| Eligibility |
Inclusion Criteria:
1. Age >18 years.
2. Histologically confirmed diffuse large B-cell lymphoma (DLBCL) , including transformed
low grade lymphoma, with either:
1. Refractory disease: defined as disease progression while receiving their most
recent prior cytotoxic chemotherapy (single-agent immunotherapy as maintenance is
not considered cytotoxic therapy).
2. Persistent disease: defined as stable disease or partial response at the
completion of their most recent prior cytotoxic chemotherapy.
3. Relapsed/recurrent disease: defined as complete response at the end of their most
recent prior cytotoxic chemotherapy with subsequent relapse or disease
recurrence.
3. Subjects must have received prior rituximab and may have received up to 5 prior
regimens containing cytotoxic chemotherapies.
4. Subjects must not be candidates for high-dose chemotherapy with autologous stem cell
support (ASCT), due to one or more of the following factors: relapse after high dose
chemotherapy, age, comorbid disease, performance status, or persisting toxicities from
prior chemotherapy.
5. Absolute neutrophil count (ANC) >1.0 x 109/L, unless related to bone marrow
infiltration.
6. At least 1 measurable disease lesion that is >1.0 cm in 2 perpendicular dimensions,
with the product diameter >2.25 cm2 by computed tomography (CT) or magnetic resonance
imaging (MRI).
7. Negative serum pregnancy test within 1 week before first treatment if the subject is a
woman of childbearing potential. The use of highly-effective contraception methods*
are required during the study for women of child-bearing potential. Due to the
toxicity of idelalisib, women who will use a hormonal contraceptive must in addition
also use a barrier method, since it is currently unknown whether idelalisib may reduce
the effectiveness of hormonal contraceptives. A woman of childbearing potential is
defined as one who is biologically capable of becoming pregnant.
8. WHO performance status 0 - 3.
9. Written informed consent.
Exclusion Criteria:
1. Prior allogeneic hematopoietic stem cell transplant (HSCT).
2. Prior treatment with PI3K inhibitors.
3. Serum total bilirubin = 1.5 x ULN (unless elevated due to Gilbert's syndrome).
4. Serum ALT and AST ? 2.5 x ULN.
5. Estimated Creatinine Clearance < 10 ml/min.
6. Known seropositivity for human immunodeficiency virus (HIV).
7. Known history of drug induced liver injury, chronic active hepatitis C (HCV), chronic
active hepatitis B (HBV), alcoholic liver disease, non-alcoholic steatohepatitis,
primary biliary cirrhosis, on-going extra-hepatic obstruction caused by
cholelithiasis, cirrhosis of the liver or portal hypertension.
8. Known history of drug induced pneumonitis.
9. On-going inflammatory bowel disease.
10. Evidence of serious active infection (eg, requiring an intravenous [IV] antibiotic,
antiviral, or antifungal agent), or subjects with a recent history of deep tissue
infections such as fascitis or osteomyelitis.
11. Chemotherapy, cancer immunosuppressive therapy, growth factors (except
erythropoietin), or investigational drugs/devices <10 days before first dose of
investigational product in this study. Subjects receiving high doses of
corticosteroids must have been tapered to a stable dose at least 7 days before the
first dose of investigational product.
12. Pregnant or breastfeeding women.
13. Symptomatic central nervous system (CNS) NHL; a lumbar puncture is not required unless
CNS involvement with NHL is clinically suspected.
14. Unstable or severe uncontrolled medical condition (eg, unstable cardiac function,
unstable pulmonary condition).
15. Concurrent active malignancy other than nonmelanoma skin cancer or carcinoma in situ
of the cervix. Subjects with previous malignancies are eligible provided that they
have been disease free for >2 years.
16. Previous myocardial infarction or pulmonary hypertension <6 months before first dose
of investigational product.
17. History of clinically significant ventricular arrhythmia, prolonged QTc interval or
unexplained syncope.
18. Psychiatric illness or condition which could interfere with their ability to
understand the requirements of the study.
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