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Total Neoadjuvant Immunotherapy Plus Chemotherapy for Locally Advanced Gastric or Gastroesophageal Junction Adenocarcinoma (TNICE-1)

6 de noviembre de 2026 actualizado por: Beijing Tsinghua Chang Gung Hospital

A Multicenter, Prospective Study of Total Neoadjuvant Immunotherapy Combined With Chemotherapy in Patients With Locally Advanced Gastric or Gastroesophageal Junction Adenocarcinoma: The TNICE-1 Study

This study is for people with locally advanced adenocarcinoma of the stomach or of the junction between the stomach and esophagus (gastroesophageal junction adenocarcinoma) that can be removed by surgery. Serplulimab (an anti-PD-1 antibody) has been approved in China for use around the time of surgery in this type of cancer. This study will evaluate a treatment approach called total neoadjuvant therapy, in which all planned immunotherapy plus chemotherapy is given before surgery.

About 42 patients will take part at 2 hospitals in China. All participants will receive serplulimab plus the SOX regimen (oxaliplatin and S-1) before surgery, followed by surgical removal of the tumor. All treatment is given before surgery. After surgery, participants will not receive additional chemotherapy or immunotherapy. They will be followed regularly with examinations and tests to check for any return of the cancer.

Researchers will collect tumor tissue, blood, and stool samples before, during, and after treatment. These samples will be used to study how the tumor and the immune system change during treatment, including the immune cells inside the tumor, the tumor's genetic features, and traces of tumor DNA in the blood. Researchers will also grow mini-tumors (organoids) from patients' tumor tissue in the laboratory to test how the tumor responds to drugs.

The study will measure how completely the tumor shrinks or disappears after treatment, the side effects participants experience, and how long participants remain free of cancer after surgery. Participants will be followed regularly after treatment ends.

Descripción general del estudio

Descripción detallada

This is a multicenter, prospective clinical study of total neoadjuvant immunotherapy combined with chemotherapy in patients with locally advanced, resectable gastric or gastroesophageal junction adenocarcinoma. All participants receive a uniform regimen of the anti-PD-1 antibody serplulimab combined with the SOX regimen(oxaliplatin and S-1) administered entirely before surgery (total neoadjuvant approach), followed by radical gastrectomy. Unlike approved perioperative strategies in which immunotherapy is continued after surgery as maintenance monotherapy, this study administers the entire planned course of immunochemotherapy before surgery and does not administer any postoperative systemic therapy. The total neoadjuvant approach is intended to maximize treatment delivery while patients are treatment-naive and physiologically fit, to avoid postoperative complications delaying or preventing adjuvant therapy, and to allow pathological response at surgery to serve as an in vivo readout of treatment efficacy.

The study is embedded in a comprehensive translational research program. Longitudinal biospecimens (tumor tissue, peripheral blood, ascites if present, and stool) are collected at predefined time points. Exploratory research includes multiplex immunohistochemistry (mIHC), spatial transcriptomics, single-cell RNA sequencing, whole-exome sequencing, circulating tumor DNA (ctDNA)-based minimal residual disease (MRD) monitoring, patient-derived organoid (PDO) drug screening, gut microbiome profiling, and development of an artificial-intelligence-based model to predict treatment response. Because no postoperative therapy is administered, postoperative ctDNA-based MRD assessment is used for risk stratification and to inform individualized surveillance strategies. These analyses aim to identify biomarkers of response and resistance to total neoadjuvant immunochemotherapy and to support individualized perioperative treatment strategies.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

42

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Lingling Zhang
  • Número de teléfono: +86010-56111012
  • Correo electrónico: zlla05536@btch.edu.cn

Copia de seguridad de contactos de estudio

  • Nombre: Qiong Wu
  • Número de teléfono: +86010-56111011

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana
        • Reclutamiento
        • Beijing Tsinghua Changgung Hospital
        • Contacto:
    • Guangdong
      • Guangzhou, Guangdong, Porcelana
        • Aún no reclutando
        • Nanfang Hospital of Southern Medical University
        • Contacto:
          • Hao Liu
          • Número de teléfono: +86020-62787626
          • Correo electrónico: Andynf@smu.edu.cn

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Able to understand the study and provide signed informed consent (ICF)
  • Histologically confirmed adenocarcinoma of the stomach or gastroesophageal junction, clinically staged as stage II/III disease (cT1-2N+M0 or cT3-4aNxM0) based on contrast-enhanced CT/MRI
  • Willing to provide archived tumor tissue or undergo biopsy for central laboratory testing of PD-L1, EBV, and MSI/dMMR status
  • Tumor with PD-L1 CPS >=5, or MSI-H/dMMR, or EBV positivity
  • Male or female, age >=18 years
  • ECOG performance status 0-1, with no surgical contraindications
  • Life expectancy >=6 months
  • Laboratory values within 7 days prior to enrollment: absolute neutrophil count (ANC) >=1.5 x 10^9/L; platelet count >=100 x 10^9/L; hemoglobin >=90 g/L; serum albumin >=30 g/L; total bilirubin <=1.5 x ULN; AST and ALT <=2.5 x ULN (<=5 x ULN in subjects with liver metastases); creatinine <=1.5 x ULN or creatinine clearance >=50 mL/min; INR and aPTT <=1.5 x ULN (applicable only to subjects not receiving anticoagulant therapy; subjects receiving anticoagulants must be on a stable dose)
  • Good compliance and willingness to cooperate with protocol-required examinations and specimen collection (tissue, blood, stool, and saliva samples)
  • Women of childbearing potential must agree to use contraception from the time of ICF signing until at least 5 months after the last dose of study treatment or accompanying chemotherapy, and must not breastfeed; men must agree to use contraception from the first dose of study drug until at least 7 months after the last dose

Exclusion Criteria:

  • Known allergy to serplulimab or its excipients, oxaliplatin, or components of tegafur/gimeracil/oteracil potassium (S-1)
  • Prior or concurrent other malignancy (except adequately treated basal cell carcinoma of the skin or carcinoma in situ of the uterine cervix)
  • Uncontrolled pericardial effusion, pleural effusion, ascites, or gastrointestinal bleeding within 2 weeks prior to enrollment
  • Body weight loss >20% within 2 weeks prior to enrollment
  • Unable to take oral medications
  • Prior chemotherapy, radiotherapy, targeted therapy, immunotherapy, or surgery for gastric cancer
  • Prior treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibodies
  • HER2-positive tumor confirmed by central laboratory testing (IHC 3+, or IHC 2+ with positive FISH/ISH)
  • Comorbidities requiring long-term immunosuppressive therapy, or systemic or local corticosteroids at immunosuppressive doses
  • Vaccination with any anti-infectious vaccine within 4 weeks prior to enrollment
  • Uncontrolled diabetes mellitus, hypertension, or other systemic diseases
  • Currently receiving or requiring anticoagulant therapy (low-dose aspirin antiplatelet therapy allowed)
  • Any active autoimmune disease or history of autoimmune disease
  • Active tuberculosis, currently receiving anti-tuberculosis treatment, or anti-tuberculosis treatment within 1 year prior to screening
  • Confirmed interstitial pneumonitis, non-infectious pneumonitis, pulmonary fibrosis, or history of acute lung disease
  • Any contraindication to oxaliplatin or S-1
  • Pregnant or breastfeeding women
  • Active hepatitis (HBV DNA >=10^4 copies/mL or positive HCV RNA)
  • Positive HIV antibody or human T-lymphotropic virus type 1 (HTLV-1) antibody
  • Any other clinically significant disease or condition that, in the investigator's judgment, may affect protocol compliance or render the subject unsuitable for participation

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Serplulimab + SOX

All participants receive total neoadjuvant therapy consisting of serplulimab plus the SOX regimen administered entirely before surgery, followed by radical gastrectomy. No postoperative systemic therapy is administered.

Anti-PD-1 monoclonal antibody administered as neoadjuvant immunotherapy in combination with the SOX regimen, given entirely before surgery (total neoadjuvant approach).

Combination chemotherapy of oxaliplatin plus S-1 (tegafur/gimeracil/oteracil), administered before surgery in combination with serplulimab.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Pathological Complete Response (pCR) Rate
Periodo de tiempo: At surgery (approximately 6 months after start of study treatment)

Proportion of participants achieving pathological complete response, defined as no viable tumor cells in the resected primary tumor and lymph nodes (ypT0 ypN0), assessed by local pathology review of the surgical specimen.

At surgery (approximately 6 months after start of study treatment)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Colaboradores

Investigadores

  • Investigador principal: Guoxin Li, Department of General Surgery, Cancer Center, Beijing Tsinghua Changgung Hospital

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

5 de agosto de 2026

Finalización primaria (Estimado)

30 de diciembre de 2027

Finalización del estudio (Estimado)

30 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

6 de noviembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de noviembre de 2026

Publicado por primera vez (Actual)

12 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

6 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

Individual participant data (IPD) that underlie the results reported in this study, after deidentification (text, tables, figures, and appendices), will be shared. Deidentified IPD will be made available beginning 9 months after primary completion of the study and will remain available for 5 years. Data will be shared with qualified investigators worldwide who submit a methodologically sound proposal for secondary analyses, such as individual participant data meta-analysis; proposals may be submitted at any time while the data are available. Data will be provided upon reasonable request approved by the study team, together with a signed data access agreement, through secure data transfer. The study protocol and statistical analysis plan will also be available upon request under the same terms. No re-identification of participants is permitted.

Marco de tiempo para compartir IPD

eidentified individual participant data and supporting information (study protocol and statistical analysis plan) will be available beginning 9 months after the primary completion date of the study and will remain available for 5 years thereafter.

Criterios de acceso compartido de IPD

Qualified investigators affiliated with academic or research institutions may request access to the deidentified individual participant data that underlie the results reported in this study, as well as the study protocol and statistical analysis plan. Requests must include a methodologically sound research proposal and a signed data access agreement, and will be reviewed by the study team. Approved data will be provided through secure data transfer. Re-identification of study participants is not permitted. Requests may be submitted at any time while the data are available.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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