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Proton Therapy in Extended-field Irradiation for Cervical Cancer

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

Severe lymphopenia is a common complication of extended-field radiotherapy in cervical cancer, significantly impacting immune function and clinical outcomes. This study aims to evaluate whether proton therapy, with its superior dose distribution, can reduce lymphopenia and improve survival and toxicity profiles compared to photon therapy.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 20
Maximum Age: 85
Healthy Volunteers: f
View:

• Histologically confirmed cervical cancer, stage ≥ IIIC.

• Age between 20 and 85 years.

• Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

• Eligible for extended-field radiotherapy as determined by the treating physician.

• Induction chemotherapy with paclitaxel and carboplatin is allowed if the duration is ≤ 6 weeks or ≤ 2 cycles.

• RT alone, or concurrent single-agent chemotherapy with weekly cisplatin or carboplatin during radiation therapy is allowed, while the use of any other concurrent antineoplastic agents is prohibited.

• Consolidative chemotherapy or immunotherapy after radiation therapy is allowed.

Locations
Other Locations
Taiwan
National Taiwan University Hospital
RECRUITING
Taipei
Chang Gung Memorial Hospital
RECRUITING
Taoyuan
Contact Information
Primary
Jenny Ling-Yu Chen Attending Physician, MD PhD
ntuhrec@ntuh.gov.tw
886-2-23123456
Time Frame
Start Date: 2025-09-30
Estimated Completion Date: 2030-05
Participants
Target number of participants: 44
Treatments
Experimental: Proton extended-field radiotherapy
Proton extended-field radiotherapy
Active_comparator: Photon extended-field radiotherapy
Photon extended-field radiotherapy
Related Therapeutic Areas
Sponsors
Leads: National Taiwan University Hospital

This content was sourced from clinicaltrials.gov

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