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Short-Course Online Adaptive Radiotherapy Combined With Chemotherapy, Targeted Therapy and Immunotherapy as Total Neoadjuvant Therapy (TNT) for Locally Advanced Rectal Cancer

14 de mayo de 2026 actualizado por: Dai, Guanghai, Chinese PLA General Hospital

A Single-Arm, Phase 2 Clinical Study on the Efficacy and Safety of Short-Course Online Adaptive Radiotherapy Combined With Chemotherapy, Targeted Therapy and Immunotherapy as Total Neoadjuvant Therapy (TNT) for Locally Advanced Rectal Cancer

Standard treatment for patients with proficient mismatch repair (pMMR) / microsatellite stable (MSS) locally advanced rectal cancer (LARC) consists primarily of neoadjuvant chemoradiotherapy followed by radical surgery. Several studies (including the UNION, STELLAR, TORCH, and SPRING-01 trials, etc) have demonstrated that the neoadjuvant strategy of short-course radiotherapy followed by chemotherapy combined with immunotherapy can improve pCR rate in patients with pMMR/MSS LARC, and might also provide higher organ preservation rates and long-term survival benefits. The study aims to explore the efficacy and safety of a TNT regimen comprising short-course radiotherapy combined with chemotherapy, cetuximab N01 (for patients with wild-type RAS/BRAF) or bevacizumab (for patients with mutant RAS/BRAF), and sintilimab in patients with high-risk LARC.

Descripción general del estudio

Estado

Aún no reclutando

Tipo de estudio

Intervencionista

Inscripción (Estimado)

60

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: Guanghai Dai, MD
  • Número de teléfono: +86 13801232381
  • Correo electrónico: 463043539@qq.com

Ubicaciones de estudio

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

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Voluntarily signed the informed consent form.
  • Aged 18-75 years (inclusive of 18 and 75 years).
  • pMMR/MSS.
  • Middle or low rectal cancer located ≤10 cm from the anal verge as assessed by MRI.
  • Histopathologically confirmed locally advanced rectal adenocarcinoma and high-risk features confirmed by pelvic MRI (meeting any of the following criteria: clinical stage cT3N+ or cT4N0/+; MRF+ or EMVI+; enlarged lateral pelvic lymph nodes).
  • ECOG PS of 0-1.
  • Expected survival ≥2 years.
  • No prior anti-tumor therapy.
  • At least one measurable lesion with a longest diameter ≥10 mm measured by MRI (by RECIST version 1.1).
  • Organ functions meeting the following requirements (no blood products or cell growth factors allowed within 14 days prior to enrollment):

Absolute neutrophil count ≥1.5×10⁹/L; Platelet count ≥100×10⁹/L; Hemoglobin ≥90 g/L; Total bilirubin <1.5×ULN; ALT and/or AST <2.5×ULN; Serum creatinine <1.5×ULN; Creatinine clearance ≥50 mL/min.

  • Women of childbearing potential must use effective contraceptive measures.
  • Good compliance and willingness to comply with follow-up requirements.

Exclusion Criteria:

  • Unable to comply with the study protocol or study procedures.
  • Patients with contraindications to surgery.
  • Patients with metastatic disease or recurrent rectal cancer.
  • Uncontrolled active autoimmune disease or active inflammatory disease at enrollment, or receiving immunosuppressive therapy.
  • History of organ transplantation.
  • Known interstitial lung disease (ILD) or unexplained persistent cough and dyspnea.
  • Patients with familial adenomatous polyposis (FAP), hereditary non-polyposis colorectal cancer (HNPCC), active Crohn's disease, or active ulcerative colitis.
  • Other malignancy diagnosed within 5 years prior to enrollment, except for radically resected basal cell or squamous cell carcinoma of the skin, or carcinoma in situ of the cervix.
  • Severe cardiovascular disease within 6 months prior to enrollment, including unstable angina pectoris or myocardial infarction.
  • Subjects with hypersensitivity to the investigational product or any of its excipients.
  • Participation in another clinical trial of an unapproved/investigational drug within 4 weeks prior to enrollment and having received the corresponding investigational product.
  • Clinically significant electrolyte abnormalities judged by the investigator.
  • Uncontrolled hypertension prior to enrollment, defined as systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg despite medication.
  • Poorly controlled diabetes mellitus prior to enrollment (fasting glucose concentration ≥ CTCAE Grade 2 after standard treatment).
  • Any disease or condition affecting drug absorption prior to enrollment, or inability of the patient to take oral medication.
  • Active gastrointestinal diseases such as gastric and duodenal ulcer, ulcerative colitis prior to enrollment, or other conditions judged by the investigator that may cause gastrointestinal bleeding or perforation.
  • Severe active bleeding within 3 months prior to enrollment, hemoptysis (>5 mL fresh blood within 4 weeks), or thromboembolic event (including stroke and/or transient ischemic attack) within 12 months.
  • Clinically significant cardiovascular disease including but not limited to: acute myocardial infarction, severe/unstable angina pectoris, or coronary artery bypass grafting within 6 months prior to enrollment; congestive heart failure with New York Heart Association (NYHA) classification > Grade 2; ventricular arrhythmia requiring pharmacotherapy; left ventricular ejection fraction (LVEF) < 50%.
  • Active or uncontrolled severe infection (≥ CTCAE v5.0 Grade 2).
  • Known human immunodeficiency virus (HIV) infection. Known clinically significant liver disease history, including viral hepatitis:
  • Hepatitis B virus (HBV) carriers with active HBV infection (HBV DNA positive: >1×10⁴ copies/mL or >2000 IU/mL);
  • Known hepatitis C virus (HCV) infection with positive HCV RNA (>1×10³ copies/mL).
  • Unresolved toxicities higher than CTCAE v5.0 Grade 1 resulting from any prior anti-cancer therapy, excluding alopecia, lymphopenia, and oxaliplatin-induced neurotoxicity ≤ Grade 2.
  • Female subjects who are pregnant (positive pregnancy test before treatment) or breastfeeding.
  • Urinalysis showing urine protein ≥ 2+ and 24-hour urinary protein > 1.0 g.
  • Any other disease, clinically significant metabolic abnormality, physical examination abnormality, or laboratory abnormality that, in the investigator's judgment, renders the patient unsuitable for the study drug (e.g., seizure disorder requiring treatment), interferes with the interpretation of study results, or places the patient at high risk.
  • Patients considered unsuitable for inclusion in this study by the investigator.

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: SCRT+Sintilimab+Cetuximab N01/Bevacizumab+mFOLFOX6/CAPOX

SCRT: 25 Gy, 5 Gy × 5 fr.

One week after completion of SCRT:

  1. Patients with wild-type RAS/BRAF:

    mFOLFOX6: oxaliplatin 85 mg/m², leucovorin 400 mg/m², 5-fluorouracil 400 mg/m² IV bolus on Day 1; followed by 5-fluorouracil 2400 mg/m² continuous infusion over 46 hours, q2w; sintilimab 200 mg/m² IV infusion on Day 1, q3w; cetuximab N01 500 mg/m² IV infusion on Day 1, q2w; Combination therapy for 18 weeks (9 cycles of chemotherapy).

  2. Patients with mutant RAS/BRAF:

CAPOX: oxaliplatin 130 mg/m² IV ivgtt, D1; capecitabine 1000 mg/m² BID, po, D1-14, q3w, for 6 cycles; sintilimab 200 mg/m² ivgtt, D1, q3w, for 6 cycles; bevacizumab 7.5 mg/kg IV infusion on Day 1, q3w, for 5 cycles

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Complete Response (CR)
Periodo de tiempo: Within 3 months after surgery
CR = Pathological Complete Response (pCR) + Clinical Complete Response (cCR)
Within 3 months after surgery

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
R0 resection rate
Periodo de tiempo: Within 3 months after surgery
Proportion of patients achieving a margin-negative tumor removal
Within 3 months after surgery
LER
Periodo de tiempo: Within 3 months after surgery
Local Excision rate
Within 3 months after surgery
ORR
Periodo de tiempo: Around 6 months after recruitment
Objective Response Rate of neoadjuvant therapy ( by RECIST 1.1)
Around 6 months after recruitment
DCR
Periodo de tiempo: Around 6 months after recruitment
Disease Control Rate of neoadjuvant therapy (by RECIST 1.1)
Around 6 months after recruitment
3y-EFS
Periodo de tiempo: Around 3 years after recruitment
3 years events-free survival
Around 3 years after recruitment
3y-RFS
Periodo de tiempo: Around 3 years after recruitment
3 years recurrence-free Survival
Around 3 years after recruitment
OS
Periodo de tiempo: Around 5 years after recruitment
Overall Survival
Around 5 years after recruitment
Safety Measures
Periodo de tiempo: Within 3 months after surgery
Incidence and grades of treatment related adverse events (by NCI-CTCAE 5.0) and surgery related safeties
Within 3 months after surgery

Colaboradores e Investigadores

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

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 (Estimado)

1 de mayo de 2026

Finalización primaria (Estimado)

1 de abril de 2027

Finalización del estudio (Estimado)

1 de abril de 2028

Fechas de registro del estudio

Enviado por primera vez

21 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

5 de mayo de 2026

Publicado por primera vez (Actual)

12 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de mayo de 2026

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

14 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • KL-A140-02

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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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