Pembrolizumab Concurrent With and Following Carbon-ion Radiotherapy for Locally Advanced Cervical Adenocarcinoma

NCT06805864 | Not Yet Recruiting Phase 2 DMC

• 1 other identifier: IRB2024-049
• Study Type: interventional
• Target: 45
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this clinical trial is to learn if pembrolizumab works for cervical adenocarcinoma treat with concurrent chemo-carbon-ion radiaotherapy (CIRT). The main questions it aims to answer are: • Does concurrent chemo-CIRT with pembrolizumab improves 2-year progression-free survival (PFS), compared with concurrent chemoradiotherapy with conventional X-rays?

Conditions

Cervical Adenocarcinoma; Cervical Adenosquamous Carcinoma

Keywords

Cervical Cancer; Carbon-ion Radiotherapy; Pembrolizumab

Outcome Measures

Primary Outcomes (1)

• Progression-free survival (PFS)

  It is based on the investigator's RECIST 1.1 assessment, or in the absence of imaging evidence of disease progression based on RECIST 1.1, histologically confirmed PD, after concurrent chemo-CIRT with pembrolizumab.

  At 2 years after the start of trial treatment

Secondary Outcomes (4)

• Overall survival (OS)

  At 2 years after the start of trial treatment

• Complete response (CR) rate

  At 6 months after the start of trial treatment

• Local control (LC)

  At 2 years after the start of trial treatment

• Acute and late toxicities

  Acute (≤ 90 days) and late toxicities (> 90 days) over 2 years after the start of trial treatment.

Study Arms (1)

CIRT＋CDDP＋Pembro

EXPERIMENTAL

Patients will first be treated with 16 fractions/4 weeks of carbon-ion radiation therapy (CIRT) followed by 3 cycles/2 weeks of image-guided brachytherapy (IGBT). During this radiation therapy, up to 5 cycles of weekly cisplatin will be given concurrently. In addition to these, pembrolizumab will be administered every 3 weeks at 200 mg for the first 2 cycles, then increased to 400 mg every 6 weeks for 17 cycles over 2 years.

Drug: Pembrolizumab (KEYTRUDA®)

Interventions

Pembrolizumab (KEYTRUDA®) DRUG

Pembrolizumab is administered at 200 mg every 3 weeks for the first 2 cycles during Chemo-CIRT, after completion of radiotherapy, the dose is increased to 400 mg and given every 6 weeks for a total of 17 cycles over 2 years.

CIRT＋CDDP＋Pembro

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• \. Female participants who are at least 18 years of age on the day of signing informed consent with histologically confirmed adenocarcinoma or adenosquamous carcinoma of the uterine cervix and Stage ⅡA2, ⅡB, ⅢA, ⅢB, ⅢC1r, IVA according to FIGO classification (2018) will be enrolled in this study.
• \. The participant (or legally acceptable representative if applicable) provides written informed consent for the trial.
• \. Have measurable disease based on RECIST 1.1.
• \. Archival tumor tissue sample or a newly obtained biopsy of a tumor lesion that was not previously irradiated was provided. Formalin-fixed, paraffin-embedded (FFPE) tissue blocks are preferred to slides. Newly obtained biopsy samples are preferred to archived tissues.
• \. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1. Evaluation of ECOG is to be performed within 7 days prior to the first dose of pembrolizumab.
• \. Have adequate organ function below. Specimens must be collected within 10 days to the start of pembrolizumab administration.
• Absolute neutrophil count (ANC) ≥ 1500/µL, Platelets ≥ 100000/µ, Hemoglobin ≥9.0 g/dL or ≥ 5.6 mmol/L, Creatinine clearance ≥ 50 mL/min, Total bilirubin ≤1.5 ×ULN or direct bilirubin ≤ULN for participants with total bilirubin levels \>1.5 × ULN, AST and ALT ≤2.5 × ULN, International normalized ratio (INR) OR prothrombin time (PT) Activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN unless participant is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants.

You may not qualify if:

• \. Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX-40, CD137).
• \. Has received prior radical surgery, RT, or systemic therapy (including investigational drugs) for cervical cancer. Note: Conization for localized cervical tumors is allowed.
• \. Has received a live vaccine or live-attenuated vaccine within 30 days before the first dose of study intervention. Administration of killed vaccines is allowed.
• Note: please refer to Section 5.3 for information on COVID-19 vaccines
• \. Has received an investigational agent or has used an investigational device within 4 weeks prior to pembrolizumab administration.
• \. Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of pembrolizumab.
• \. Known additional malignancy that is progressing or has required active treatment within the past 3 years.
• Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ, excluding carcinoma in situ of the bladder, that have undergone potentially curative therapy are not excluded.
• \. Has severe hypersensitivity (≥ Grade 3) to pembrolizumab and/or any of its excipients.
• \. Has active autoimmune disease that has required systemic treatment in the past 2 years except replacement therapy (e.g.., thyroxine, insulin, or physiologic corticosteroid).
• \. Has a history of (non-infectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease.
• \. Has an active infection requiring systemic therapy.
• \. History of active Hepatitis B (defined as HBsAg reactive) or known active Hepatitis C virus (defined as detectable HCV RNA \[qualitative\]) infection.
• \. Has a history or current evidence of any condition, therapy, or laboratory abnormality or other circumstance that might confound the results of the study, interfere with the participant's participation for the full duration of the study, such that it is not in the best interest of the participant to participate, in the opinion of the treating investigator.
• \. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.

Sponsors & Collaborators

• Gunma University: lead
• Merck Sharp & Dohme LLC: collaborator

Study Sites (1)

Gunma University Hospital

Maebashi, Gunma, 371-8511, Japan

Location

MeSH Terms

Conditions

Uterine Cervical Neoplasms

Interventions

pembrolizumab

Condition Hierarchy (Ancestors)

Uterine Neoplasms; Genital Neoplasms, Female; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Uterine Cervical Diseases; Uterine Diseases; Genital Diseases, Female; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Genital Diseases

Central Study Contacts

Tatsuya Ohno, M.D., Ph.D.

CONTACT

+81-27-220-8383; tohno@gunma-u.ac.jp

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor, Department of Radiation Oncology

Study Record Dates

• First Submitted: January 28, 2025
• First Posted: February 3, 2025
• Study Start: February 1, 2025
• Primary Completion (Estimated): December 31, 2029
• Study Completion (Estimated): December 31, 2030
• Last Updated: February 3, 2025

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

JP (1)