Trebananib in Treating Patients With Persistent or Recurrent Endometrial Cancer (NCT01210222) | Clinical Trial Compass
CompletedPhase 2
Trebananib in Treating Patients With Persistent or Recurrent Endometrial Cancer
United States35 participantsStarted 2011-06-06
Plain-language summary
This phase II trial studies the side effects and how well trebananib works in treating patients with persistent or recurrent endometrial cancer. Trebananib may stop the growth of endometrial cancer by blocking blood flow to the tumor.
Who can participate
Age range18 Years
SexFEMALE
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Inclusion Criteria:
* Patients must have recurrent or persistent endometrial carcinoma, which is refractory to curative therapy or established treatments; histologic confirmation of the original primary tumor is required; stained slides to document the primary tumor as well as recurrent/persistent disease (if documented by histology or cytology) are required
* Patients with the following histologic epithelial cell types are eligible:
* Endometrioid adenocarcinoma
* Serous adenocarcinoma
* Undifferentiated carcinoma
* Clear cell adenocarcinoma
* Mixed epithelial carcinoma
* Adenocarcinoma not otherwise specified (N.O.S.)
* Mucinous adenocarcinoma
* Squamous cell carcinoma
* Transitional cell carcinoma
* All patients must have measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1; measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded); each lesion must be \>= 10 mm when measured by computed tomography (CT), magnetic resonance imaging (MRI) or caliper measurement by clinical exam; or \>= 20 mm when measured by chest x-ray; lymph nodes must be \>= 15 mm in short axis when measured by CT or MRI
* Patients must have at least one "target lesion" to be used to assess response on this protocol as defined by RECIST 1.1; tumors within a previously irradiated field will be designated as 'non-target" lesions unless progression is documented or …
What they're measuring
1
Progression-free Survival > 6 Months
Timeframe: At 6 months
2
Objective Tumor Response (Complete or Partial Response)