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NCT Number: NCT07799077

Paclitaxel Polymeric Micelles and Cisplatin Plus Sintilimab as Neoadjuvant Therapy for Resectable Locally Advanced Esophageal Squamous Cell Carcinoma

Locally advanced Esophageal Squamous Cell Carcinoma (ESCC) has poor prognosis with standard therapies. Neoadjuvant immunochemotherapy improves pathological response rates, but optimal regimens remain undefined. Paclitaxel polymeric micelles offer enhanced tumor targeting (EPR effect) and reduced toxicity vs. conventional paclitaxel formulations, with no need for premedication. This single-arm, prospective trial evaluates the efficacy and safety of neoadjuvant sintilimab combined with paclitaxel polymeric micelles and cisplatin in resectable locally advanced ESCC.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written informed consent was signed before the implementation of any test-related procedures ;
  • Age 18-75 years ;
  • Esophageal squamous cell carcinoma confirmed by histopathology ;
  • Resectable thoracic cT1b-2N1-3M0 or cT2-3N0M0 ;
  • No anti-tumor treatment has been received ;
  • ECOG PS 0-1 ;
  • Expected survival ≥ 3 months ;
  • At least one measurable lesion per RECIST v1.1;
  • Adequate organ function (hematology, liver, kidney, coagulation, thyroid, myocardial enzymes) ;
  • For women of childbearing age, a negative urine or serum pregnancy test should be performed within three days prior to the first study drug administration ( day 1 of the first cycle ). If the urine pregnancy test results cannot be confirmed as negative, a blood pregnancy test is required. Women of non-fertility age were defined as at least 1 year after menopause, or had undergone surgical sterilization or hysterectomy ;
  • If there is a risk of conception, all subjects ( male or female ) are required to use contraception with an annual failure rate of less than 1 % throughout the treatment period up to 120 days after the last study drug administration ( or 180 days after the last study drug administration ).

Exclusion criteria

  • High risk of tracheoesophageal fistula or aortoesophageal fistula
  • Prior radiotherapy, chemotherapy, targeted therapy, or immunotherapy
  • Participation in another interventional clinical trial within 4 weeks before the first dose
  • History of other active malignancies (except cured low-risk tumors, adequately treated non-melanoma skin cancer, or carcinoma in situ)
  • Active uncontrolled hepatitis B/C infection
  • Uncontrolled systemic diseases (e.g., heart failure NYHA ≥II, interstitial lung disease, active autoimmune diseases requiring systemic immunosuppression)
  • Allergy to study drugs or excipients
  • Uncontrolled third-space effusion (e.g., pleural/pericardial effusion)
  • Pregnant or lactating women

Treatment and study plan

Paclitaxel polymer micelles for injection and cisplatin combined with sintilimab

Drug
  • Sindilimab : 200 mg, Q3W, intravenous infusion, D1 ;
  • Paclitaxel polymeric micelles : 300 mg/m2 ; q3W, intravenous infusion, D1 ;
  • Cisplatin : 75 mg/m2 ; q3W ; intravenous infusion, D1 ;

Primary outcomes

  1. Pathological Complete Response (pCR) rate

    Time frame: Assessed via surgical pathology (4-6 weeks post-neoadjuvant therapy)

    Pathological Complete Response (pCR) rate: Proportion of patients with no residual invasive tumor in primary tumor bed and sampled lymph nodes (ypT0/Tis ypN0) after neoadjuvant therapy

Secondary outcomes

  1. Major Pathological Response (MPR) rate

    Time frame: Perioperative

  2. R0 resection rate

    Time frame: Perioperative

  3. Objective Response Rate (ORR) per RECIST v1.1

    Time frame: Assessed at baseline and pre-surgery

  4. Event-Free Survival (EFS)

    Time frame: Follow-up every 3 months for 2 years, then every 6 months up to 5 years

  5. Overall Survival (OS)

    Time frame: Follow-up every 3 months for 2 years, then every 6 months up to 5 years

  6. Safety: Incidence of adverse events (AEs), serious AEs (SAEs), and immune-related AEs (irAEs)

    Time frame: From initiation of treatment to 30 days post-last dose (or 90 days for SAEs)

Study contacts

Contact information is provided by the study sponsor or research team.

Ziqiang Tian

CONTACT

[email protected]

+8618538881000

Sponsors and collaborators

Lead sponsor

Hebei Medical University Fourth Hospital

Other

Collaborators

  • Shanghai Yizhong Pharmaceutical Co., Ltd.

Registry information

Official study title

Paclitaxel Polymeric Micelles and Cisplatin Plus Sintilimab as Neoadjuvant Therapy for Resectable Locally Advanced Esophageal Squamous Cell Carcinoma: A Single-arm, Multicenter, Prospective Phase II Clinical Trial

Important dates

Study start
2026
Primary completion
2027
Study completion
2029
First posted
Sep 2, 2026
Registry last updated
Sep 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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