scan will be used to evaluate the response rate after cycle 2 and PET-CT will be used after cycle 3. Responders (complete metabolic response, partial metabolic response) should proceed to autologous stem cell transplant (ASCT). Patients who have progressed after three cycles or less are to have their protocol treatment discontinued, with subsequent treatment at investigator discretion. Patients will be followed up to 24 months from transplant done or last chemo. Mandatory tissue submission and optional tissue and blood submission are required for the correlative component of this study.

Condition or Disease	Intervention/Treatment	Phase
Lymphoma, Non-Hodgkin's	Drug: Obinutuzumab Drug: Gemcitabine Drug: Dexamethasone Drug: Cisplatin	Phase 2

Study Design

Study Type:

Interventional

Actual Enrollment :

30 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Pilot Study of Obinutuzumab in Combination With GDP Chemotherapy for the Treatment of Relapsed or Refractory CD20+ Aggressive Non-Hodgkin Lymphoma

Actual Study Start Date :

Mar 15, 2017

Actual Primary Completion Date :

Sep 9, 2020

Actual Study Completion Date :

Feb 9, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: GD2P Obinutuzumab 1000mg by IV for 1.5-6.5 hours with Gemcitabine 1000mg/m^2 by IV for 30 minutes with dexamethasone 40mg by mouth daily and Cisplatin 75mg/m^2 by IV for 1 hour all for a duration of 3 cycles	Drug: Obinutuzumab Type II anti-CD20 monoclonal antibody Other Names: GAZYVA Drug: Gemcitabine Antineoplastic agent Drug: Dexamethasone Corticosteroid Other Names: Decadron Drug: Cisplatin Antineoplastic Agent

Arm

Intervention/Treatment

Experimental: GD2P

Obinutuzumab 1000mg by IV for 1.5-6.5 hours with Gemcitabine 1000mg/m^2 by IV for 30 minutes with dexamethasone 40mg by mouth daily and Cisplatin 75mg/m^2 by IV for 1 hour all for a duration of 3 cycles

Drug: Obinutuzumab

Type II anti-CD20 monoclonal antibody

Other Names:

GAZYVA

Drug: Gemcitabine

Antineoplastic agent

Drug: Dexamethasone

Corticosteroid

Other Names:

Decadron

Drug: Cisplatin

Antineoplastic Agent

Outcome Measures

Primary Outcome Measures

The overall response rate (ORR) of G2DP by investigator assessment based on conventional CT imaging. [42 days]

Secondary Outcome Measures

The ORR rate by central review of conventional CT imaging after 2 cycles of G2DP [42 days]
The Complete Response (CR) rate by FDG-PET scan [Post 63 days]
The rate of successfully proceeding to autologous stem cell transplant (ASCT) [Post 63 days]
Progression Free Survival (PFS) post ASCT (in transplanted patients) or after protocol discontinuation (in patients not transplanted). [Up to 2 years]
The percentage of patients requiring dose reduction for hematologic toxicity. [Up to 63 days]
Correlative studies on patient specimens markers of disease response (in tumor and blood/plasma) as well as to identify blood/plasma markers that provide additional discriminative information to FDG-PET scans [Up to 2 years]
The Complete Response (CR) rate by central review of conventional CT imaging after 2 cycles of G2DP [42 days]
Overall Survival (OS) post ASCT (in transplanted patients) or after protocol discontinuation (in patients not transplanted). [Up to 2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:

16 Years to 70 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Patients with histologic diagnosis for one of the following histologies according to the World Health Organization: documented at initial diagnosis or at relapse:

Diffuse large cell lymphoma, B-cell (includes primary mediastinal B-cell lymphoma, T-cell rich B-cell lymphoma);
Previous indolent lymphoma (follicular lymphoma, marginal zone lymphoma, including extranodal MALT lymphoma, lymphoplasmacytoid lymphoma) with transformation to diffuse large B-cell lymphoma at relapse (biopsy proof of transformation is mandatory);
Follicular lymphoma grade 3B;
Biopsy proof of disease at initial diagnosis is mandatory. A biopsy at relapse is mandatory. A histological diagnosis (core or excisional biopsy) is strongly encouraged; a cytological diagnosis is acceptable only in the event that tissue cannot be obtained.

Patients must be CD20+ in order to be eligible for the study.

Clinically and/or radiologically measurable disease (1 site bidimensionally measurable). Measurements/ evaluations must be done within 28 days prior to registration.

Baseline FDG-PET scan, if available, must be positive (known FDG-avid lymphoma)

Patient must have had at least one previous regimen of therapy for their disease. Patients must have relapsed or progressed after R-CHOP chemotherapy or equivalent.
Patient age is ≥16 years. Patients older than 70 years of age are not recommended for this study. (Note that the lower age limit at each centre will be determined by that centre's policy regarding the age at which an individual may sign his or her own consent.)
ECOG performance status of 0, 1, 2 or 3.
Patient must be considered fit for intensive chemotherapy and ASCT and an appropriate candidate to receive salvage chemotherapy and ASCT.
Laboratory Requirements: (must be done within 14 days of registration)

Hematology:

Granulocytes (AGC) > 1.0 x 109/L (independent of growth factor support)
Platelets > 100 x 109/L (50 x 109/L if bone marrow involvement by lymphoma, independent of transfusion support)

Biochemistry:

AST and ALT < 3x ULN
Serum total bilirubin < 1.5x ULN (≤ 5x ULN if Gilberts Disease)
Serum Creatinine < 1.5x ULN (or estimated GFR of ≥40 mL/min/1.73m2 using Cockcroft Gault formula)
International normalized ratio (INR) > 1.5 × the ULN in the absence of therapeutic anticoagulation
Partial thromboplastin time (PTT) or activated partial thromboplastin time (aPTT)
1.5 × the ULN in the absence of a lupus anticoagulant

A Women of childbearing potential (WOCBP) is defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy or bilateral oophorectomy) and is not postmenopausal. Menopause is defined as 12 months of amenorrhea in a woman over age 45 years in the absence of other biological or physiological causes. Women of child bearing potential (who are heterosexually active) and men (who are sexually active with WOCBP), must be practicing a highly effective method of birth control (Pearl Index <1) such as oral contraceptives, intrauterine device, sexual abstinence or barrier method of contraception in conjunction with spermicidal jelly during study treatment and in female patients for 18 months after end of antibody treatment Men must agree to not donate sperm during and after the study. These restrictions apply for 18 months after the last dose of study drug.

Women of childbearing potential must have a pregnancy test taken (either by serum beta-human chorionic gonadotropin [β-hCG]) or urine) and proven negative within 14 days prior to registration.

Women who are pregnant or breastfeeding are ineligible for this study.

Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to enrollment in the trial to document their willingness to participate.
Patients must be accessible for treatment and follow-up. Patients randomized on this trial must be treated and followed at the participating centre. Investigators must assure themselves the patients randomized on this trial will be available for complete documentation of the treatment, response assessment, adverse events, and follow-up.
Protocol treatment is to begin within 5 working days of patient registration

Exclusion Criteria:

Patients who have been previously treated with obinutuzumab.
Life expectancy < 90 days
Patients with a history of other malignancies, except: adequately treated non-melanoma skin cancer and superficial bladder cancer, curatively treated in-situ cancer of the cervix or breast, or localized excised prostate cancer, other solid tumors curatively treated with no evidence of disease for > 5 years.
Active and uncontrolled central nervous system involvement, meningeal or parenchymal. Patients with CNS disease at initial presentation and who are in a CNS CR at the time of relapse are eligible. MRI scanning and / or lumbar puncture should be performed if there is clinical suspicion of active CNS disease.
Patients with symptoms suggestive of Progressive Multifocal Leukoencephalopathy (PML).
Major surgery performed within 4 weeks prior to registration.
Known history of human immunodeficiency virus (HIV), active Hepatitis C Virus infection, active Hepatitis B Virus infection or any uncontrolled active systemic infection requiring intravenous (IV) antibiotics. Patients with positive hepatitis B serology are defined as positive Hepatitis B surface antigen (HBsAg) or core antibody (anti-HBc). These patients should consult liver disease experts before start of treatment and should be monitored and managed following local medical standards to prevent hepatitis reactivation. Patients with Hepatitis B serology suggestive of infection are eligible if they are HBV DNA negative and concurrently treated with anti-viral therapy. Patients with a past history of hepatitis C who have eradicated the virus (defined as negative PCR for HCV RNA) are eligible.
Patients who have been vaccinated with live, attenuated vaccines within 4 weeks prior to registration.
Known history of stroke or intracranial hemorrhage within 6 months prior to registration.
Clinically significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure, or myocardial infarction within 6 months of Screening, or any Class 3 (moderate) or Class 4 (severe) cardiac disease as defined by the New York Heart Association Functional Classification.
Any serious active disease or co-morbid medical condition, including psychiatric illness, judged by the local investigator to preclude safe administration of the planned protocol treatment or required follow-up.
Any other serious intercurrent illness, life threatening condition, organ system dysfunction, or medical condition judged by the local investigator to compromise the subject's safety, preclude safe administration of the planned protocol treatment or required follow-up, including (for example):

Active, uncontrolled bacterial, fungal, or viral infection, history of chronic or recurrent infection
Clinically significant cardiac dysfunction or cardiovascular disease.

Patients are not eligible if they have a known hypersensitivity to the study drugs or their component, or a history of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies, or a known sensitivity or allergy to murine products