Phase 2
N=20
Oxaliplatin and Gemcitabine Followed by Radiation Therapy in the Management of Mixed Mullerian Tumors of the Uterus
Mixed Mullerian Tumors of the Uterus
Bottom Line
View on ClinicalTrials.gov: NCT00476086 ↗Enrolled (actual)
20
Serious AEs
11.8%
Results posted
Apr 2016
Primary outcome: Primary: Chemotherapy Completion Rate — 100 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Gemcitabine (Drug); Oxaliplatin (Drug); Radiation (Radiation)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Dana-Farber Cancer Institute
- Primary completion
- Mar 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Chemotherapy Completion Rate |
100 | — |
| SECONDARY Radiation Therapy Completion Rate |
79 | — |
Summary
The purpose of this research study is to determine the feasibility and safety of giving the combination of oxaliplatin and gemcitabine followed by radiation therapy and to learn whether or not this drug combined with radiation therapy works in treating women with Mullerian tumors of the uterus.
Eligibility Criteria
Inclusion Criteria
- Surgically staged and histologically confirmed diagnosis of MMMT
- 18 years of age or older
- ECOG Performance Score of 0-2
- Adequate bone marrow function
- Adequate renal function
- Adequate hepatic function
- Patients must be recovered from both the acute and late effects of any prior surgery
Exclusion Criteria
- Patients with an active infection
- Patients with CNS metastases
- History of prior malignancy within the past 5 years except curatively treated basal cell carcinoma of the skin, or cervical intraepithelial neoplasia
- Known hypersensitivity to any of the components of oxaliplatin or gemcitabine
- Prior radiation to the pelvis
- Patients who are receiving concurrent investigational therapy or who have received investigational therapy within 30 days
- Peripheral neuropathy greater or equal to Grade 2
- Stage IV visceral disease (lung and liver metastases at presentation)
- Any other medical condition, including mental illness or substance abuse, deemed by the investigator to be likely to interfere with a patient's ability to sign informed consent
- Known HIV or Hepatitis B or C (active, previously treated or both)
- Pregnant or breast feeding
Data sourced from ClinicalTrials.gov (NCT00476086). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.