Cisplatin
DrugWeekly Cisplatin 35mg/m2 x 6 doses, IV administration
Other names: Cisplatuin Ebewe, Cisplatin Injection
NCT Number: NCT00330499
The purpose of this study is to define the optimal management of localised transitional cell carcinoma (TCC) of the urinary bladder. The main objective is to evaluate whether chemoradiation is superior to radiotherapy alone.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Liverpool Hospital, Liverpool, New South Wales, Australia
Whilst concurrent chemo-radiation is increasingly being looked upon as the treatment of choice for patients referred for bladder preservation, the study by the NCI of Canada (Coppin CM, Gospodarowicz MK et al.Improved Local Control of Invasive Bladder Cancer by Concurrent Cisplatin and Pre-operative or Definitive Radiation.J. of Clinical Oncol. 14(11): 2901-2907, 1996) is the only randomised trial to show some superiority of concurrent Cisplatin and radiation treatment over radiation alone in increasing pelvic tumour control. There was no impact on overall survival. However, this study had relatively small subject numbers and included two distinct treatment options. In one group the patients were treated with a bladder sparing approach and in the other by pre-operative therapy and cystectomy with the type of definitive treatment being decided upon by both the treating Specialist and patient. At 5 years the pelvic failure rates in the radiation alone and chemo-radiation arms were 59% and 40% respectively. With half of the patients in each group having had planned cystectomy as part of their treatment regimen, the above rates of local relapse (especially in the chemo-radiation arm) are disappointing.
Given the concerns with the above study, and the continuing paucity of randomised phase III studies comparing chemo-radiation with radiation alone, there lies an opportunity for Australasian centres to take up the challenge. For this study, the proposed schedule for the chemo-radiation arm is to be the same as that being investigated in our previous phase II study (six weekly doses of Cisplatin plus radiation to a dose of 64Gy in 32 fractions over 6.5 weeks). This will be compared with radical radiation alone (64Gy in 32 fractions over 6.5 weeks).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
If radiological evaluation of a lymph node is interpreted as "positive" this must be evaluated further by either lymph node sampling or percutaneous needle biopsy. Patients with histologically confirmed lymph node metastases will not be eligible.
N.B. Previous:
does not exclude the patient from being eligible. However, the patient should have an adequate functioning bladder (this should be clarified with the referring Urologist and if need be voiding volumes should be measured).
Exclusion criteria
Weekly Cisplatin 35mg/m2 x 6 doses, IV administration
Other names: Cisplatuin Ebewe, Cisplatin Injection
64Gy reference dose in 32 fractions over 6.5 weeks
Other names: Radiation
Time frame: 3 years
Time frame: 3 months
Time frame: Final analysis when all patients have been followed for 3 years. (approx. 7 years from start of trial)
Time frame: Final analysis when all patients have been followed for 3 years. (approx. 7 years from start of trial)
Time frame: Final analysis when all patients have been followed for 3 years. (approx. 7 years from start of trial)
Time frame: Interim analyses will be performed on an annual basis.
Time frame: Final analysis when all patients have been followed for 3 years. (approx. 7 years from start of trial)
Time frame: Final analysis when all patients have been followed for 3 years. (approx. 7 years from start of trial)
Trans Tasman Radiation Oncology Group
Other
A Randomised Trial of Radical Chemo/Radiotherapy vs Radiotherapy Alone in the Definitive Management of Localised Muscle Invasive TCC of the Urinary Bladder
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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