A Study of Mesothelin-Targeted CAR T-Cell Therapy in People With Esophagogastric Cancer

{ "Mesothelin-Targeted CAR T-Cell Therapy for Esophagogastric Cancer", "This study is testing a new type of cell therapy called M28z1XXPD1DNR CAR T-cells for people with esophagogastric (a type of stomach and esophagus) cancer that has spread or come back. This therapy uses your own immune cells (T-cells) that are specially changed in a lab to find and fight cancer cells that have a marker called mesothelin. Researchers want to see how safe this treatment is and find the right dose. To join, you must be at least 18 years old, have confirmed esophagogastric adenocarcinoma that is metastatic or recurrent, and have a good enough health status (ECOG performance status of 0-1). Your T-cells will be collected through a procedure called leukapheresis, and the study therapy will take about 3-4 weeks.", "design": "This is an interventional study with a planned enrollment of 18 participants. The phase of the study is not specified.", "commitments": "You will have your white blood cells (T-cells) collected through a procedure called leukapheresis. The study therapy, which involves receiving the modified T-cells, will take about 3-4 weeks.", "compensation": "Not stated in the trial record.", "follow_up": "Researchers will monitor you for treatment-related side effects and the maximum tolerated dose for up to one year after treatment.", }

Study design
Not specified.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Not specified.

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NCT06623396

A Study of Mesothelin-Targeted CAR T-Cell Therapy in People With Esophagogastric Cancer

Recruiting
PHASE1Ages 18+InterventionalTreatment
Memorial Sloan Kettering Cancer Center
~18 participants
Updated 2026-02-11 on ClinicalTrials.gov
What's tested:M28z1XXPD1DNR CAR

At a glance

Recruiting sites
7 of 7 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of treatment-emergent adverse events
Measured over 1 year
+1 more outcome measured
Mesothelin Positive
Mesothelin-Expressing Tumors
Esophageal Adenocarcinoma
Esophageal Adenocarcinomas
Esophagogastric Adenocarcinoma
Peritoneal Carcinomatosis
Breast Neoplasms
Diabetes Mellitus
7 sites across 2 states
New York4
New Jersey3
  • Geoffrey Ku, MD · PRINCIPAL_INVESTIGATOR · Memorial Sloan Kettering Cancer Center

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Eligibility criteria

Inclusion

Aged ≥18 years
Diagnosis of pathologically confirmed EG adenocarcinoma
Diagnosis of metastatic or recurrent disease
ECOG performance status of 0-1
Life expectancy of ≥4 months
Written informed consent for the study (from participant)
Life expectancy of ≥4 months
ECOG performance status of 0-1
Histologic diagnosis that \& \>25% of the tumor expresses MSLN by IHC analysis. Archival tissue obtained up to 2 years before study enrollment is acceptable. IHC testing of a cell block from cytology (e.g., ascitic fluid) is acceptable if approved by the study pathologist. If adequate archival tissue is not available at screening, a fresh tumor biopsy should be obtained
Stage IV disease with gross peritoneal carcinomatosis on imaging and/or microscopic peritoneal involvement by cytology or noted during diagnostic laparoscopy
Disease progression or treatment intolerance after receiving at least 1 treatment regimen in the metastatic setting; patients with disease recurrence within 6 months of completing curative systemic therapy (chemotherapy, chemoradiation or adjuvant immunotherapy) are also eligible
Patients with Her2 positive disease must have received ≥1 line of anti-Her2 based therapy
At least 1 measurable or evaluable lesion per RECIST 1.1. Screening imaging must be obtained within 6 weeks of signing the informed consent form
Completion of systemic therapy at least 7 days before leukapheresis
Lab requirements (hematology):
Absolute neutrophil count ≥1.0 K/mcL
Hemoglobin ≥9 gm/dL
Platelet count ≥75 K/mcL
Blood product transfusion or growth factor support cannot occur within 7 days of testing
Lab requirements (serum chemistry):
Bilirubin ≤1.5× upper limit of normal (ULN)
Serum alanine aminotransferase and serum aspartate aminotransferase (ALT/AST) level ≤3× ULN
Calculated clearance of ≥50 mL/min by Cockcroft-Gault equation
Negative screen for infectious disease markers, including hepatitis B core antibody, hepatitis B surface antigen, hepatitis C antibody, HIV 1-2 antibody, HTLV antibody and syphilis antibody
Serum pregnancy test with negative result at screening and preconditioning and must be willing to use effective and reliable contraception for at least 12 months after T cell infusion (for female participants of childbearing age)
Resolution of all acute toxic effects of any previous therapeutic or palliative chemotherapy, radiotherapy, or surgical procedures to grade ≤1 (CTCAE v5.0), except for neuropathy and alopecia
Life expectancy of ≥4 months
ECOG performance status of 0-1
At least 1 measurable or evaluable lesion per RECIST 1.1. Screening imaging must be obtained within 4 weeks before the date of lymphodepletion
Completion of systemic therapy at least 14 days before lymphodepleting chemotherapy
Lab requirements (hematology):
Absolute neutrophil count ≥1.5 K/mcL
Hemoglobin ≥8 gm/dL
Platelet count ≥75 K/mcL
Lab requirements (serum chemistry):
Bilirubin ≤1.5× upper limit of normal (ULN)
Serum alanine aminotransferase and serum aspartate aminotransferase (ALT/AST) level ≤3× ULN
Calculated clearance of ≥50 mL/min by Cockcroft-Gault equation
Serum pregnancy test with negative result within 7 days of planned lymphodepletion date and must be willing to use effective and reliable contraception for at least 12 months after T cell infusion (for female participants of childbearing age)
Resolution of all acute toxic effects of any previous therapeutic or palliative chemotherapy, radiotherapy, or surgical procedures to grade ≤1 (CTCAE v5.0), except for neuropathy and alopecia

Exclusion

Pregnant or lactating
HIV, active hepatitis C virus, or active hepatitis B virus infection, as determined by quantitative PCR (patients who have undergone negative testing prior to leukapheresis do not require repeat testing)
Receiving therapy for concurrent active malignancy
Note: Patients receiving treatment for in situ skin malignancies are not excluded.
Patients with any malignancy diagnosed \>3 years before that is thought to be curatively treated and/or has a low risk of recurrence are eligible. Patients may continue to receive adjuvant therapy at the time of study enrollment (e.g., adjuvant hormonal therapy for curatively treated breast cancer).
Known hematologic malignancy requiring treatment in the preceding 5 years or a known history of lymphoid malignancy
Previous receipt of CAR T cell therapy or any other cellular therapy
Previous mesothelin-directed therapy Any major abdominal surgery (laparotomy with resection of gastrointestinal tract or organ resection) that is completed \<28 days before study enrollment. Patients who have undergone diagnostic laparoscopy can be included in the study without regard to timing
Untreated or active central nervous system (CNS) metastases (progressing or requiring anticonvulsants or corticosteroids for symptomatic control). Patients with a history of treated CNS metastases are eligible if all of the following criteria are met:
Radiographic demonstration of improvement upon completion of CNS-directed therapy and no evidence of interim progression between completion of CNS-directed therapy and the screening radiographic study
Completion of radiotherapy ≥4 weeks before the screening radiographic study
Active autoimmune disease that has required systemic treatment within 1 year before leukapheresis (with the use of disease-modifying agents, corticosteroids, or immunosuppressive drugs)
Receiving daily systemic corticosteroids ≥10 mg of prednisone daily or equivalent or receiving immunosuppressive or immunomodulatory treatment
Any of the following cardiac conditions:
New York Heart Association stage III or IV congestive heart failure
Myocardial infarction ≤6 months before enrollment
History of myocarditis
Serious uncontrolled cardiac arrhythmia, unstable angina, or uncontrolled infection
Left ventricular ejection fraction ≤40%
Active interstitial lung disease/pneumonitis or a history of interstitial lung disease/pneumonitis requiring treatment with systemic steroids
Baseline pulse oximetry \<90% on room air at the screening time point
Known active infection requiring antibiotic treatment 7 days before leukapheresis
Any other medical condition, e.g. fever \>38.0 degrees C, that, in the opinion of the PI, may interfere with the subject's participation in or compliance with the study
Receipt of live, attenuated vaccine within 8 weeks before the planned lymphodepleting chemotherapy date
Deemed to be noncompliant by the study team for administration of a high-risk treatment agent and for close follow-up after treatment as required by the protocol
  • Number of treatment-emergent adverse events1 year

    The primary objective of this study is to assess the safety of M28z1XXPD1DNR CAR T cells administered through the peritoneal cavity. CTCAE v5.0 will be used to assess the severity of all treatment-emergent toxicities and adverse events, regardless of reporting requirements

  • Maximum Tolerated Dose of M28z1XXPD1DNR CAR T cellsUp to 1 year

    Determine the maximum tolerated dose of M28z1XXPD1DNR CAR T cells administered through the peritoneal cavity.