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Toripalimab With Chemoradiotherapy for Locally Advanced Cervical Cancer

Tests adding toripalimab to chemoradiotherapy in adults with locally advanced cervical cancer.

Plain-language title generated from the registry record
Registry title: Toripalimab Combined With Definitive CCRT for LACC Patients

Key facts

Where
Shanghai, ChinaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for women with newly diagnosed, untreated locally advanced squamous cell cancer of the cervix. It tests toripalimab added to chemoradiotherapy against chemoradiotherapy alone.

Age
More than 18 years old
Sex
Women only
Disease stage
Locally advanced squamous cell carcinoma of the cervix, FIGO 2018 stage IB3 to IVA, with no sign of distant spread
Earlier treatment
No earlier treatment for this cancer. No earlier or current PD-1 antibody treatment or other immunotherapy aimed at PD-1/PD-L1.

Main reasons for not taking part

  • Previous immunodeficiency disorders
  • Any condition the researchers think raises the risk of treatment
  • Earlier or current PD-1 antibody or other PD-1/PD-L1 immunotherapy
  • Major organ failure

Read by machine on 9 November 2026.

Where in China

  • Ruijin hospitalShanghai, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Ruijin Hospital
Trial code
NCT06256224
Record updated
24 April 2024
Original description
Cervical cancer constitutes a significant health burden for women globally. While most patients with early-stage disease can be cured with radical surgery or chemoradiotherapy, patients with high-risk locally advanced disease or with recurrent/metastatic disease have a poor prognosis with standard treatments. Immunotherapies are a rational treatment for this HPV-driven cancer that commonly expresses programmed cell death ligand-1. Toripalimab, a humanized immunoglobulin G4 monoclonal antibody against PD-1, showed promising anti-tumor efficacy in multiple solid tumors. This randomised study is evaluating toripalimab combined with CCRT versus CCRT alone for treatment-naïve LACC.Read full original descriptionShow less

Toripalimab Combined With Definitive Chemoradiotherapy for Locally Advanced Cervical Squamous Cell Carcinoma Patients

Cervical cancer constitutes a significant health burden for women globally. While most patients with early-stage disease can be cured with radical surgery or chemoradiotherapy, patients with high-risk locally advanced disease or with recurrent/metastatic disease have a poor prognosis with standard treatments. Immunotherapies are a rational treatment for this HPV-driven cancer that commonly expresses programmed cell death ligand-1. Toripalimab, a humanized immunoglobulin G4 monoclonal antibody against PD-1, showed promising anti-tumor efficacy in multiple solid tumors. This randomised study is evaluating toripalimab combined with CCRT versus CCRT alone for treatment-naïve LACC.

Inclusion: more than 18 years old females; had newly diagnosed and previously untreated locally advanced squamous cell carcinoma of the uterine cervix; FIGO 2018 stage IB3 to IVA with no evidence of distant metastasis; ECOG PS 0-1 without major organ failure; signed informed consent voluntarily.

Exclusion: previously suffered from immunodeficiency disorders; Previously received or currently receiving other PD-1 antibody treatments or other immunotherapies targeting PD-1/PD-L1; had any condition that researchers believed to be associated with increased risk of treatment.

ClinicalTrials.gov NCT06256224