Anti-CD7 Allogeneic CAR T-Cells (WU-CART-007) in Treating Patients with CD7+ Hematologic Cancers

Inclusion Criteria

• COHORT A
• Patients will have T-cell non-Hodgkin lymphoma with relapsed or refractory disease defined as one of the following: * Relapsed or refractory after at least 2 or more prior lines of therapy (for patients with anaplastic large cell lymphoma, they must have prior therapy brentuximab vedotin). For patients with T-PLL, only 1 or more prior line of therapy is required. OR * Relapsed after autologous or allogeneic hematopoietic cell transplant
• Permissible T-cell NHL subtypes will include: * Angioimmunoblastic T-cell lymphoma (AITL) * Enteropathy-associated T-cell lymphoma (EATL) * Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) * Peripheral T-cell lymphoma (PTCL) NOS * Anaplastic large cell lymphoma (ALCL) * Adult T-cell leukemia/lymphoma * T-cell prolymphocytic leukemia (T-PLL) * Extranodal NK/T cell lymphoma * Transformed mycosis fungoides/Sezary Syndrome * Primary cutaneous gamma/delta T-cell lymphoma * Hepatosplenic T cell lymphoma
• COHORT B
• Patients will have acute myeloid leukemia (AML) (acute leukemia of ambiguous lineage may be enrolled and treated per AML cohort) with relapsed or refractory disease unlikely to benefit from standard therapy defined as one of the following: * Primary refractory AML defined as: ** Minor or no response to intensive induction chemotherapy with more than 15% blasts and less than 50% proportional reduction in blast percentage after C130, OR ** Absence of morphological CR/CRi following either: *** >= 2 cycles of intensive induction chemotherapy *** >= 2 cycles of HMA plus venetoclax, or *** >= 4 total cycles of an HMA OR ** Morphologic relapse (>= 5% bone marrow blasts) with either: *** Initial CR duration < 1 year, OR *** Prior unsuccessful salvage attempt or allogeneic HCT, OR *** 2nd relapse or higher OR ** Disease progression while on treatment with HMA+/-venetoclax for MDS/AML
• Patients with a susceptible FLT3, IDH1 or IDH2 mutation should be resistant or intolerant to an agent targeting the specific mutation or otherwise be determined to be ineligible to receive a targeted agent by their treating physician
• Circulating blast count must be < 30,000/uL by morphology or flow cytometry (cytoreductive therapies including leukapheresis or hydroxyurea are allowed)
• BOTH COHORTS
• CD7 positive expression must be demonstrated in malignant cells in bone marrow, peripheral blood, or lymph node biopsies (fresh or archival) by Washington University Pathology lab. For both dose escalation (Part A) and dose expansion (Part B), any qualitative expression of CD7 will be permitted
• Age >= 18 years of age
• Eastern Cooperative Oncology Group performance status =< 2
• Total bilirubin =< 2x upper limit of normal (ULN) (unless the patient has grade 1 bilirubin elevation due to Gilbert's disease or a similar syndrome involving slow conjugation of bilirubin)
• Aspartate transaminase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine transaminase (ALT) (serum glutamate-pyruvate transaminase [SGPT]) =< 5x ULN
• Creatinine within normal institutional limits OR creatinine clearance >= 30 mL/min/1.73 m^2 by Cockcroft-Gault Formula
• Oxygen saturation >= 90% on room air
• Ejection fraction >= 40% confirmed by echocardiogram or MUGA
• For T-NHL patients with bone marrow involvement and AML patients, no hematologic parameters are required. For T-NHL patients without bone marrow involvement, adequate hematologic parameters are required, including: * Hemoglobin >= 8 g/dL without transfusion within 7 days * Platelets >= 20,000 / uL without transfusion within 7 days * Absolute neutrophil count >= 500 / uL
• The effects of WU-CART-007 on the developing human fetus are unknown. For this reason, women of childbearing potential and male patients (along with their female partners) are required to use two forms of acceptable contraception, including one barrier method, during participation in the study and for 12 months following the last dose of WU-CART-007. Should a woman (or the female partner of a male patient) become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately
• Patients must have no other effective standard of care therapy options, and patients must be unwilling or unable to travel to another site for treatment
• DOSE ESCALATION ONLY: The patient must be considered a candidate for allogeneic hematopoietic stem cell transplantation in the opinion of the treating physician, and an acceptable allogeneic hematopoietic stem cell donor must be identified prior to study enrollment in case a patient experiences toxicity post-infusion that necessitates rescue HSCT. The identified donor may be related, unrelated, haplo-identical or umbilical cord blood, and does not need to be medically cleared prior to screening or dosing. If none of the patients at the RP2D experience severe recurrent infections due to prolonged lymphopenia or otherwise require rescue HSCT (excluding elective HSCT due to treating physician’s choice for treatment of underlying disease), subsequent patients will not require identification of a donor prior to enrollment in dose expansion
• Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document

Exclusion Criteria

• Received systemic anticancer therapy (including investigational therapy) or radiotherapy < 28 days or 5 half-lives, whichever is shorter, prior to the start of lymphodepleting chemotherapy with the exception of bridging treatment
• Received any T-cell lytic or toxic antibody (e.g., alemtuzumab) within 8 weeks prior to lymphodepleting chemotherapy
• Subjects who have received a prior allogeneic HCT are excluded if any of the following criteria are present: * < 100 days post alloHCT * < 6 weeks from prior donor leukocyte infusion * Presence of acute or extensive chronic GVHD requiring systemic immunosuppression except for prednisone =< 10 mg or equivalent. * < 28 days from last dose of systemic immunosuppressive therapy (eg. calcineurin inhibitors, immunosuppressive antibodies, mycophenolate mofetil, ruxolitinib, ibrutinib) except for prednisone =< 10 mg or equivalent
• Previous treatment with any anti-CD7 directed therapy
• Known hypersensitivity to one or more of the study agents
• Active or latent hepatitis B or active hepatitis C without previous curative treatment
• Confirmed human immunodeficiency virus (HIV) infection
• History of concurrent second cancers requiring active, ongoing systemic treatment with the exception of adjuvant hormonal therapy for breast or prostate cancer
• Pregnant and/or breastfeeding. Women of childbearing potential must have a negative serum or urine pregnancy test at time of enrollment and within 7 days of starting lymphodepleting chemotherapy
• Serious active infection or another serious underlying medical condition that in the opinion of the treating physician would impair the ability of the patient to receive protocol treatment including, but not limited to symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardiac arrhythmia or serious, unstable neurologic symptoms
• Symptomatic, uncontrolled hypotension