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

28. Juni 2026 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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

Studientyp

Interventionell

Einschreibung (Geschätzt)

50

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

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

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Pathological Complete Response (pCR) Rate
Zeitfenster: 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.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Major Pathological Response(MPR) Rate
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

10. Juli 2026

Primärer Abschluss (Geschätzt)

31. Januar 2028

Studienabschluss (Geschätzt)

30. Juni 2029

Studienanmeldedaten

Zuerst eingereicht

24. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

28. Juni 2026

Zuerst gepostet (Tatsächlich)

1. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

1. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

28. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

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.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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