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Early Response-guided Sequential Radiotherapy After Chemoimmunotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma (Keystone006)

Early Response-guided Sequential Radiotherapy After Chemoimmunotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma: A Phase II Clinical Study

Esophageal squamous cell carcinoma (ESCC) is a common and aggressive malignancy with poor prognosis, particularly in patients with locally advanced disease. Neoadjuvant chemoimmunotherapy has shown promising antitumor activity and may improve pathological response; however, a proportion of patients achieve only stable disease (SD) or progressive disease (PD) after initial treatment and may have limited benefit from proceeding directly to surgery.

This prospective, single-center, phase II clinical study aims to evaluate an early response-guided sequential selective radiotherapy strategy after neoadjuvant chemoimmunotherapy in patients with locally advanced, resectable ESCC. Patients will initially receive neoadjuvant chemotherapy combined with PD-1 inhibitor therapy. Based on radiological response assessment, patients with major response (complete response or partial response) will proceed directly to radical surgery, whereas patients with insufficient response (stable disease or progressive disease but still considered resectable) will receive sequential chemoradiotherapy followed by surgery.

The study aims to assess the safety and efficacy of this individualized treatment strategy, with primary evaluation focusing on pathological response, surgical outcomes, and treatment-related adverse events. Exploratory analyses will investigate potential biomarkers associated with treatment response and prognosis.

Studieoversikt

Detaljert beskrivelse

Esophageal squamous cell carcinoma (ESCC) is a major subtype of esophageal cancer and remains associated with poor outcomes, particularly in patients with locally advanced disease. Neoadjuvant chemoimmunotherapy has recently emerged as a promising treatment approach for resectable ESCC, improving tumor response and pathological remission. However, a subset of patients demonstrates limited response after initial therapy, and optimal management strategies for these patients remain uncertain.

Radiotherapy may enhance antitumor immune responses through modulation of the tumor microenvironment and may provide additional tumor control in patients with insufficient response to initial systemic therapy. Therefore, an individualized treatment strategy guided by early treatment response may help optimize therapeutic benefit while preserving opportunities for curative surgery.

This study evaluates an early response-guided sequential selective radiotherapy strategy for patients with locally advanced resectable ESCC after neoadjuvant chemoimmunotherapy. Treatment decisions will be adapted according to early tumor response assessment and multidisciplinary evaluation, aiming to provide additional local treatment for patients with inadequate response while avoiding unnecessary radiotherapy in patients with favorable response.

The study will assess the safety, feasibility, and clinical outcomes of this response-guided approach. In addition, exploratory analyses will investigate potential biomarkers associated with treatment response and prognosis, including changes in the tumor immune microenvironment and peripheral blood biomarkers.

This study aims to develop a personalized treatment strategy for locally advanced ESCC based on early therapeutic response and to improve clinical outcomes through optimized treatment selection.

Studietype

Intervensjonell

Registrering (Antatt)

110

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

      • Tianjin, Kina, 300060
        • Department of minimally invasive esophageal surgery, Tianjin Medical University Cancer Institute and Hospital
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

-

Participants must meet all of the following criteria:

Provide written informed consent before enrollment.

Age >18 years, male or female.

Histologically confirmed thoracic esophageal squamous cell carcinoma (ESCC).

Locally advanced, resectable disease according to AJCC/UICC 8th edition TNM staging system, defined as:

cT3-4aN0-2M0 or cT1-2N1-2M0;

No evidence of distant metastasis;

Considered initially resectable by a multidisciplinary surgical team.

Patients who have received neoadjuvant chemoimmunotherapy and have measurable disease response assessment according to RECIST v1.1, including complete response (CR), partial response (PR), stable disease (SD), or progressive disease (PD).

At least one measurable lesion according to RECIST version 1.1.

Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

Expected survival time >6 months.

Adequate organ function meeting the following criteria:

Bone marrow function:

Absolute neutrophil count ≥1,500/mm³;

Platelet count ≥100,000/mm³;

Hemoglobin ≥9 g/dL.

Renal function:

Serum creatinine ≤1.5 mg/dL and/or creatinine clearance ≥60 mL/min.

Hepatic function:

Total bilirubin ≤1.5 × upper limit of normal (ULN);

AST and ALT ≤1.5 × ULN.

Participants of childbearing potential must agree to use medically approved contraception during study treatment and for 3 months after completion of treatment. Female participants of childbearing potential must have a negative serum or urine pregnancy test within 7 days before enrollment and must not be breastfeeding.

Willingness and ability to comply with study procedures, safety assessments, and survival follow-up.

Exclusion Criteria:

-

Participants will be excluded if any of the following criteria apply:

Evidence of distant metastasis.

Previous or concurrent malignancy, except adequately treated basal cell carcinoma of skin or cervical carcinoma in situ.

Previous thoracic radiotherapy.

Previous treatment with PD-1, PD-L1, or CTLA-4 inhibitors, or known hypersensitivity to PD-1 inhibitors or macromolecular protein products.

Active autoimmune disease or history of clinically significant autoimmune disease requiring systemic treatment.

Current use of immunosuppressive therapy or systemic corticosteroids exceeding the equivalent of prednisone 10 mg/day within 2 weeks before enrollment.

Clinically significant ascites or pleural effusion requiring therapeutic drainage.

Uncontrolled cardiovascular disease, including:

NYHA class II or higher heart failure;

Unstable angina;

Myocardial infarction within 1 year;

Clinically significant arrhythmias requiring treatment.

Significant coagulation abnormalities, bleeding tendency, or ongoing thrombolytic/anticoagulant therapy.

Active gastrointestinal disorders associated with bleeding or perforation risk, including esophageal varices, active gastric/duodenal ulcer, ulcerative colitis, portal hypertension, or active tumor bleeding.

History of severe bleeding, clinically significant hemoptysis, or thromboembolic events within specified periods.

Active infection or unexplained fever >38.5°C before treatment initiation.

Abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 4 weeks before study treatment.

History or evidence of interstitial lung disease, pulmonary fibrosis, radiation pneumonitis, drug-induced pneumonitis, pneumoconiosis, or severe pulmonary impairment.

Known immunodeficiency, including HIV infection, or active hepatitis infection requiring exclusion according to protocol criteria.

Participation in another clinical trial within 1 month before enrollment or concurrent systemic anticancer therapy.

Receipt of live vaccines within 4 weeks before treatment or planned live vaccination during study treatment.

Known history of substance abuse, alcoholism, or drug abuse.

Inability or unwillingness to comply with study-related procedures, examinations, or required costs.

Any other medical, psychological, social, or safety-related condition judged by the investigator to make the participant unsuitable for study participation.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Response-guided Sequential Treatment
Participants will receive neoadjuvant chemoimmunotherapy followed by individualized treatment according to early tumor response assessment. Patients with favorable response will proceed to surgery, while patients with insufficient response but remaining resectable disease will receive sequential chemoradiotherapy followed by surgery.

Participants will receive neoadjuvant chemoimmunotherapy before surgery.

The regimen includes:

Tislelizumab (PD-1 inhibitor): 200 mg administered intravenously once every 3 weeks for 2 cycles.

Paclitaxel: 135 mg/m² administered intravenously on Day 1 of each 3-week cycle for 2 cycles.

Cisplatin: 60 mg/m² administered intravenously on Day 1 of each 3-week cycle for 2 cycles.

After completion of neoadjuvant chemoimmunotherapy, tumor response will be assessed. Treatment decisions will be guided by early response evaluation and multidisciplinary surgical assessment.

Participants with inadequate response after neoadjuvant chemoimmunotherapy but remaining eligible for curative surgery will receive sequential chemoradiotherapy followed by surgery.

Concurrent chemoradiotherapy consists of:

Radiotherapy: 1.8 Gy per fraction, 5 fractions per week, for 5 weeks, with a total dose of 41.4 Gy in 23 fractions.

Chemotherapy: weekly concurrent chemotherapy with paclitaxel and platinum-based chemotherapy during radiotherapy.

The treatment aims to improve local tumor control before radical surgical resection.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Safety and Tolerability Equivalent Major Pathological Response Rate (ITT-MPR)
Tidsramme: Up to approximately 1.5 years
Up to approximately 1.5 years

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
R0 Resection Rate
Tidsramme: At the time of surgery after completion of neoadjuvant treatment
The proportion of participants achieving microscopically complete tumor resection (R0 resection) after surgery.
At the time of surgery after completion of neoadjuvant treatment
Surgical Completion Rate
Tidsramme: At the time of surgery after completion of neoadjuvant treatment
The proportion of participants who successfully complete planned surgical resection after neoadjuvant treatment.
At the time of surgery after completion of neoadjuvant treatment
Pathological Complete Response (pCR) Rate
Tidsramme: At the time of 1 month after resection
The proportion of participants achieving pathological complete response (ypT0N0) based on surgical pathology evaluation after neoadjuvant treatment.
At the time of 1 month after resection
Tumor Regression Grade (TRG)
Tidsramme: At the time of surgery after completion of neoadjuvant treatment
Tumor regression grade assessed by pathological examination after surgical resection.
At the time of surgery after completion of neoadjuvant treatment
Pathological Lymph Node Status (ypN0 Rate)
Tidsramme: At the time of surgery after completion of neoadjuvant treatment
The proportion of participants without residual metastatic lymph nodes (ypN0) based on postoperative pathological evaluation.
At the time of surgery after completion of neoadjuvant treatment
Tumor Downstaging Rate
Tidsramme: At the time of surgery after completion of neoadjuvant treatment
The proportion of participants achieving pathological downstaging compared with baseline clinical staging after neoadjuvant treatment.
At the time of surgery after completion of neoadjuvant treatment
Objective Response Rate (ORR)
Tidsramme: After completion of neoadjuvant treatment before surgery (approximately 12 weeks after initiation of study treatment)
The proportion of participants achieving complete response or partial response according to RECIST 1.1 criteria.
After completion of neoadjuvant treatment before surgery (approximately 12 weeks after initiation of study treatment)
Disease Control Rate (DCR)
Tidsramme: After completion of neoadjuvant treatment before surgery
The proportion of participants achieving complete response, partial response, or stable disease according to RECIST 1.1 criteria.
After completion of neoadjuvant treatment before surgery
Treatment-related Adverse Events
Tidsramme: From initiation of study treatment until 30 days after completion of treatment
The incidence and severity of treatment-related adverse events assessed according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
From initiation of study treatment until 30 days after completion of treatment
Perioperative Complications
Tidsramme: Within 30 days after surgery
The incidence of postoperative complications occurring after surgical resection.
Within 30 days after surgery

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Event-Free Survival (EFS)
Tidsramme: Up to 12 months after initiation of study treatment
Event-free survival is defined as the time from initiation of study treatment to disease progression, recurrence, death, or other predefined events.
Up to 12 months after initiation of study treatment
Overall Survival (OS)
Tidsramme: Up to 12 months after initiation of study treatment
Overall survival is defined as the time from initiation of study treatment to death from any cause.
Up to 12 months after initiation of study treatment
Disease-Free Survival (DFS)
Tidsramme: Up to 12 months after surgery
Disease-free survival is defined as the time from R0 surgical resection to disease recurrence or death from any cause.
Up to 12 months after surgery
Quality of Life Assessed by EORTC QLQ-C30
Tidsramme: Baseline and up to 12 months after initiation of study treatment
Quality of life will be assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30).
Baseline and up to 12 months after initiation of study treatment

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

14. juli 2026

Primær fullføring (Antatt)

31. desember 2027

Studiet fullført (Antatt)

31. desember 2031

Datoer for studieregistrering

Først innsendt

13. juli 2026

Først innsendt som oppfylte QC-kriteriene

19. juli 2026

Først lagt ut (Faktiske)

22. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

22. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

19. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

IPD will be shared based on the request from other researchers.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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