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Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12607000041459
Ethics application status
Approved
Date submitted
22/12/2003
Date registered
22/12/2003
Date last updated
12/07/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
Efficacy study of adding chemotherapy to radiotherapy for treating bladder cancer
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Scientific title
Trans Tasman Radiation Oncology Group (TROG) 02.03 - Multicentre Phase III study comparing Radical Synchronous Chemo-Radiation (cisplatin) vs Radical Radiation Alone in the Definitive Management of Muscle Invasive Transitional Cell Carcinoma (TCC) of the Urinary Bladder Following Maximal Trans-Urethral Resection to reduce invasive local failure.
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Secondary ID [1]
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ClinicalTrials.gov: NCT00330499
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Secondary ID [2]
48
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National Clinical Trials Registry: NCTR476
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Universal Trial Number (UTN)
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Trial acronym
TROG 02.03
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Transitional Cell Carcinoma of Urinary bladder
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Condition category
Condition code
Cancer
51
51
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0
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Bladder
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
ARM A: Synchronous chemo/radiation therapy. Weekly infusional cisplatin 35mg/m sqaured x 6 doses plus radiation 64Gy/32 fractions over 6 1/2 weeks.
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Intervention code [1]
1301
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Treatment: Drugs
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Comparator / control treatment
ARM B: Radiation alone. 64Gy/32 fractions over 6 1/2 weeks.
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Control group
Active
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Outcomes
Primary outcome [1]
84
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Invasive local failure
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Assessment method [1]
84
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Timepoint [1]
84
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At 3 years
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Secondary outcome [1]
162
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1. Complete response rate
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Assessment method [1]
162
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Timepoint [1]
162
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At 3mths from randomisation.
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Secondary outcome [2]
163
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2. Disease free survival.
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Assessment method [2]
163
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Timepoint [2]
163
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Time from randomisation to failure or death. Measured until death.
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Secondary outcome [3]
164
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3. Overall survival.
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Assessment method [3]
164
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Timepoint [3]
164
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Time from randomisation to death from any cause. Measured unitl death.
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Secondary outcome [4]
165
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4. Acute and late toxicity.
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Assessment method [4]
165
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Timepoint [4]
165
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Measured every 3 months for the first yr, 6 monthly until 3 yrs and then yearly until death.
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Secondary outcome [5]
166
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5. Pattern of failure. Local failure, regioanl failure, distant failure and death are anaylsed.
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Assessment method [5]
166
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Timepoint [5]
166
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Measured every 3 months for the first yr, 6 monthly until 3 yrs and then yearly until death.
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Secondary outcome [6]
167
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6. Quality of Life measures.
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Assessment method [6]
167
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Timepoint [6]
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Measured pre treatment, week 7 at the end of treatment, 3mths, 12 months post treatment and 2 years post treatment.
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Eligibility
Key inclusion criteria
1. Histologically proven Transitional Cell Carcinoma (TCC) of the urinary bladder. Mixed tumours comprising predominantly TCC and elements of squamous or adenomatous metaplasia or carcinoma are also eligible.
2. Clinically and radiologically localised T2, T3 or T4a non-bulky disease (<= 7cm in maximum dimension), N0, M0.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.
3. Maximal Trans Urethral Resection (TUR). N.B. Previous: a) partial cystectomy; b) endoscopic resection of bladder tumour/s; c) intravesical chemotherapy; or d) intravesical Bacillus Calmette-Guerin (BCG)
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).
4. Creatinine clearance >= 50ml/minute by calculation or measurement.
5. A white blood cell count >= 3.5 x 109/L with an absolute neutrophil count >= 1.5 x 109/L and a platelet count >= 100 x 109/L
6. Eastern Cooperative Oncology Group status of 0, 1 or 2.
7. No age limit applies provided the patient is mentally, physically and geographically capable of undergoing treatment and follow-up.
8. No significant intercurrent morbidity.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Pure squamous carcinomas or adenocarcinomas.
2. Extensive or multifocal Carcinoma In Situ (CIS) change in the bladder.
3. T3 or T4a tumours unsuitable for curative treatment (i.e. > 7cm in any dimension), T4b, node positive and metastatic disease.
4. Presence of ureteric obstruction due to tumour infiltration at the Ureteral Orifice (UO) not amenable to stenting.
5. Previous radiation treatment to the pelvis.
6. Previous significant pelvic surgery.
7. Significant bowel or gynaecological inflammatory disease.
8. Creatinine clearance < 50ml/minute by calculation or measurement. A white blood cell count < 3.5 x 109/L with an absolute neutrophil count < 1.5 x 109L and/or a platelet count < 100 x 109/L.
9. Other considerations making patient unfit for Cisplatin therapy.
10. Prior or concurrent malignancy of any other site unless disease-free for greater than 5 years, except for:1. non-melanoma skin cancer, and/or 2. a) Stage T1 well differentiated prostatic carcinoma in men, and b) In situ carcinoma of the cervix in women.
11. Bladder tumour – biopsy only. These patients must be referred back for more adequate resections or else should not be included.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Central randomisation
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Stratified allocation. Factors: Stage T2/T3/T4a, Complete Trans Urethral resection only, Centre. Simple randomisation by computer.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
11/10/2002
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Actual
11/10/2002
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Date of last participant enrolment
Anticipated
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Actual
11/11/2007
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Date of last data collection
Anticipated
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Actual
9/02/2010
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Sample size
Target
150
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Accrual to date
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Final
67
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment outside Australia
Country [1]
386
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New Zealand
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State/province [1]
386
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Funding & Sponsors
Funding source category [1]
73
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Government body
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Name [1]
73
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National Health & Medical Research Council Project Grant
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Address [1]
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Level 5, 20 Allara St Canberra ACT 2601
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Country [1]
73
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Australia
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Primary sponsor type
Individual
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Name
Kumar Gogna
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Address
Mater QRI Raymond Terrace SOUTH BRISBANE QLD 4101
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Country
Australia
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Secondary sponsor category [1]
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Other Collaborative groups
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Name [1]
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Trans Tasman Radiation Oncology Group (TROG)
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Address [1]
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Edith St Waratah NSW 2298
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Country [1]
59
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
542
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William Buckland radiotherapy Centre, The Alfred
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Ethics committee address [1]
542
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Prahran, VIC
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Ethics committee country [1]
542
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Australia
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Date submitted for ethics approval [1]
542
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Approval date [1]
542
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31/05/2002
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Ethics approval number [1]
542
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Ethics committee name [2]
543
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Auckland Hospital
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Ethics committee address [2]
543
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Auckland, NZ
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Ethics committee country [2]
543
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New Zealand
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Date submitted for ethics approval [2]
543
0
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Approval date [2]
543
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Ethics approval number [2]
543
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Ethics committee name [3]
544
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Campbelltown Hospital
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Ethics committee address [3]
544
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Campbelltown, NSW
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Ethics committee country [3]
544
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Australia
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Date submitted for ethics approval [3]
544
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Approval date [3]
544
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Ethics approval number [3]
544
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Ethics committee name [4]
545
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Christchurch Hospital
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Ethics committee address [4]
545
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Christchurch, NZ
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Ethics committee country [4]
545
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New Zealand
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Date submitted for ethics approval [4]
545
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Approval date [4]
545
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Ethics approval number [4]
545
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Ethics committee name [5]
546
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Dunedin Hospital
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Ethics committee address [5]
546
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Dunedin, NZ
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Ethics committee country [5]
546
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New Zealand
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Date submitted for ethics approval [5]
546
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Approval date [5]
546
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Ethics approval number [5]
546
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Ethics committee name [6]
547
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Premion Tugun
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Ethics committee address [6]
547
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Ethics committee country [6]
547
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Australia
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Date submitted for ethics approval [6]
547
0
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Approval date [6]
547
0
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Ethics approval number [6]
547
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Ethics committee name [7]
548
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Andrew Love Cancer centre, Geelong Hospital
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Ethics committee address [7]
548
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Geelong, VIC
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Ethics committee country [7]
548
0
Australia
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Date submitted for ethics approval [7]
548
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Approval date [7]
548
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Ethics approval number [7]
548
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Ethics committee name [8]
549
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Launceston Hospital
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Ethics committee address [8]
549
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Launceston, TAS
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Ethics committee country [8]
549
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Australia
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Date submitted for ethics approval [8]
549
0
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Approval date [8]
549
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Ethics approval number [8]
549
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Ethics committee name [9]
550
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Liverpool Hospital
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Ethics committee address [9]
550
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Liverpool, NSW
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Ethics committee country [9]
550
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Australia
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Date submitted for ethics approval [9]
550
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Approval date [9]
550
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Ethics approval number [9]
550
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Ethics committee name [10]
551
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Mater QRI
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Ethics committee address [10]
551
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South Brisbane, QLD
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Ethics committee country [10]
551
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Australia
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Date submitted for ethics approval [10]
551
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Approval date [10]
551
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Ethics approval number [10]
551
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Ethics committee name [11]
552
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Nepean Hospital
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Ethics committee address [11]
552
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Penrith, NSW
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Ethics committee country [11]
552
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Australia
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Date submitted for ethics approval [11]
552
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Approval date [11]
552
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Ethics approval number [11]
552
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Ethics committee name [12]
553
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Calvary Mater Newcastle
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Ethics committee address [12]
553
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Waratah, NSW
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Ethics committee country [12]
553
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Australia
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Date submitted for ethics approval [12]
553
0
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Approval date [12]
553
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Ethics approval number [12]
553
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Ethics committee name [13]
554
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Palmerston North
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Ethics committee address [13]
554
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Papaioea, Manawatu-Wanganui, NZ
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Ethics committee country [13]
554
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Australia
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Date submitted for ethics approval [13]
554
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Approval date [13]
554
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Ethics approval number [13]
554
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Ethics committee name [14]
555
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Peter MacCallum Cancer Centre
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Ethics committee address [14]
555
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Melbourne, VIC
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Ethics committee country [14]
555
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Australia
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Date submitted for ethics approval [14]
555
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Approval date [14]
555
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Ethics approval number [14]
555
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Ethics committee name [15]
556
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Prince of Wales Hospital
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Ethics committee address [15]
556
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Randwick, NSW
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Ethics committee country [15]
556
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Australia
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Date submitted for ethics approval [15]
556
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Approval date [15]
556
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Ethics approval number [15]
556
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Ethics committee name [16]
557
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Royal Adelaide Hospital
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Ethics committee address [16]
557
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Adelaide, SA
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Ethics committee country [16]
557
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Australia
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Date submitted for ethics approval [16]
557
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Approval date [16]
557
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Ethics approval number [16]
557
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Ethics committee name [17]
558
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Royal Brisbane and Women's Hospital
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Ethics committee address [17]
558
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Herston, QLD
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Ethics committee country [17]
558
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Australia
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Date submitted for ethics approval [17]
558
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Approval date [17]
558
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Ethics approval number [17]
558
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Ethics committee name [18]
559
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Royal Perth Hospital
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Ethics committee address [18]
559
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Perth, WA
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Ethics committee country [18]
559
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Australia
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Date submitted for ethics approval [18]
559
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Approval date [18]
559
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Ethics approval number [18]
559
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Ethics committee name [19]
560
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Sir Charles Gairdner Hospital
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Ethics committee address [19]
560
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Nedlands, WA
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Ethics committee country [19]
560
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Australia
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Date submitted for ethics approval [19]
560
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Approval date [19]
560
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Ethics approval number [19]
560
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Ethics committee name [20]
561
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Wellington Hospital
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Ethics committee address [20]
561
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Wellington, NZ
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Ethics committee country [20]
561
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New Zealand
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Date submitted for ethics approval [20]
561
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Approval date [20]
561
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Ethics approval number [20]
561
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Ethics committee name [21]
562
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Westmead Hospital
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Ethics committee address [21]
562
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Wentworthville, NSW
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Ethics committee country [21]
562
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Australia
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Date submitted for ethics approval [21]
562
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Approval date [21]
562
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Ethics approval number [21]
562
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Summary
Brief summary
Radiation and chemotherapy both work in people with muscle-invasive bladder cancer. This study will determine if giving them together improves the results for people with this disease that seems to be confined to the bladder, but who are felt to be suitable candidates for bladder preserving treatment.
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Trial website
www.trog.com.au
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Trial related presentations / publications
Abstract 65: Gogna K. TROG 02.03: Intergroup Phase III Randomised Study, Chemotherapy vs radiation alone: Compliance, Toxicity, Quality of Life and overall results. Poster presentation ASCO May 30-June 2, 2014, Chicago Illinois.
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Public notes
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Contacts
Principal investigator
Name
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Dr Kumar Gogna
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Address
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Queensland Radium Institute-Mater Centre
Raymond Terrace
South Brisbane, Queensland, 4101, Australia
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Country
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Australia
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Phone
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+61 7 3840 3255
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Kacy Baumann
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Address
10490
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Mater QRI
Raymond Terrace
South Brisbane QLD 4101
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Country
10490
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Australia
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Phone
10490
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+61 7 3840 3219
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Fax
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Email
10490
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[email protected]
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Contact person for scientific queries
Name
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Kumar Gogna
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Address
1418
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Mater QRI
Raymond Terrace
SOUTH BRISBANE QLD 4101
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Country
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Australia
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Phone
1418
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+61 7 3840 3255
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF