| Eligibility |
Inclusion Criteria:
Patients must meet the following criteria for study entry:
1. Signed Informed Consent Form
2. Age 18 years at the time of signing Informed Consent Form
3. Ability to comply with the study protocol
4. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2
5. Histologically confirmed relpased and/or refractory B-ALL with =5% marrow blasts or
marrow MRD+ (=0.1%) disease. At least 50% of the blasts must express CD20. Relapsed
disease is defined as disease relapse after achieving an initial response to prior
therapies. For patients in 1st relapse of their disease, those with CR1 duration >12
months are excluded. Refractory disease is defined as disease refractory to the last
therapy received. All patients must have failed or ineligible to receive all therapies
with clinical benefit.
6. Adequate organ function:
- Measured or estimated creatinine clearance 50 mL/min by institutional standard
method
- AST or ALT 2.5 the upper limit of normal (ULN)
- Serum total bilirubin 1.5 ULN (or 3 ULN for patients with Gilbert syndrome)
- Ejection fraction =50%
7. Adequate BM function independent of growth factor or transfusion support, within 2
weeks of screening, unless cytopenia is clearly due to marrow involvement of B-ALL:
- Platelet count =50,000/mm3
- ANC =500/mm3
- Hemoglobin =9 g/dL
8. WBC =10 K/µL at Cycle 1 Day 1
9. For women of childbearing potential: Agreement to remain abstinent (refrain from
heterosexual intercourse) or use 2 adequate methods of contraception, including at
least 1 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),
90 days after the final dose mosunetuzumab. Women must refrain from donating eggs
during this same period.
A woman is considered to be of childbearing potential if she is postmenarchal, has not
reached a postmenopausal state ( 24 continuous months of amenorrhea with no identified
cause other than menopause), and is not permanently infertile due to surgery (i.e.,
removal of ovaries, fallopian tubes, and/or uterus) or another cause as determined by
the investigator (e.g., Müllerian agenesis). Even in presence of infertility history,
a reliable contraception, including 2 adequate methods of contraception, is indicated.
Examples of non-hormonal contraceptive methods with a failure rate of 1% per year
include bilateral tubal ligation, male sterilization, established and proper use of
progestogen only hormonal contraceptives that inhibit ovulation, hormone releasing
intrauterine devices, and copper intrauterine devices. Barrier methods must always be
supplemented with the use of a spermicide.
10. For men: Agreement to remain abstinent (refrain from heterosexual intercourse) or use
contraceptive measures and agreement to refrain from donating sperm, as defined below:
With female partners of childbearing potential or pregnant female partners, men must
remain abstinent or use a condom during the treatment period and for 90 days after the
final dose of mosunetuzumab. Men must refrain from donating sperm during this same
period.
Exclusion Criteria:
Patients who meet any of the following criteria will be excluded from study entry:
11. Active CNS disease. Previous history of CNS disease is allowed as long as last
documented CNS positivity is >3 months ago, and the last 2 LP are negative for CNS
leukemia.
12. Prior standard or investigational anti cancer therapy as specified below:
- Chimeric antigen receptor T cell therapy within 30 days prior to Day 1 of Cycle 1
- Monoclonal antibody or antibody drug conjugate within 4 weeks prior to Cycle 1
Day 1
- Treatment with any anti cancer agent (investigational or otherwise) within 4
weeks or 5 half-lives of the drug, whichever is shorter, prior to first dose of
study treatment
- Note: For urgent cytoreduction, steroids and hydroxyurea are permitted up to 2
days prior to Cycle 1 Day 1.
13. Clinically significant toxicity (other than alopecia) from prior treatment that has
not resolved to Grade 1 (per NCI CTCAE, v5.0) prior to Day 1 of Cycle 1
14. Treatment with systemic immunosuppressive medications, including, but not limited to,
prednisone ( 20 mg) within 2 weeks prior to Day 1 of Cycle 1
- The use of inhaled corticosteroids is permitted
- The use of mineralocorticoids for management of orthostatic hypotension is
permitted
- Single dose of dexamethasone for nausea or B symptoms is permitted
- Use of steroids for cytoreduction is permitted as per criteria above
15. History of solid organ transplantation
16. History of severe allergic or anaphylactic reaction to humanized, chimeric or murine
monoclonal antibodies (MAbs)
17. Known hypersensitivity to biopharmaceuticals produced in CHO cells or any component of
the mosunetuzumab, lenalidomide, or thalidomide formulation, including mannitol
18. History of erythema multiforme, Grade 3 rash, or blistering following prior treatment
with immunomodulatory derivatives
19. Active uncontrolled bacterial, viral, fungal, or other infection
20. Known or suspected chronic active Epstein-Barr virus (EBV) infection
21. Known or suspected history of hemophagocytic lymphohistiocytosis (HLH)
22. Clinically significant history of liver disease, including viral or other hepatitis,
or cirrhosis
23. Active Hepatitis B infection
- Patients who are hepatitis B surface antigen (HBsAg) negative and hepatitis B core
antibody (HBcAb) positive, must be negative for hepatitis B virus (HBV) polymerase
chain reaction (PCR) to be eligible for study participation
24. Active Hepatitis C infection
- Patients who are positive for hepatitis C virus (HCV) antibody must be negative for
HCV by PCR to be eligible for study participation
25. Known history of human immunodeficiency virus (HIV) positive status
- For patients with unknown HIV status, HIV testing will be performed at screening if
required by local regulations
26. History of progressive multifocal leukoencephalopathy (PML)
27. Administration of a live, attenuated vaccine within 4 weeks before first dose of study
treatment
28. Other malignancy that could affect compliance with the protocol or interpretation of
results, with the exception of the following:
- Any of the following malignancies previously curatively treated: carcinoma in
situ of the cervix, good-prognosis ductal carcinoma in situ of the breast, basal,
or squamous cell skin cancer
- Stage I melanoma, low grade, early stage localized prostate cancer, or any other
previously treated malignancy that has been in remission without treatment for 2
years prior to enrollment
29. Active autoimmune disease requiring treatment
30. History of autoimmune disease, including, but not limited to: myocarditis,
pneumonitis, myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus
erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis
associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's
syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or
glomerulonephritis
- Patients with a remote history of, or well-controlled autoimmune disease, with a
treatment free interval from immunosuppressive therapy for 12 months may be
eligible to enroll if judged to be safe by the investigator
- Patients with a history of autoimmune-related hypothyroidism on a stable dose of
thyroid-replacement hormone are eligible
- Patients with controlled Type 1 diabetes mellitus who are on an insulin regimen
are eligible for the study
- Patients with a history of disease-related immune thrombocytopenic purpura, or
autoimmune hemolytic anemia may be eligible
31. Evidence of any significant, uncontrolled concomitant disease that could affect
compliance with the protocol or interpretation of results, including, but not limited
to, significant cardiovascular disease (e.g., New York Heart Association Class III or
IV cardiac disease, myocardial infarction within the previous 6 months, unstable
arrhythmia, or unstable angina) or significant pulmonary disease (such as obstructive
pulmonary disease or history of bronchospasm)
32. Major surgical procedure within 28 days prior to Day 1 of Cycle 1
33. Pregnant or lactating or intending to become pregnant during the study Women of
childbearing potential must have negative serum/urine pregnancy test within 14 days
prior to initiating therapy
34. Any serious medical condition or abnormality in clinical laboratory tests that, in the
investigator's judgment, precludes the patient's safe participation in and completion
of the study, or which could affect compliance with the protocol or interpretation of
results
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