Neoadjuvant Chemotherapy Plus Nephroureterectomy for Locally Advanced Upper Tract Transitional Cell Cancer
Primary Purpose
Transitional Cell Carcinoma
Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Gemcitabine and cisplatin
Retrospective comparison
Sponsored by
About this trial
This is an interventional treatment trial for Transitional Cell Carcinoma focused on measuring Upper GU Tract Transitional Cell Carinoma, Nephroureterectomy, Chemotherapy, Gemcitabine, Cisplatin
Eligibility Criteria
Inclusion Criteria:
- ECOG performance status 0-2
- Estimated GFR>60
- High grade TCC on initial biopsy
- Clinical stage T1-T3, Nx, Mx based on the AJCC Classification system
- TCC confined to the ureter or renal pelvis
- Grade II neuropathy or less
Exclusion Criteria:
- Any other malignancy over the previous five years with a risk of relapse that exceeds 30%
- History of previous cystectomy
- Evidence of metastatic disease
- History of pelvic irradiation or prior chemotherapy
Sites / Locations
- Lahey Clinic, Inc.
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
1
2
Arm Description
A neoadjuvant chemotherapy (gemcitabine and cisplatin) regimen administered before surgery-nephroureterectomy for upper tract TCC
A retrospective cohort group (approximately 60 subjects) identified from an institutional cancer registry who have undergone a nephroureterectomy alone over the past five years
Outcomes
Primary Outcome Measures
Neoadjuvant chemotherapy (Gemcitabine and Cisplatin) Regime (3 cycles) before Nephroureterectomy
Secondary Outcome Measures
Overall survival compared to institutional historical cohort of subjects who have undergone a nephroureterectomy alone.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00696007
Brief Title
Neoadjuvant Chemotherapy Plus Nephroureterectomy for Locally Advanced Upper Tract Transitional Cell Cancer
Official Title
Neoadjuvant Chemotherapy Plus Nephroureterectomy for Locally Advanced Upper Tract Transitional Cell Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Withdrawn
Why Stopped
Study was unable to recruit subjects meeting the study requirements.
Study Start Date
April 2008 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lahey Clinic
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to test the effectiveness, safety and side effects of two chemotherapy drugs (gemcitabine and cisplatin) when combined with surgery after chemotherapy for patients with upper urinary tract cancer. The hypothesis is that undergoing chemotherapy prior to surgery will have a beneficial effect on prognosis and may improve overall survival as in patients with bladder cancer, and will allow better tolerance of chemotherapy than if it were given after surgery.
Detailed Description
This study will look at improving overall survival of those undergoing nephroureterectomy for upper tract TCC (transitional cell carcinoma, comparing the pathological response of tumors treated with Neoadjuvant Chemotherapy (gemcitabine and cisplatin) before surgery. There have been reported studies of neoadjuvant chemotherapy in the treatment of upper tract TCC, there have been no studies to date that include the chemotherapy agents gemcitabine and cisplatin that are currently indicated in treating TCC of the bladder in the neoadjuvant and adjuvant setting. These agents have been proven to have a better overall safety profile and tolerability allowing more patients to complete their regimens. Secondarily, study will compare disease free overall survival among patients treated with neoadjuvant chemotherapy and surgery versus surgery alone. This study may elucidate the potential benefit of these agents when treating TCC of the upper tracts and may provide a survival advantage in this specific patient population as compared to a historical cohort.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Transitional Cell Carcinoma
Keywords
Upper GU Tract Transitional Cell Carinoma, Nephroureterectomy, Chemotherapy, Gemcitabine, Cisplatin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
A neoadjuvant chemotherapy (gemcitabine and cisplatin) regimen administered before surgery-nephroureterectomy for upper tract TCC
Arm Title
2
Arm Type
Other
Arm Description
A retrospective cohort group (approximately 60 subjects) identified from an institutional cancer registry who have undergone a nephroureterectomy alone over the past five years
Intervention Type
Drug
Intervention Name(s)
Gemcitabine and cisplatin
Other Intervention Name(s)
Neoadjuvant Chemotherapy
Intervention Description
Neoadjuvant chemotherapy (gemcitabine and cisplatin) administered before Nephroureterectomy.
Chemotherapy regimen of three cycles of gemcitabine and cisplatin, dosed over a 3 month period Each cycle would consist of gemcitabine and cisplatin on day 1, with two other doses of gemcitabine on day 8 and day 15.
Gemcitabine dosing would be 1,000 mg/m² and cisplatin would be dosed at 70 mg/m²
Intervention Type
Other
Intervention Name(s)
Retrospective comparison
Intervention Description
60 retrospective historical cohort group of subjects who have undergone a radical nephroureterectomy over the past five years
Primary Outcome Measure Information:
Title
Neoadjuvant chemotherapy (Gemcitabine and Cisplatin) Regime (3 cycles) before Nephroureterectomy
Time Frame
5 years: follow ups 1st year/every 4 mths, 2nd & 3rd year to every 6 months, 4th & 5th yr-annually for patients who remain disease free
Secondary Outcome Measure Information:
Title
Overall survival compared to institutional historical cohort of subjects who have undergone a nephroureterectomy alone.
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ECOG performance status 0-2
Estimated GFR>60
High grade TCC on initial biopsy
Clinical stage T1-T3, Nx, Mx based on the AJCC Classification system
TCC confined to the ureter or renal pelvis
Grade II neuropathy or less
Exclusion Criteria:
Any other malignancy over the previous five years with a risk of relapse that exceeds 30%
History of previous cystectomy
Evidence of metastatic disease
History of pelvic irradiation or prior chemotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher G. Tretter, M.D.
Organizational Affiliation
Lahey Clinic, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lahey Clinic, Inc.
City
Burlington
State/Province
Massachusetts
ZIP/Postal Code
01805
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
1433610
Citation
Splinter TA, Pavone-Macaluso M, Jacqmin D, Roberts JT, Carpentier P, de Pauw M, Sylvester R. A European Organization for Research and Treatment of Cancer--Genitourinary Group phase 2 study of chemotherapy in stage T3-4N0-XM0 transitional cell cancer of the bladder: evaluation of clinical response. J Urol. 1992 Dec;148(6):1793-6. doi: 10.1016/s0022-5347(17)37031-3.
Results Reference
background
PubMed Identifier
17320658
Citation
Raman JD, Sosa RE, Vaughan ED Jr, Scherr DS. Pathologic features of bladder tumors after nephroureterectomy or segmental ureterectomy for upper urinary tract transitional cell carcinoma. Urology. 2007 Feb;69(2):251-4. doi: 10.1016/j.urology.2006.09.065.
Results Reference
background
PubMed Identifier
17125474
Citation
Brown GA, Busby JE, Wood CG, Pisters LL, Dinney CP, Swanson DA, Grossman HB, Pettaway CA, Munsell MF, Kamat AM, Matin SF. Nephroureterectomy for treating upper urinary tract transitional cell carcinoma: Time to change the treatment paradigm? BJU Int. 2006 Dec;98(6):1176-80. doi: 10.1111/j.1464-410X.2006.06524.x.
Results Reference
background
PubMed Identifier
8976209
Citation
Keeley FX, Kulp DA, Bibbo M, McCue PA, Bagley DH. Diagnostic accuracy of ureteroscopic biopsy in upper tract transitional cell carcinoma. J Urol. 1997 Jan;157(1):33-7.
Results Reference
background
PubMed Identifier
9763077
Citation
Hall MC, Womack S, Sagalowsky AI, Carmody T, Erickstad MD, Roehrborn CG. Prognostic factors, recurrence, and survival in transitional cell carcinoma of the upper urinary tract: a 30-year experience in 252 patients. Urology. 1998 Oct;52(4):594-601. doi: 10.1016/s0090-4295(98)00295-7.
Results Reference
background
PubMed Identifier
12944571
Citation
Grossman HB, Natale RB, Tangen CM, Speights VO, Vogelzang NJ, Trump DL, deVere White RW, Sarosdy MF, Wood DP Jr, Raghavan D, Crawford ED. Neoadjuvant chemotherapy plus cystectomy compared with cystectomy alone for locally advanced bladder cancer. N Engl J Med. 2003 Aug 28;349(9):859-66. doi: 10.1056/NEJMoa022148. Erratum In: N Engl J Med. 2003 Nov 6;349(19):1880.
Results Reference
background
PubMed Identifier
8533199
Citation
Igawa M, Urakami S, Shiina H, Kishi H, Himeno Y, Ishibe T, Kadena H, Usui T. Neoadjuvant chemotherapy for locally advanced urothelial cancer of the upper urinary tract. Urol Int. 1995;55(2):74-7. doi: 10.1159/000282755.
Results Reference
background
Learn more about this trial
Neoadjuvant Chemotherapy Plus Nephroureterectomy for Locally Advanced Upper Tract Transitional Cell Cancer
We'll reach out to this number within 24 hrs