Biomarker Based Neoadjuvant Strategies for Locally Advanced Resectable ESCC

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorFujian Medical University Union Hospital

About this trial

This study aims to evaluate the impact of the neoadjuvant treatment strategy based on CPS score on the pathological complete response (pCR) rate in patients with resectable locally advanced esophageal cancer.

Eligibility criteria

Qualifiers

Diagnosis: Histologically confirmed esophageal squamous cell carcinoma (ESCC).

Stage: Resectable locally advanced ESCC (clinical stage II-III according to the AJCC/UICC 8th edition).

Age: 18-75 years old.

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

Disqualifiers

Distant Metastasis: Presence of distant metastasis.

Other Malignancies: History of other malignancies within the past 5 years, except for adequately treated carcinoma in situ of the cervix, basal or squamous cell skin carcinoma, or other localized non-invasive malignancy.

Autoimmune Diseases: History of active autoimmune diseases requiring systemic treatment within the past 2 years.

Infections: Active infection requiring systemic therapy.

Trial design

Treatments tested in this trial

  • Serplulimab
  • Paclitaxel+Cisplatin (Neoadjuvant Chemotherapy)
  • Paclitaxel+Cisplatin(Concurrent Chemoradiotherapy)
  • Radiotherapy

Treatment groups

90 Participants
are divided into 3 treatment groups