Induction Immunotherapy Combined With Chemotherapy Followed by Concurrent Chemoradiotherap and Immunotherapy for Cervical Cancer

NCT ID: NCT07092696

Last Updated: 2025-07-30

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-12-01
• Study Completion Date: 2028-12-01

Brief Summary

To explore the efficacy and tolerability of a platinum-based regimen combined with the PD-1 antibody toripalimab administered prior to concurrent chemoradiotherapy in patients with locally advanced cervical cancer.

Detailed Description

At the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting, investigators reported that neoadjuvant camrelizumab combined with induction chemotherapy, followed by camrelizumab plus concurrent chemoradiotherapy and subsequent camrelizumab maintenance, achieved an overall response rate of 100 % in patients with locally advanced cervical cancer, with an acceptable safety profile.

Pre-clinical studies have suggested that concurrent chemoradiotherapy may dampen immune activation in cervical cancer, including reductions in the CD4+/CD8+ T-cell ratio and decreased T-cell receptor (TCR) diversity. These findings imply that administration of immunotherapy prior to chemoradiotherapy might be more effective than giving it concomitantly or afterwards.

Informed by these clinical and translational data, we propose to conduct an initial, prospective phase II trial to evaluate the efficacy and safety of neoadjuvant chemo-immunotherapy followed by concurrent chemoradiotherapy plus immunotherapy in patients with locally advanced cervical cancer, thereby laying the groundwork for a subsequent phase III investigation.

Conditions

Cervical Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

PD-1 arm

Induction PD-1 inhibitor followed by PD-1 maintenance administered concurrently with chemoradiotherapy and continued after completion.

Group Type: EXPERIMENTAL

Toripalimab

Intervention Type: DRUG

Induction chemo-immunotherapy (platinum-based tri-weekly regimen)

• Paclitaxel 175 mg/m² IV on day 1
• Cisplatin 50 mg/m² IV on day 1 or carboplatin AUC 4-5 IV on day 1
• Toripalimab 240 mg IV on day 1, administered immediately before each chemotherapy infusion Cycle length: every 3 weeks Number of cycles: 2 Concurrent chemoradiotherapy (weekly regimen)
• Radiation therapy delivered according to institutional protocol
• Cisplatin 40 mg/m² IV once weekly
• Toripalimab 240 mg IV on day 1 of every 3-week cycle, given before chemotherapy Cycle length: every 3 weeks during radiotherapy

Maintenance immunotherapy

• Toripalimab 240 mg IV on day 1 every 3 weeks (Q3W) Duration: 1 year (total 13 cycles)

Pelvic External-Beam Radiotherapy (EBRT)

Intervention Type: RADIATION

• PTV: 6 MV photons, 1.80 Gy per fraction × 28 fractions = 50.4 Gy.
• PGTVnd: 6 MV photons, 2.14 Gy per fraction × 28 fractions = 59.92 Gy. Brachytherapy:Dose prescriptions
• Dose: 7.00 Gy per fraction × 4 fractions = 28.0 Gy.

Interventions

Toripalimab

Induction chemo-immunotherapy (platinum-based tri-weekly regimen)

• Paclitaxel 175 mg/m² IV on day 1
• Cisplatin 50 mg/m² IV on day 1 or carboplatin AUC 4-5 IV on day 1
• Toripalimab 240 mg IV on day 1, administered immediately before each chemotherapy infusion Cycle length: every 3 weeks Number of cycles: 2 Concurrent chemoradiotherapy (weekly regimen)
• Radiation therapy delivered according to institutional protocol
• Cisplatin 40 mg/m² IV once weekly
• Toripalimab 240 mg IV on day 1 of every 3-week cycle, given before chemotherapy Cycle length: every 3 weeks during radiotherapy

Maintenance immunotherapy

• Toripalimab 240 mg IV on day 1 every 3 weeks (Q3W) Duration: 1 year (total 13 cycles)

Intervention Type: DRUG

Pelvic External-Beam Radiotherapy (EBRT)

• PTV: 6 MV photons, 1.80 Gy per fraction × 28 fractions = 50.4 Gy.
• PGTVnd: 6 MV photons, 2.14 Gy per fraction × 28 fractions = 59.92 Gy. Brachytherapy:Dose prescriptions
• Dose: 7.00 Gy per fraction × 4 fractions = 28.0 Gy.

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

• Women aged 18-75 years.

• Histologically confirmed, previously untreated locally advanced cervical cancer of squamous, adenocarcinoma, or adenosquamous type.
• At least one measurable lesion that has not received prior local therapy (non-nodal lesion ≥ 10 mm longest diameter or pathological lymph node ≥ 15 mm short axis, per RECIST 1.1).
• Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1.
• Estimated life expectancy ≥ 6 months.
• Investigator-assessed eligibility for concurrent chemoradiotherapy.
• No clinically significant active bleeding.
• Laboratory values: WBC > 4 × 10⁹/L; platelets > 100 × 10⁹/L.
• No history of other malignancies.
• Women of child-bearing potential must have a negative serum pregnancy test and use effective contraception throughout the study.
• Written informed consent obtained prior to any study-related procedures.

Exclusion Criteria

• Tumor recurrence or distant metastasis at screening.

• Active autoimmune disease requiring systemic therapy, or any chronic condition requiring long-term high-dose corticosteroids (≥10 mg/day prednisone or equivalent) or other immunosuppressive agents.
• Systemic corticosteroids (>10 mg/day prednisone or equivalent) or any other immunosuppressive drugs within 14 days before first study dose or anticipated during the study.
• Live-attenuated vaccination within 30 days before first dose or planned during the study.
• Prior organ transplantation or known HIV infection.
• Active hepatitis B (HBV DNA >2000 IU/mL or >10⁴ copies/mL, or HBsAg positive) or active hepatitis C (HCV RNA >10³ copies/mL); co-infection with both viruses is also excluded.
• Prior therapy with any agent targeting PD-1, PD-L1, PD-L2, CD137, CTLA-4 (e.g., ipilimumab), or any other antibody or drug that modulates T-cell co-stimulation or checkpoint pathways.
• Known hypersensitivity to monoclonal antibodies, fusion proteins, or any excipients in the investigational products.
• History of another malignancy within the past 5 years, except adequately treated cervical carcinoma in situ, basal-cell carcinoma of the skin, or other localized malignancies considered cured.
• Severe non-surgical comorbidity or acute infection.
• Peripheral neuropathy > Grade 1 (NCI-CTCAE).
• Inadequate hematologic or organ function:
• WBC < 4.0 × 10⁹/L, ANC < 1.5 × 10⁹/L, platelets < 100 × 10⁹/L, Hb < 90 g/L
• TBIL > 1.5 × ULN, ALT/AST > 2.5 × ULN, BUN > 1.5 × ULN, creatinine > 1.5 × ULN
• Symptomatic brain metastases.
• Clinically significant cardiac arrhythmias, myocardial ischemia, severe conduction block, heart failure, or severe valvular disease.
• Severe bone-marrow failure.
• Uncontrolled psychiatric illness.
• Pregnant or lactating women.
• Investigator-judged unsuitability for the trial.
• Concurrent participation in another interventional clinical study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Tianjin Medical University Cancer Institute and Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Tianjin Medical University Cancer Institute&Hospital

Tianjin, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Jie Chen

Role: CONTACT

tjcjvip@126.com

+86-18622221202

Yuanjie Cao

Role: CONTACT

cyjro325@gmail.com

+86-18522123151

Facility Contacts

Jie Chen

Role: primary

tjcjvip@126.com

+8618622221202

Yuanjie Cao

Role: backup

cyjro325@gmail.com

+86-15510932601

Other Identifiers

E20250419

Identifier Type: -

Identifier Source: org_study_id