Chemo-immunotherapy for Cervical Cancer Stage IIICp Trial

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorWomen's Hospital School Of Medicine Zhejiang University

About this trial

Efficacy evaluation of camrelizumab combined with chemotherapy for adjuvant treatment of patients with pathologically confirmed lymph node-positive cervical cancer after staging surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with cervical cancer staged FIGO2018 IIIC1p or IIIC2p after radical surgery;

Positive PD-L1 expression;

ECOG score ≤1

Disqualifiers

Positive parametrium or surgical margin;

Incomplete radical surgery;

Residual target lesions;

Active autoimmune disease or autoimmune disease requiring systemic treatment;

Trial design

Design model

Single group

Treatments tested in this trial

  • Camrelizumab combined with chemotherapy

    Drug

    Camrelizumab combined with chemotherapy for adjuvant treatment of patients with pathologically confirmed lymph node-positive cervical cancer after staging surgery

Treatment groups

59 Participants
are divided into 1 treatment group
Group A: chemotherapy groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

3-year disease-free survival rate

Time frame
from enrollment until the date of first documented recurrence or date of death from any cause, whichever came first, assessed up to 100 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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