CEA-Pozitif İlerlemiş Solid Tümörlerde CEA Hedefli CAR-T Tedavisi

Sade dilde özet

Bu Faz 1 (Phase 1), tek kollu ve açık etiketli çalışmada, doz artırımı ve doz genişletme aşamalarıyla CEA hedefli CAR-T hücre ürününün güvenliği ve etkinliği değerlendiriliyor. Çalışma ayrıca hücrelerin vücuttaki davranışını (farmakokinetik) inceleyerek önerilen dozu ve infüzyon programını belirlemeyi amaçlıyor. Katılımcılar, standart tedavilerden yarar görmemiş, 18 yaş ve üzeri, doku incelemesiyle doğrulanmış ilerlemiş, metastatik veya nükseden kanseri olan (başlıca kolorektal, yemek borusu, mide, pankreas, akciğer ve safra yolu kanserleri) hastalardır.

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

Faz 1 (Phase 1)

Durum

Katılımcı alıyor

Sponsor

Chongqing Precision Biotech Co., Ltd

Müdahale

CEA-targeted CAR-T cells, CEA-targeted CAR-T cells, CEA-targeted CAR-T cells

Başlangıç

12.09.2025

Tahmini bitiş

31.05.2028

Ülkeler

China

İlgili genler

Merkezler

• Hefei, China

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

Inclusion Criteria:

1. Age ≥ 18 years, no gender restriction;
2. Histopathologically confirmed diagnosis of advanced, metastatic, or recurrent malignant tumors, primarily including colorectal cancer, esophageal cancer, gastric cancer, pancreatic cancer, lung cancer, and cholangiocarcinoma;
3. Failure of at least second-line standard treatment (disease progression or intolerance, such as surgery, chemotherapy, radiotherapy, etc.) or lack of effective treatment options;
4. Immunohistochemical staining of tumor samples showing CEA positivity (clear membrane staining, positivity rate ≥ 10%) within the past 3 months; if the immunohistochemical result is older than 3 months (clear membrane staining, positivity rate ≥ 10%), serum CEA must exceed 10 µg/L;
5. At least one evaluable lesion according to RECIST 1.1 criteria;
6. ECOG performance status of 0-2;
7. Expected survival of ≥ 12 weeks;
8. No severe psychiatric disorders;
9. Unless otherwise specified, the following important organ function criteria must be met:

   1. Hematology: White blood cells \> 2.0 × 10\^9/L, neutrophils \> 0.8 × 10\^9/L, lymphocytes \> 0.5 × 10\^9/L, platelets \> 50 × 10\^9/L, hemoglobin \> 90 g/L;
   2. Cardiac function: Echocardiogram shows ejection fraction ≥ 50%, ECG shows no significant abnormalities;
   3. Renal function: Serum creatinine ≤ 2.0 × ULN;
   4. Liver function: ALT and AST ≤ 3.0 × ULN (can be relaxed to ≤ 5.0 × ULN for patients with liver tumor infiltration);
   5. Total bilirubin ≤ 2.0 × ULN;
   6. Oxygen saturation \> 92% without supplemental oxygen;
10. Eligible for single or venous blood collection, and no contraindications for cell collection;
11. The subject agrees to use reliable and effective contraception methods from the time of signing the informed consent form until 1 year after CAR-T cell infusion (excluding rhythm method);
12. The subject or their authorized guardian agrees to participate in this clinical trial and signs the informed consent form (ICF), indicating understanding of the trial's purpose and procedures and willingness to participate in the study.

Exclusion Criteria:

1. Clinically symptomatic central nervous system metastasis or meningeal metastasis at screening, or other evidence indicating that central nervous system or meningeal metastasis has not been controlled, as determined by the investigator, making the patient unsuitable for enrollment.
2. Participation in another clinical trial within 1 month prior to screening.
3. Receipt of live attenuated vaccines within 4 weeks prior to screening.
4. Received the following anti-tumor treatments within 14 days or at least 5 half-lives (whichever is shorter) prior to screening: chemotherapy, targeted therapy, or other experimental drug treatments.
5. Active infection requiring systemic treatment or an uncontrolled infection.
6. Bowel obstruction, active gastrointestinal bleeding, or a history of major gastrointestinal bleeding within the last 3 months, or severe gastrointestinal conditions such as severe gastric or duodenal ulcers, severe ulcerative colitis, or other severe gastrointestinal inflammations.
7. Toxicity from prior anti-tumor treatments has not improved to baseline levels or ≤ grade 1, except for alopecia or peripheral neuropathy.
8. Any of the following cardiac conditions:

   1. New York Heart Association (NYHA) Class III or IV congestive heart failure;
   2. Myocardial infarction or coronary artery bypass graft (CABG) within 6 months prior to enrollment;
   3. Clinically significant ventricular arrhythmias, or history of unexplained syncope (excluding cases due to vasovagal or dehydration);
   4. Severe non-ischemic cardiomyopathy.
9. Active autoimmune diseases or other conditions requiring long-term use of immunosuppressive therapy.
10. History of another malignancy within the past 3 years, excluding treated and stable in situ cervical cancer or basal cell carcinoma of the skin.
11. Positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) with peripheral blood hepatitis B virus (HBV) DNA levels above the normal range; positive for hepatitis C virus (HCV) antibodies with peripheral blood HCV RNA levels above the normal range; positive for HIV antibodies; or positive for syphilis testing.
12. Pregnant or breastfeeding women.
13. Any other conditions that, in the opinion of the investigator, make the patient unsuitable for participation in the study.