Papillary Serous Carcinoma of the Endometrium
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Purpose
Primary Objectives:
- To evaluate the results of Paclitaxel and pelvic radiation in pelvic confined papillary serous carcinoma of the endometrium for both local control and overall survival.
- To evaluate the toxicity of Paclitaxel and pelvic radiation.
- To collect and evaluate patients' quality of life/symptom assessment data.
| Condition | Intervention | Phase |
|---|---|---|
|
Endometrial Cancer |
Drug: Paclitaxel Radiation: Pelvic Radiation |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase II Study: Paclitaxel and Pelvic Radiation for Stage I-IIIA Papillary Serous Carcinoma of the Endometrium |
- Overall Survival [ Time Frame: Continual Assessments (every 3 months for 1 year, then every 4 months for 2 years, then every 6 months for 2 years, then once a year) ] [ Designated as safety issue: No ]
| Enrollment: | 30 |
| Study Start Date: | April 2001 |
| Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Paclitaxel (Taxol) + Pelvic Radiation
Paclitaxel (Taxol) 50 mg/m^2 IV Weekly Over 1 Hour x 5 Weeks. Radiation therapy to the pelvis daily for 25 treatments.
|
Drug: Paclitaxel
50 mg/m^2 IV Weekly Over 1 Hour x 5 Weeks
Other Name: Taxol
Radiation: Pelvic Radiation
Radiation therapy to the pelvis daily for 25 treatments.
|
Hide Detailed DescriptionDetailed Description:
Paclitaxel is designed to block the mechanisms of cell division in cancer cells, which may cause them to die.
Before you can start treatment on this study, you will have "screening tests." These tests will help the doctor decide if you are eligible to take part in this study. You will have a complete physical exam, including measurement of your height, weight, and body surface area. Your complete medical history will be recorded. Your cancer diagnosis will be confirmed by checking tissue slides from the tissue removed during yoru surgery. You will have blood drawn (about 1 tablespoon) for routine tests, tests of your liver function, and CA-125 levels. You will also have chest x-rays, a computed tomography (CT) scan of your chest, and either a CT or magnetic resonance imaging (MRI) scan of your abdomen and pelvis. These scans should be performed within 6 weeks before starting study treatment.
If you are found to be eligible to take part in this study, you will begin treatment. You will have radiation treatment to your pelvis (hip area) every day (Monday - Friday) for a total of 25 treatments. Each treatment should take about 20 minutes to complete.
After the radiation treatment, you will receive a type of radiation called a "vaginal cuff boost." The vaginal cuff boost involves a small device being inserted into the vagina to treat the back of the vagina with a high dose of radiation. The applicator is similar to placing a large tampon in the vagina. This internal treatment takes about 30 minutes for each treatment. This is separate from the external radiation treatments that are given.
While you are receiving radiation treatment, and then afterwards, you will also receive chemotherapy with paclitaxel. During the radiation period, you will receive paclitaxel by vein over 1 hour, on Days 1, 8, 15, 22, and 29. Starting 4-6 weeks after radiation treatment is finished, you will receive paclitaxel at a larger dose, given over 3 hours each time, once every 21 days (3 weeks). You will receive up to 4 "cycles" of chemotherapy, each cycle lasting 21 days.
You will be given certain drugs about 30 minutes before your chemotherapy treatments to help control possible side effects, like allergic reactions. These drugs include dexamethasone, diphenhydramine (Benadryl), and cimetidine.
You will have several tests performed throughout the study. Before each cycle of chemotherapy and one month after the last cycle of chemotherapy is given, quality of life and symptom assessment forms will be completed. These questionnaires should only take about 15 minutes to complete.
While you are on chemotherapy treatment, you will have tests performed before each chemotherapy treatment. This will involve blood (about 1 tablespoon) drawn for routine tests, and a review of your symptoms by the study staff.
Once you are off study treatment, you will be asked to return to the clinic for follow-up visits. These visits will occur every 3 months for 1 year, then every 4 months for 2 years, then every 6 months for 2 years, then once a year after that. At these visits, you will have a physical and pelvic exam performed, along with blood (about 1 tablespoon) drawn for routine tests. Chest x-rays will usually be done once a year and any other diagnostic exams will only be done if your doctor thinks they are needed.
This is an investigational study. There are no standard treatments for this type of endometrial cancer, but radiation and chemotherapy are common treatments. This combination of chemotherapy and radiation is considered experimental. Up to 49 patients will take part in this multicenter study. Up to 44 participants will be enrolled at M. D. Anderson.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patient must undergo surgical staging within 8 weeks of study entry.
- Patients with mixed histology tumor that include a papillary serous component are eligible.
- Only patients with non-measurable disease can be entered.
- Patients may not have had previous chemotherapy or radiation therapy.
- Patients must have an estimated life expectancy of 12 weeks or greater.
- Patients must have a Zubrod performance status of less than or equal to 2.
- Patients must have adequate bone marrow, renal and hepatic function: with WBC greater than or equal to 3000; ANC greater than or equal to 1500; Platelets greater than or equal to 100,000; SGPT less than or equal to 2x the upper limit of normal; Total bilirubin less than or equal to 2.5mg/dl.
- Patients must sign an institutionally approved consent form
Exclusion Criteria:
- Previously treated papillary serous carcinoma with either chemotherapy or radiation therapy.
- Newly diagnosed papillary serous carcinoma of the endometrium, Stage IIIB-IV (patients with disease outside the pelvis).
- Patients who have a history of other malignancy, with the exception of non-melanomatous skin cancer, unless in complete remission and off all therapy for that disease for a minimum of 5 years.
- Patients with a Zubrod status of 3 or greater.
- Patients with an active infection.
- Patients with serious intercurrent medical illness.
- Patients with a recent (within 6 months) history of congestive heart failure, unstable angina or myocardial infarction.
Contacts and Locations| United States, Florida | |
| M. D. Anderson Cancer Center - Orlando | |
| Orlando, Florida, United States, 32806 | |
| United States, Texas | |
| UT MD Anderson Cancer Center | |
| Houston, Texas, United States, 77030 | |
| Principal Investigator: | Anuja Jhingran, MD | M.D. Anderson Cancer Center |
More Information
Additional Information:
No publications provided
| Responsible Party: | M.D. Anderson Cancer Center |
| ClinicalTrials.gov Identifier: | NCT00515073 History of Changes |
| Other Study ID Numbers: | ID00-418 |
| Study First Received: | August 9, 2007 |
| Last Updated: | May 6, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by M.D. Anderson Cancer Center:
|
Endometrial Cancer Papillary Serous Carcinoma Pelvic Radiation Therapy Paclitaxel Taxol |
Additional relevant MeSH terms:
|
Carcinoma Endometrial Neoplasms Cystadenocarcinoma, Serous Adenoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Uterine Neoplasms Genital Neoplasms, Female Urogenital Neoplasms Neoplasms by Site Uterine Diseases Genital Diseases, Female |
Cystadenocarcinoma Adenocarcinoma Neoplasms, Cystic, Mucinous, and Serous Paclitaxel Tubulin Modulators Antimitotic Agents Mitosis Modulators Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Antineoplastic Agents, Phytogenic Antineoplastic Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 22, 2013