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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 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

60

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Guanghai Dai, MD
  • Numero di telefono: +86 13801232381
  • Email: 463043539@qq.com

Luoghi di studio

      • Beijing, Cina
        • China PLAGH

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Complete Response (CR)
Lasso di tempo: Within 3 months after surgery
CR = Pathological Complete Response (pCR) + Clinical Complete Response (cCR)
Within 3 months after surgery

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
R0 resection rate
Lasso di tempo: Within 3 months after surgery
Proportion of patients achieving a margin-negative tumor removal
Within 3 months after surgery
LER
Lasso di tempo: Within 3 months after surgery
Local Excision rate
Within 3 months after surgery
ORR
Lasso di tempo: Around 6 months after recruitment
Objective Response Rate of neoadjuvant therapy ( by RECIST 1.1)
Around 6 months after recruitment
DCR
Lasso di tempo: Around 6 months after recruitment
Disease Control Rate of neoadjuvant therapy (by RECIST 1.1)
Around 6 months after recruitment
3y-EFS
Lasso di tempo: Around 3 years after recruitment
3 years events-free survival
Around 3 years after recruitment
3y-RFS
Lasso di tempo: Around 3 years after recruitment
3 years recurrence-free Survival
Around 3 years after recruitment
OS
Lasso di tempo: Around 5 years after recruitment
Overall Survival
Around 5 years after recruitment
Safety Measures
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 maggio 2026

Completamento primario (Stimato)

1 aprile 2027

Completamento dello studio (Stimato)

1 aprile 2028

Date di iscrizione allo studio

Primo inviato

21 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

5 maggio 2026

Primo Inserito (Effettivo)

12 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • KL-A140-02

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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