Usefulness of FDG-PET for Advanced Cervical Cancer (NCT00146458) | Clinical Trial Compass
UnknownPhase 3
Usefulness of FDG-PET for Advanced Cervical Cancer
Taiwan200 participantsStarted 2002-01
Plain-language summary
The objective of this study is to determinate whether the adding of FDG-PET is helpful in the treatment of advanced cervical cancer with concurrent chemoradiation.
Who can participate
Age range0 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Newly diagnosed cervical cancer clinical stage FIGO I -IVA
* Histologically proven cervical carcinoma (including histologic types of squamous cell carcinoma, adenocarcinoma, adenosquamous carcinoma, adenoid cystic carcinoma, lymphoepithelial-like carcinoma and malignant mixed mullerian tumor)
* Presence of at least one enlarged pelvic lymph node (\>=1.0 cm in its maximal dimension), or group of small pelvic nodes (size \<1 cm), and without suspicious para-aortic lymph node metastasis or any lesion outside the pelvis by conventional MRI or CT study
* Karnofsky performance scale \>=60
* Available for concurrent chemoradiation therapy of curative intent
Exclusion Criteria:
* Cervical tumor with histologic diagnosis of verrucous carcinoma or small cell carcinoma
* Other serious illness or medical condition which would interfere with extended field irradiation or chemotherapy
* Past or current history of malignancy, except for curatively treated non-melanoma skin cancer
* Patients not suitable to receive PET study either by technical or psychological reasons
* Patients who are judged to be noncompliant to treatment or not accessible for follow up
What they're measuring
1
The difference of disease-free-survival and overall-survival with/ without FDG-PET at two years after treatment