Status:
COMPLETED
Dose-Dense MVAC With Pegfilgrastim Support in Subjects With Muscle-Invasive Urothelial Carcinoma
Lead Sponsor:
Dana-Farber Cancer Institute
Collaborating Sponsors:
Beth Israel Deaconess Medical Center
Brigham and Women's Hospital
Conditions:
Bladder Cancer
Muscle-invasive Bladder Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this research study is to test the effectiveness of neoadjuvant dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin (ddMVAC) in combination with pegfilgrastim followed by r...
Detailed Description
* Participants will be given a study infusion schedule for each treatment cycle. Each treatment cycle lasts three weeks. The infusion of methotrexate will take place on the first day of each cycle. In...
Eligibility Criteria
Inclusion
- Histologic proof of urothelial cancer. Patients with all histologic subtypes are eligible as long as transitional cell carcinoma is predominant, with the exception of more than a few clusters of small cell carcinoma, which is treated with different chemotherapy and thus are ineligible
- Patients with primary tumors arising in the bladder or urethra are eligible if they have clinical T2-T4a disease
- Patients with primary tumors arising in the ureter or renal pelvis are eligible if they have either grade 3 tumors, or radiographic abnormality large enough to be recognized as an abnormal mass by CT/imaging
- Evaluation by a urologist and be deemed to be acceptable surgical candidates within 3 months of registration
- Adequate physiologic reserves as outlined in the protocol
- Clinical or pathologic N1 lymph node involvement (involvement of a single lymph node \< 2cm in greatest dimension) are eligible. Patients with N2-3 or M1 disease are ineligible
- Determination of LV function with an EF \> 50%
- Women of child-bearing potential must have a negative pregnancy test
- Patients of child-bearing or father-bearing potential must agree to use an acceptable form of birth control while on the study
- Patients with prior malignancy are eligible provided that the expected outcome from the prior cancer is such that this will not interfere in the delivery of this therapy, or the assessment of response in the cystectomy specimen
- 18 years of age or older
Exclusion
- Current, recent (within 3 weeks), or planned participation with other experimental anti-cancer medications as part of clinical trials
- Prior treatment with doxorubicin
- Prior systemic cytoreductive chemotherapy for bladder cancer
- Blood pressure of \> 160/100 mmHg. Patients whose blood pressure can be controlled with oral medication are eligible
- NYHA Grade II or greater congestive heart failure
- History of myocardial infarction or unstable angina within 6 months prior to study enrollment
- History of stroke or transient ischemic attack within 6 months prior to study enrollment
- Clinically significant peripheral vascular disease
- Evidence of bleeding diathesis or coagulopathy
- Known history of central nervous system or brain metastases
- Major surgical procedure, significant traumatic injury within 21 days prior to Day 1, or anticipation of need for major surgical procedure during the course of the study
- Lactating women
- Patients who are not candidates for surgery, or unwilling to undergo surgery
- Patients with significant fluid collection
- Known hypersensitivity to any component of cisplatin, methotrexate, vinblastine, doxorubicin or pegfilgrastim
Key Trial Info
Start Date :
December 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2016
Estimated Enrollment :
39 Patients enrolled
Trial Details
Trial ID
NCT00808639
Start Date
December 1 2008
End Date
September 1 2016
Last Update
October 24 2016
Active Locations (4)
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1
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02115
2
Dana-Farber Cancer Institute
Boston, Massachusetts, United States, 02115
3
Lahey Clinic
Burlington, Massachusetts, United States, 01805
4
University of Pittsburgh Cancer Institute
Pittsburgh, Pennsylvania, United States, 15232