Tislelizumab Combined With Concurrent Chemoradiotherapy as First-line Treatment for Stage IIIC2 Cervical Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorFirst Affiliated Hospital of Guangxi Medical University

About this trial

To evaluate the efficacy and safety of tislelizumab combined with concurrent chemoradiotherapy in first-line treatment of stage IIIC2 cervical cancer.

Eligibility criteria

Qualifiers

None

Disqualifiers

Diagnosed with any other cancer within the past 5 years;

Known allergy to any component of the drug;

Congenital or acquired immune deficiency (such as HIV infection);

The presence of any active, known or suspected autoimmune disease (such as, but not limited to, interstitial pneumonia, uveitis, enteritis, hepatitis, arthritis, nephritis, hypophysitis, hyperthyroidism, hypothyroidism, etc.); Medical history of vitiligo; asthma which requires bronchodilators for medical intervention;

Trial design

Treatments tested in this trial

  • tislelizumab
  • concurrent chemoradiotherapy

Treatment groups

112 Participants
are divided into 2 treatment groups