TROP2-CAR-NK cells in Combination with Cetuximab for the Treatment of Colorectal Cancer in Patients with Minimal Residual Disease

Inclusion Criteria

• Patients must be 18 years or older
• Patients must be willing and able to provide informed consent
• Willing and able to comply with clinical trial instructions and requirements. Individuals lacking the ability, based on reasonable medical judgment, to understand and appreciate the nature and consequences of participation in this study will not be eligible for participation
• In both the dose escalation and dose expansion cohorts, patients must have documented colorectal cancer (CRC) with MRD following complete disease resection followed by standard-of-care adjuvant treatment. MRD is defined as NO evidence of radiological disease (including patients with undefinable lesion with max diameter < 1 cm or with a short axis < 1cm for lymph nodes) and presence of circulating ctDNA in the bloodstream
• Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• Life expectancy > 3 months
• A female patient is eligible to participate if at least one of the following conditions applies: * Not a woman of childbearing potential (WOCBP) OR * A WOCBP who agrees to follow the contraceptive guidelines during the study treatment period and for 6 months post TROP2-CAR-NK cell infusion
• Female patients who become pregnant or suspect pregnancy must immediately notify their doctor. Female patients who become pregnant will be taken off study
• Male patients must agree to follow the contraceptive guidelines during the study treatment period and for 6 months post TROP2-CAR-NK cell infusion. Male patients who father a child or suspect that they have fathered a child must immediately notify their doctor
• WOCBP must have a negative urine pregnancy test within 72 hours prior to the start of lymphodepleting chemotherapy. If a WOCBP has a urine pregnancy test that cannot be confirmed as negative, a serum (beta human chorionic gonadotropin [beta-hCG]) pregnancy test will be required
• Absolute neutrophil count (ANC) ≥ 1500/uL (within 10 days prior to the start of lymphodepleting chemotherapy)
• Platelets ≥ 100,000/uL (within 10 days prior to the start of lymphodepleting chemotherapy)
• Hemoglobin ≥ 9.0 g/dL (within 10 days prior to the start of lymphodepleting chemotherapy); Note: Criteria must be met without erythropoietin dependency and without packed red blood cell transfusion within last 2 weeks of the screening test. Patients may be on a stable dose of erythropoietin ( ≥ approximately 3 months)
• Creatinine clearance (CrCl) by Cockcroft-Gault formula ≥ 45 mL/min for patients with creatinine > 1.5 × upper limit of normal (ULN) (within 10 days prior to the start of lymphodepleting chemotherapy); Note: Serum creatinine and CrCl should be interpreted and calculated per institutional standard
• Total bilirubin ≤ 1.5 × ULN OR direct bilirubin ≤ ULN for patients with total bilirubin levels > 1.5 × ULN (within 10 days prior to the start of lymphodepleting chemotherapy)
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN ( ≤ 5 × ULN for patients with history of resected liver metastases) ( within 10 days prior to the start of lymphodepleting chemotherapy)
• Prothrombin time (PT)/international normalized ratio (INR) activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN unless patient is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants (within 10 days prior to the start of lymphodepleting chemotherapy)
• Left ventricular ejection fraction (LVEF) > 50%. Of note, those patients with risk factors and/or with LVEF <55% additional testing may need to be performed as per institutional guidelines and/or principal investigator (PI) guidance
• Adequate respiratory reserve defined as dyspnea grade 0 or 1 and saturated oxygen > 92% in room air
• Willing to undergo mandatory blood collections and biopsies as required by the study
• Willing to stay within a 2-hour drive (approximately 100-mile radius) of the study site during the first 4 weeks after the TROP2-NK cell infusion

Exclusion Criteria

• Patients with known active disease by Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1
• Pregnant, breastfeeding, or expecting to conceive within the projected duration of the study, starting with the screening visit through 6 months post TROP2-CAR-NK cell infusion
• Has received systemic anticancer therapy within 2 weeks or 3 half-lives, whichever is shorter, prior to the start of lymphodepleting chemotherapy. For patients treated with monoclonal antibodies, at least 3 weeks must have elapsed prior to the start of lymphodepleting chemotherapy. Patients who have entered the follow-up phase of an investigational study may participate as long as it has been 3 weeks after the last dose of the previous investigational agent
• Patients must have recovered from all adverse events (AEs) due to previous therapies to ≤ grade 1 or baseline. Patients with ≤ grade 2 neuropathy, alopecia, or other non-relevant AEs may be deemed eligible at the discretion of the principal investigator (PI). If a patient received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to the start of lymphodepleting chemotherapy
• Has received prior radiotherapy within 2 weeks of the start of lymphodepleting chemotherapy. Patients must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis or colitis
• Has received a live vaccine within 6 weeks prior to TROP2-CAR-NK infusion and for at least 24 months post infusion. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette–Guérin, and typhoid vaccine. Seasonal influenza and COVID-19 vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist registered trademark) are live attenuated vaccines and are not allowed
• Prior genetically modified T or NK cell therapy
• Has diagnosis of immunodeficiency or receiving chronic systemic steroid therapy (in doses exceeding 10 mg daily of prednisone equivalent)
• History of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 2 years. The time requirement does not apply to patients who underwent successful definitive resection of basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, in situ cervical cancer, or other in situ cancers
• Active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease-modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is allowed
• History of interstitial lung disease (ILD) that required steroids or has current pneumonitis/ILD
• Active infection requiring systemic therapy
• Known human immunodeficiency virus (HIV) infection
• Known active or chronic hepatitis B or hepatitis C virus infection
• Known history of active tuberculosis (Mycobacterium Tuberculosis)
• History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the patient’s participation for the full duration of the study, or is not in the best interest of the patient to participate, in the opinion of the treating investigator
• Known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the study
• Has had an allogenic tissue/solid organ transplant
• Clinically significant cardiovascular disease within 12 months prior to the start of lymphodepleting chemotherapy, including New York Heart Association Class III or IV congestive heart failure, unstable angina, myocardial infarction, cerebrovascular event, or cardiac arrhythmia associated with hemodynamic instability. NOTE: medically controlled arrhythmia would be permitted if meet criteria
• Prolongation of corrected QT interval using Fridericia’s formula to > 480 milliseconds, unless cleared after cardiology evaluation
• Patients with bleeding or thrombotic disorders or at risk for severe hemorrhage. Patients with known deep vein thrombosis/pulmonary embolism who are on appropriate anti-coagulation treatment are eligible