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Neoadjuvant Short-Course Radiotherapy Plus Tislelizumab and Chemotherapy for Locally Advanced Resectable Esophageal Squamous Cell Carcinoma

28 de junho de 2026 atualizado por: Tang-Du Hospital

Neoadjuvant Short-Course Radiotherapy Followed by Tislelizumab Combined With Chemotherapy for Locally Advanced Resectable Esophageal Squamous Cell Carcinoma: A Prospective, Multicenter, Exploratory Study

Neoadjuvant Short-Course Radiotherapy Followed by Tislelizumab Plus Chemotherapy for Locally Advanced Resectable Esophageal Squamous Cell Carcinoma This is a prospective, randomized, two-arm, parallel-group, multicenter, exploratory Phase II clinical trial. It aims to evaluate the efficacy and safety of neoadjuvant short-course radiotherapy followed by tislelizumab combined with chemotherapy in participants with locally advanced resectable esophageal squamous cell carcinoma (ESCC).

Eligible participants will be randomized in a 1:1 ratio to receive either low-dose or high-dose short-course radiotherapy, followed by tislelizumab, nab-paclitaxel, and carboplatin for 3 cycles. Surgery will be performed 4-6 weeks after the last neoadjuvant treatment.

Primary endpoint: Pathological Complete Response (pCR) rate. Secondary endpoints: Major Pathological Response (MPR) rate, Objective Response Rate (ORR), R0 resection rate, downstaging rate, 3-year Event-Free Survival (EFS), 3-year Overall Survival (OS), safety profile, and quality of life.

Approximately 50 participants will be enrolled. Randomization will be stratified by tumor location, clinical T stage, and clinical N stage using a stratified block design via an EDC/IWRS system.

Visão geral do estudo

Descrição detalhada

Study Protocol Full Document Official Title Neoadjuvant Short-Course Radiotherapy Followed by Tislelizumab Combined With Chemotherapy for Locally Advanced Resectable Esophageal Squamous Cell Carcinoma: A Prospective, Multicenter, Exploratory Study Acronym SCR-TILES-ESCC Brief Summary This is a prospective, randomized, two-arm, parallel-group, multicenter, exploratory Phase II clinical trial. It aims to evaluate the efficacy and safety of neoadjuvant short-course radiotherapy followed by tislelizumab plus chemotherapy in participants with locally advanced resectable esophageal squamous cell carcinoma (ESCC). Eligible participants will be randomized 1:1 to receive low-dose or high-dose short-course radiotherapy, followed by 3 cycles of tislelizumab, nab-paclitaxel, and carboplatin. Surgery will be performed 4-6 weeks after the last neoadjuvant treatment. The primary endpoint is pathological complete response (pCR) rate. Secondary endpoints include major pathological response (MPR) rate, objective response rate (ORR), R0 resection rate, downstaging rate, 3-year event-free survival (EFS), 3-year overall survival (OS), safety, and quality of life. A total of 50 participants will be enrolled. Randomization will be stratified by tumor location, clinical T stage, and clinical N stage via an EDC/IWRS system using a stratified block design.

Detailed Description This is a prospective, randomized, two-arm, parallel-group, multicenter, exploratory Phase II clinical trial designed to evaluate the efficacy and safety of neoadjuvant short-course radiotherapy followed by tislelizumab combined with chemotherapy in participants with locally advanced resectable esophageal squamous cell carcinoma (ESCC).

  1. Study Rationale Neoadjuvant chemoradiotherapy followed by surgery is the standard of care for locally advanced esophageal cancer. However, recurrence remains high, and treatment-related toxicities may limit clinical application. Immunotherapy combined with chemotherapy has demonstrated promising pathological response rates in the neoadjuvant setting for ESCC. Radiotherapy can induce immunogenic cell death and enhance the anti-tumor effect of immune checkpoint inhibitors. This trial investigates a novel sequential strategy: short-course radiotherapy followed by tislelizumab plus chemotherapy, to optimize efficacy while minimizing perioperative complications.
  2. Study Design

    This is a randomized, controlled, parallel-group Phase II study. Eligible participants will be randomized in a 1:1 ratio to two treatment groups via an electronic data capture (EDC) / interactive web randomization system (IWRS) using stratified block randomization. Stratification factors are:

    Tumor location (upper thoracic esophagus / middle thoracic esophagus / lower thoracic esophagus) Clinical T stage (cT1-2 vs. cT3-4a) Clinical N stage (cN0 vs. cN+) Block size will be randomly set to 4 or 6 to ensure allocation concealment. Total planned enrollment: 50 participants.

  3. Study Population Inclusion Criteria Voluntarily signed written informed consent. Age 18-75 years, inclusive. Expected survival ≥ 3 months. Clinically judged to be resectable with expected R0 resection. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1. Histologically confirmed, treatment-naive, locally advanced resectable non-cervical esophageal squamous cell carcinoma: T1N1-3M0 or T2-4aN0-3M0 (T2 ≥3 cm or poorly differentiated).

    No suspicious metastatic cervical lymph nodes on neck ultrasound or enhanced CT; no distant metastasis on imaging.

    Presence of measurable tumor lesions. Adequate organ function confirmed by screening laboratory tests. Fertile males and females of childbearing potential agree to use effective contraception during study treatment and for 6 months after the last dose.

    Good compliance with study follow-up. Exclusion Criteria Previous treatment with PD-1/PD-L1 inhibitors or other T-cell targeted agents. Active or suspected autoimmune disease. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage.

    History of ≥ Grade 2 interstitial lung disease. Systemic corticosteroids (>10 mg/day prednisone equivalent) or other immunosuppressants within 14 days before first study treatment.

    Immunodeficiency disease, organ transplantation, or allogeneic hematopoietic stem cell transplantation.

    Live vaccine within 4 weeks before first study treatment. Severe cardiovascular or cerebrovascular disease. Uncontrolled severe comorbidities or active infection requiring systemic antibiotics.

    HIV positive; active hepatitis B or hepatitis C infection. Active tuberculosis. Other active malignancy within the past 2 years. History of drug abuse or psychiatric disorder. Pregnant or lactating female. Any other condition that may increase study risk or interfere with result interpretation (investigator's judgment).

  4. Treatment Interventions Group A: Low-dose radiotherapy group Radiotherapy: 10 Gy in 5 fractions (2.0 Gy per fraction)

    Two days after radiotherapy:

    Tislelizumab 200 mg IV Day 1 Q3W Nab-paclitaxel 125 mg/m² IV Day 1, Day 8 Q3W Carboplatin AUC=5 IV Day 1 Q3W 3 cycles total Group B: High-dose radiotherapy group Radiotherapy: 15 Gy in 5 fractions (3.0 Gy per fraction)

    Two days after radiotherapy:

    Tislelizumab, nab-paclitaxel, carboplatin same as Group A 3 cycles total Surgery Surgery will be performed 4-6 weeks after completion of the third neoadjuvant cycle. Surgical approaches include McKeown esophagectomy, Ivor-Lewis esophagectomy, open, thoracoscopic, or robotic-assisted surgery. All procedures will aim for R0 resection.

  5. Randomization This study will use a 1:1 randomized, stratified, block randomization design implemented via the EDC/IWRS system. Randomization will be stratified by tumor location, clinical T stage, and clinical N stage. A random block size (4 or 6) will be applied within each stratum to ensure balanced group allocation and effective allocation concealment. The randomization sequence will be generated by an independent statistician and securely stored in the EDC/IWRS system. Investigators, patients, and outcome assessors will be unaware of the block size and randomization list to avoid selection bias.
  6. Study Assessments Tumor Evaluation Baseline, pre-Cycle 3, pre-surgery: enhanced chest CT/MRI Response evaluated by RECIST v1.1 Postoperative pathology: tumor regression, residual disease, lymph nodes, margin status, pTNM stage Safety Assessments Adverse events (AEs) graded by CTCAE v5.0 Monitoring of AEs, SAEs, and immune-related AEs (irAEs) Laboratory tests, ECG, echocardiography, physical exams at each visit Quality of Life Assessed by SF-36 questionnaire
  7. Study Endpoints Primary Endpoint Pathological Complete Response (pCR) rate: no residual viable tumor cells in primary tumor bed and all sampled lymph nodes.

    Secondary Endpoints Major Pathological Response (MPR) rate: residual viable tumor ≤10% Objective Response Rate (ORR): CR + PR per RECIST v1.1 R0 resection rate Downstaging rate 3-year Event-Free Survival (EFS) 3-year Overall Survival (OS) Safety profile Quality of life

  8. Follow-up Plan Safety follow-up: 30 (±7) days after last study treatment Survival follow-up: every 3 months for 2 years, every 6 months up to 5 years, then annually Assessments: physical exam, chest CT, tumor markers, blood biochemistry, survival status
  9. Statistical Methods pCR, MPR, ORR, R0 resection rate, downstaging rate: descriptive statistics (n, %, 95%CI) EFS, OS: Kaplan-Meier method, log-rank test Safety: frequency and severity summary QoL: t-test/ANCOVA (between groups); paired t-test (within groups)
  10. Study Timeline First patient enrollment: Q3 2026 Last patient enrollment: Q1 2028 Study completion: Q2 2029

Tipo de estudo

Intervencional

Inscrição (Estimado)

50

Estágio

  • Fase 2

Contactos e Locais

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Contato de estudo

Locais de estudo

    • Shaanxi
      • Xi'an, Shaanxi, China, 710038
        • Tangdu Hospital, Fourth Military Medical University
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Voluntarily provided written informed consent prior to any study-related procedures
  • Aged 18 to 75 years, male or female
  • Life expectancy of at least 3 months
  • Predicted to achieve R0 surgical resection
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Histologically confirmed, treatment-naive, resectable locally advanced thoracic esophageal squamous cell carcinoma (ESCC) meeting the staging criteria: T1 N1-3 M0 or T2-4a N0-3 M0 (T2 ≥3 cm or poorly differentiated). No suspected metastatic cervical lymph nodes (except for upper thoracic esophageal cancer regional lymph nodes) on neck ultrasound or contrast-enhanced CT, and no distant metastasis on imaging
  • Presence of measurable tumor lesions.
  • Adequate organ function defined by laboratory parameters: Absolute neutrophil count (ANC) ≥1.5×10⁹/L; platelet count ≥100×10⁹/L; hemoglobin ≥90 g/L. Total bilirubin ≤1.5×ULN; AST and ALT ≤2.5×ULN. Serum creatinine ≤1.5×ULN or calculated creatinine clearance ≥60 mL/min. INR ≤1.5, PT and APTT ≤1.5×ULN
  • Men and women of childbearing potential must use effective contraception during treatment and for 6 months after the last dose of study treatment
  • Good compliance and ability to complete scheduled follow-up.

Exclusion Criteria:

  • Prior treatment with PD-1/PD-L1 inhibitors or other immunomodulatory agents targeting T-cell receptors (e.g., CTLA-4, OX40)
  • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage
  • Active or suspected autoimmune disease, including systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, except type 1 diabetes controlled by replacement therapy, hypothyroidism, or skin disorders not requiring systemic therapy
  • History of grade ≥2 interstitial lung disease
  • Systemic corticosteroids (>10 mg prednisone daily or equivalent) or other immunosuppressive agents within 14 days before first study treatment
  • Primary or acquired immunodeficiency, organ transplantation, allogeneic hematopoietic stem cell transplantation
  • Live vaccine within 4 weeks before first study treatment
  • Severe uncontrolled cardiovascular or cerebrovascular disease: Uncontrolled hypertension or pulmonary hypertension. Unstable angina, myocardial infarction, coronary artery bypass grafting, or stent implantation within 6 months. NYHA class ≥2 chronic heart failure. Left ventricular ejection fraction (LVEF) <50%.

Clinically significant arrhythmia requiring treatment. Cerebrovascular accident (CVA) or transient ischemic attack (TIA) within 6 months. Uncontrolled active infection requiring systemic antibiotics. Positive HIV test, active hepatitis B or hepatitis C infection (exceptions: HBV DNA <500 IU/mL; HCV RNA undetectable).

Active pulmonary tuberculosis (TB). Other active malignancy within the previous 2 years, except adequately treated thyroid cancer, carcinoma in situ of the cervix, basal/squamous cell skin cancer, or ductal carcinoma in situ of the breast

  • History of drug abuse or psychiatric disorder
  • Pregnant or lactating women
  • Any other severe medical, psychiatric, or laboratory abnormality that, in the investigator's opinion, would increase study-related risk or interfere with result interpretation.

Plano de estudo

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Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Low-Dose Radiotherapy + Tislelizumab + Chemotherapy
Neoadjuvant low-dose short-course radiotherapy (10 Gy in 5 fractions) followed by tislelizumab combined with nab-paclitaxel and carboplatin for 3 cycles, then surgical resection.
Albumin-bound paclitaxel at a dose of 125 mg/m² is administrated intravenously on day 1 and day 8 of each 3-week cycle, for a total of 3 cycles.
Neoadjuvant short-course radiotherapy with a total dose of 10 Gy, delivered in 5 daily fractions of 2.0 Gy per fraction, administered consecutively before systemic combination therapy.
Anti-PD-1 monoclonal antibody tislelizumab 200 mg is given by intravenous infusion on day 1 of each 3-week cycle, for up to 3 cycles in the neoadjuvant treatment phase.
Carboplatin is given intravenously on day 1 of each cycle at a targeted AUC of 5, repeated every 3 weeks for 3 cycles as part of neoadjuvant combination regimen.
Experimental: High-Dose Radiotherapy + Tislelizumab + Chemotherapy
Neoadjuvant high-dose short-course radiotherapy (15 Gy in 5 fractions) followed by tislelizumab combined with nab-paclitaxel and carboplatin for 3 cycles, then surgical resection.
Albumin-bound paclitaxel at a dose of 125 mg/m² is administrated intravenously on day 1 and day 8 of each 3-week cycle, for a total of 3 cycles.
Anti-PD-1 monoclonal antibody tislelizumab 200 mg is given by intravenous infusion on day 1 of each 3-week cycle, for up to 3 cycles in the neoadjuvant treatment phase.
Carboplatin is given intravenously on day 1 of each cycle at a targeted AUC of 5, repeated every 3 weeks for 3 cycles as part of neoadjuvant combination regimen.
Neoadjuvant short-course radiotherapy with a total dose of 15 Gy, delivered in 5 daily fractions of 3.0 Gy per fraction, administered consecutively before systemic combination therapy.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Pathological Complete Response (pCR) Rate
Prazo: Within 1 week after surgical resection.
The primary outcome measure is the rate of pathological complete response (pCR) after completion of neoadjuvant treatment. Pathological complete response is defined as the absence of residual invasive cancer cells in the primary esophageal tumor bed and all sampled regional lymph nodes, confirmed by postoperative pathological examination by a qualified pathologist.
Within 1 week after surgical resection.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Major Pathological Response(MPR) Rate
Prazo: Within 1 week after surgical resection
Major pathological response is defined as the residual tumor burden being ≤10% of the primary tumor bed. This outcome measures the proportion of participants who achieve major pathological response after receiving the study intervention, reflecting the effectiveness of the treatment regimen in reducing tumor burden.
Within 1 week after surgical resection
R0 Resection Rate
Prazo: At the time of surgical resection
R0 resection rate refers to the proportion of participants who achieve complete surgical resection with negative surgical margins (no residual tumor tissue at the resection edges), which is an important indicator of surgical efficacy and long-term prognosis.
At the time of surgical resection
Incidence of Treatment-Related Adverse Events (CTCAE v5.0)
Prazo: From start of neoadjuvant treatment through 30 days after last study treatment
To evaluate the incidence, type and severity of treatment-related adverse events graded according to Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0 in all enrolled participants.
From start of neoadjuvant treatment through 30 days after last study treatment
Objective Response Rate (ORR)
Prazo: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to surgical resection
The proportion of participants achieving complete response (CR) or partial response (PR) evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to surgical resection
3-Year Event-Free Survival (EFS) Rate
Prazo: Followed up for up to 3 years from the date of randomization.
Event-free survival defined as the time from randomization to first occurrence of local recurrence, distant metastasis, tumor progression, or death from any cause, whichever comes first.
Followed up for up to 3 years from the date of randomization.
3-Year Overall Survival (OS) Rate
Prazo: Up to 3 years from randomization
Overall survival defined as the time from randomization to death from any cause; the proportion of participants alive at 3 years after randomization will be reported.
Up to 3 years from randomization
Change in SF-36 Quality of Life Scale Score
Prazo: Baseline prior to neoadjuvant therapy, Perioperative (after all neoadjuvant cycles before surgery), 3 months post-surgery, 6 months post-surgery, 12 months post-surgery
The 36-Item Short Form Health Survey (SF-36). The total score ranges from 0 to 100; higher scores indicate better health-related quality of life. Changes in health-related quality of life measured by the SF-36 questionnaire across physical, mental and social function domains.
Baseline prior to neoadjuvant therapy, Perioperative (after all neoadjuvant cycles before surgery), 3 months post-surgery, 6 months post-surgery, 12 months post-surgery

Colaboradores e Investigadores

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Patrocinador

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

10 de julho de 2026

Conclusão Primária (Estimado)

31 de janeiro de 2028

Conclusão do estudo (Estimado)

30 de junho de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

24 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

28 de junho de 2026

Primeira postagem (Real)

1 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

1 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

De-identified individual participant data (IPD) will not be made available to other researchers. This is an investigator-initiated exploratory trial with no formal data sharing platform or repository established.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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