A Study Evaluating the Safety and Efficacy of Atezolizumab in Combination With Obinutuzumab Plus Lenalidomide in Patients With Relapsed or Refractory Follicular Lymphoma

Roche

Status and phase

Completed

Phase 2

Phase 1

Conditions

Lymphoma, Follicular

Treatments

Drug: Atezolizumab (MPDL3280A) [TECENTRIQ]

Drug: Lenalidomide

Drug: Obinutuzumab

Study type

Interventional

Funder types

Industry

Identifiers

NCT02631577

BO29562

2015-002467-42 (EudraCT Number)

Details and patient eligibility

About

This study will evaluate the safety, efficacy, pharmacokinetics and immunogenicity of induction treatment consisting of atezolizumab in combination with obinutuzumab plus lenalidomide in patients with relapsed or refractory follicular lymphoma (FL), followed by maintenance treatment with atezolizumab plus obinutzumab plus lenalidomide in patients who achieve a complete response (CR), a partial response (PR), or stable disease at end of induction.

Enrollment

38 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2
Relapsed or refractory FL after treatment with at least one prior chemoimmunotherapy regimen that included an anti-CD20 monoclonal antibody and for which no other more appropriate treatment option exists as determined by the investigator
Histologically documented CD20-positive lymphoma as determined by the local laboratory
Fluorodeoxyglucose-avid lymphoma (i.e., PET-positive lymphoma)
At least one bi-dimensionally measurable lesion (>1.5 cm in its largest dimension by CT scan or magnetic resonance imaging [MRI])
Availability of a representative tumor specimen and the corresponding pathology report for retrospective central confirmation of the diagnosis of FL
Agreement to comply with all local requirements of the lenalidomide risk minimization plan
For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use two adequate methods of contraception, including at least one method with a failure rate of <1% per year, for at least 28 days prior to Day 1 of Cycle 1, during the treatment period (including periods of treatment interruption), and for at least 18 months after the last dose of study treatment
For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures and agreement to refrain from donating sperm for at least 3 months after the last dose of study treatment

Exclusion criteria

Grade 3b follicular lymphoma
History of transformation of indolent disease to diffuse large B-cell lymphoma (DLBCL)
Known CD20-negative status at relapse or progression
Central nervous system lymphoma or leptomeningeal infiltration
Prior allogeneic stem-cell transplantation (SCT)
Completion of autologous SCT within 100 days prior to Day (D) 1 of Cycle (C) 1
Prior standard or investigational anti-cancer therapy as specified in protocol
History of resistance to lenalidomide or response duration of <1 year
Treatment with systemic immunosuppressive medications
History of solid organ transplantation
Clinically significant toxicity from prior therapy that has not resolved to Grade <=2 (according to the National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE], v4.0) prior to Day 1 of Cycle 1
History of erythema multiforme, Grade >= 3 rash, or blistering following prior treatment with immunomodulatory derivatives such as thalidomide and lenalidomide
Active bacterial, viral, fungal, or other infection
Positive for hepatitis B surface antigen (HBsAg), total hepatitis B core antibody (HBcAb), or hepatitis C virus (HCV) antibody at screening
Known history of HIV positive status
History of progressive multifocal leukoencephalopathy
History of autoimmune disease
Contraindication to treatment for TE prophylaxis
Grade <= 2 neuropathy
History of other malignancy that could affect compliance with the protocol or interpretation of results
Evidence of any significant, uncontrolled concomitant disease
Inadequate hematologic function (unless due to underlying lymphoma)
Abnormal laboratory values (unless due to underlying lymphoma)
Pregnant or lactating or intending to become pregnant during the study