| Eligibility |
Inclusion Criteria:
- Age 18-69 years
- Confirmed Systemic Lupus Erythematosus (SLE) as per Systemic Lupus International
Collaborating Clinics (SLICC) 2012 Criteria with one or more of the following:
a. Active disease despite use of standard therapy (i) and one or more additional
therapies (ii).
i. Corticosteroids (CS), Hydroxychloroquine ii. Mycophenolate mofetil (MMF),
Methotrexate (MTX), Azathioprine (AZA), Tacrolimus (TAC), Cyclophosphamide (CYC),
Rituximab, and/or belimumab b. Active disease due to intolerance of standard therapy
(i) and one or more additional therapies (ii).
c. Steroid-Dependent Disease
- Subjects must meet organ function criteria:
1. Creatinine clearance more than or equal to 30 ml/min calculated by the Cockcroft
- Gault formula
2. Subjects must have adequate cardiac function as defined as left ventricular
ejection fraction = 40% on the most recent echocardiogram.
3. Adequate pulmonary function with pulse oximetry =92% on room air
4. Total Bilirubin = 1.5x the institutional upper limit of normal (except in
patients with Gilbert's syndrome)
5. ALT (SGPT) and AST (SGOT) < 3x the institutional upper limit of normal
Exclusion Criteria:
- SLE complicated by:
- Active neuropsychiatric lupus
- Active secondary hemophagocytic lymphohistiocytosis (sHLH)
- Presence of any medical or psychological conditions which may affect patient ability
to comply with study protocol requirements and study visits
- Presence of active, untreated infection such as:
- Active microbial infection. Patients with possible fungal infections must have
had at least 2 weeks of appropriate anti-fungal therapy and be asymptomatic.
Patients with active tuberculosis must have had at least 4 weeks of appropriate
anti-mycobacterial treatment and be asymptomatic.
- Active or latent hepatitis B or active hepatitis C (test within 8 weeks of
screening), or any uncontrolled infection at screening
- HIV positive test within 8 weeks of screening
- Acute/ongoing neurologic toxicity > Grade 1 except for a history of controlled
seizures or fixed neurologic deficits that have been stable/improving over the past 1
months.
- Patients with concomitant genetic syndrome: such as patients with Fanconi anemia,
Kostmann syndrome, Shwachman syndrome or any other known bone marrow failure syndrome.
Patients with Down Syndrome will not be excluded.
- Evidence of myelodysplasia or cytogenetic abnormality indicative of myelodysplasia on
any bone marrow biopsy prior to initiation of therapy
- Pregnant or breastfeeding women are excluded from this study because CAR-T cell
therapy may be associated with the potential for teratogenic or abortifacient effects.
Women of childbearing potential must have a negative serum pregnancy test. Because
there is an unknown, but potential risk for adverse events in nursing infants
secondary to treatment of the mother with CAR-T cells, breastfeeding should be
discontinued. These potential risks may also apply to other agents used in this study.
Women of childbearing potential must agree to remain abstinent (refrain from
heterosexual intercourse) or use a contraceptive method with a failure rate of < 1%
per year during the treatment period and for at least 6 months after the CAR-T cell
infusion.
- A woman is considered to be of childbearing potential if she is postmenarcheal, has
not reached a postmenopausal state (< 12 continuous months of amenorrhea with no
identified cause other than menopause), and has not undergone surgical sterilization
(removal of ovaries and/or uterus).
- Examples of contraceptive methods with a failure rate of < 1% per year include
bilateral tubal ligation, male sterilization, hormonal contraceptives that inhibit
ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices.
Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation
methods) and withdrawal are not acceptable methods of contraception.
- Men who will not agree to remain abstinent (refrain from heterosexual intercourse) or
use contraceptive measures, and agree to refrain from donating sperm, as defined
below:
- With female partners of childbearing potential, men must remain abstinent or use a
condom plus an additional contraceptive method that together result in a failure rate
of < 1% per year during the treatment period and for at least 6 months after the CAR-T
cell infusion. Men must refrain from donating sperm during this same period.
- With pregnant female partners, men must remain abstinent or use a condom during the
treatment period and for at least 6 months after the CAR- T cell infusion to avoid
potential embryonal or fetal exposure. The reliability of sexual abstinence should be
evaluated in relation to the duration of the clinical trial and the preferred and
usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation,
symptothermal, or postovulation methods) and withdrawal are not acceptable methods of
contraception.
- Patients receiving a live vaccines within the last two weeks.
- A minimum of 28 days must have elapsed between prior treatment with investigational
agent(s) and the day of lymphocyte collection.
- Concurrent use of high dose systemic steroids and/or T cell directed immune
suppression. Subjects must discontinue T cell targeted therapy >3 weeks and wean
prednisone dose to =10 mg/day prior to leukapheresis.
- Previous treatment with any gene or adoptive cell therapy products.
- Any serious, uncontrolled diseases (including, but not limit to, unstable angina
pectoris, congestive heart failure, serious arrhythmia, HIV, seizure disorder,
cerebrovascular disease, psychiatric disease), that may interfere with the patient's
ability to tolerate the therapy or comply with assessments.
- Active malignancy, other than non-melanoma skin cancer or carcinoma in situ (e.g.
cervix, bladder, breast). Patients with a prior or concurrent malignancy whose natural
history or treatment does not have the potential to interfere with the safety or
efficacy assessment of the investigational regimen are eligible for this trial (e.g.
Low Gleason score prostate Cancer).
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