Copanlisib With Ibrutinib for Patients With Recurrent/ Refractory Primary Central Nervous System Lymphoma (PCNSL)

Inclusion Criteria:

- Men and woman who are at least 18 years of age on the day of consenting to the study.

- Histologically documented PCNSL

- Relapsed/refractory PCNSL patients. All recurrent/refractory patients need to have
received at least one prior CNS directed therapy. There is no restriction on the
number of recurrences.

- For recurrent/refractory patients, parenchymal lesions must have unequivocal evidence
of disease progression on imaging (MRI of the brain or head CT) 21 days of study
registration. For patients with leptomeningeal disease only, CSF cytology must
document lymphoma cells and/or imaging findings consistent with CSF disease 21 days of
study registration (at the discretion of the investigator).

- ECOG performance status ≤ 2.

- Life expectancy of > 3 months (in the opinion of the investigator).

- Adequate bone marrow and organ function shown by:

- Absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L

- Platelets ≥ 75 x 10^9/L and no platelet transfusion within the past 14 days prior
to study registration

- Hemoglobin (Hgb) ≥ 8 g/dL and no red blood cell (RBC) transfusion within the past
14 days prior to study registration

- International Normalized Ratio (INR) ≤ 1.5 and PTT (aPTT) ≤ 1.5 times the upper
limit of normal

- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 times the
upper limit of normal

- Serum bilirubin ≤ 1.5 times the upper limit of normal; or total bilirubin ≤ 3
times the upper limit of normal with direct bilirubin within the normal range in
patients with well documented Gilbert Syndrome

- Serum creatinine ≤ 2 times the upper limit of normal

- Lipase ≤ 1.5 x upper limit of normal

- Women of childbearing potential (WOCBP) and men must agree to use effective
contraception when sexually active. This applies for the time period between signing
of the informed consent form and 30 days (for WOCBP) and 90 days (for men) after the
last administration of study treatment. A woman is considered of childbearing
potential, i.e. fertile, following menarche and until becoming post-menopausal unless
permanently sterile. Permanent sterilization methods include but are not limited to
hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal
state is defined as no menses for continuous 12 months without an alternative medical
cause. A high follicle stimulating hormone (FSH) level in the postmenopausal range may
be used to confirm a post-menopausal state in women not using hormonal contraception
or hormonal replacement therapy.

- The investigator or a designated associate is requested to advise the patient how
to achieve highly effective birth control (failure rate of less than 1%), e.g.
intrauterine device (IUD), intrauterine hormone-releasing system (IUS), bilateral
tubal occlusion, vasectomized partner and sexual abstinence

- The use of condoms by male patients is required unless the female partner is
permanently sterile. Female subjects of childbearing potential must have a
negative plasma pregnancy test upon study entry

- Must be able to tolerate MRI/CT scans

- Must be able to tolerate lumbar puncture and/or Ommaya taps

- Must have recovered to grade 1 toxicity from prior therapy

- Able to submit up to 20 unstained formalin-fixed, paraffin-embedded (FFPE) slides from
the initial or most recent tissue diagnosis for correlative studies NOTE: Prior
autologous stem cell transplant as well as prior radiation to the CNS does NOT prevent
patients from enrollment into the trial.

Exclusion Criteria:

Patients eligible for this study must NOT MEET ANY of the following criteria:

- Active concurrent malignancy requiring active therapy

Excluded medical conditions:

- Clinically significant cardiovascular disease such as uncontrolled or symptomatic
arrhythmias, congestive heart failure (New York Heart Association > Class 2), unstable
angina, or myocardial infarction within 6 months of screening, or any Class 3 or 4
cardiac disease as defined by the New York Heart Association Functional Classification

- Uncontrolled hypertension despite optimal medical management (per investigator‟s
assessment)

- Patient has poorly controlled diabetes mellitus with a glycosylated hemoglobin >8% or
poorly controlled steroid-induced diabetes mellitus with a glycosylated hemoglobin of
>8%

- Patient is known to have an uncontrolled active systemic infection (>CTCAE grade 2)
and recent infection requiring intravenous anti-infective treatment that was completed
≤14 days before the first dose of study drug

- Arterial or venous thrombotic or embolic events such as cerebrovascular accident, deep
vein thrombosis or pulmonary embolism within 3 months before the start of study
treatment

- Non-healing wound, ulcer or bone fracture

- Not recovered to a grade 1 from the toxic effects of prior therapy if clinically
relevant in the opinion of the investigator (e.g. alopecia)

- Known bleeding diathesis (eg, von Willebrand‟s disease) or hemophilia

- Known history of infection with human immunodeficiency virus (HIV) or history of
active or chronic infection with hepatitis C virus (HCV) or hepatitis B virus (HBV) as
determined by serologic tests, or any uncontrolled active systemic infection

- Patient underwent major systemic surgery ≤ 2 weeks prior to starting the trial
treatment or who has not recovered from the side effects of such surgery, or who plan
to have surgery within 2 weeks of the first dose of the study drug

- Unable to swallow capsules or disease significantly affecting gastrointestinal
function, such as malabsorption syndrome, resection of the stomach or small bowel, or
complete bowel obstruction

- Any life-threatening illness, medical condition including uncontrolled diabetes
mellitus (DM), uncontrolled hypertension or organ system dysfunction that, in the
opinion of the investigator, could compromise the subject‟s safety or put the study
outcomes at undue risk

- Lactating or pregnant

Excluded previous Therapies and medications:

- Any chemotherapy, external beam radiation therapy, or anticancer antibodies within 21
days of the first dose of study drug

- Prior treatment with a PI3K inhibitor, AKT inhibitor, or mTOR inhibitor (prior
ibrutinib exposure is allowed)

- Any targeted anticancer therapy ≤ 4 weeks or 5 half-lives, whichever is shorter

- Use of radio- or toxin-immunoconjugates within 70 days of the first dose of study drug

- Concurrent use of warfarin or other vitamin K antagonists (need to be stopped 7 days
prior to starting on trial drug)

- Concurrent use of a strong cytochrome P450 (CYP) 3A4/5 inhibitor and inducers (see
Appendix 1) (need to be stopped 2 weeks prior to starting on trial drug)

- Enzyme-inducing antiepileptic drugs (EIAED) need to be discontinued and switched to a
nonnon-EIAED 2 weeks prior to starting on trial drug)

- Patient requires more than 4 mg of dexamethasone daily or the equivalent

- Patient is using systemic immunosuppressant therapy, including cyclosporine A,
tacrolimus, sirolimus, and other such medications, or chronic administration of > 5
mg/day or prednisone or the equivalent. Participants must be off of immunosuppressant
therapy for at least 28 days prior to the first dose of the study drug

- Concurrent systemic immunosuppressant therapy (eg, cyclosporine A, tacrolimus, etc.,
or chronic administration of > 5 mg/day of prednisone) within 28 days of the first
dose of study drug

- Prior allogeneic stem cell transplant