The purpose of this study is to determine whether accelerated BEP chemotherapy is more effective than standard BEP chemotherapy in males with intermediate and poor-risk metastatic germ cell tumours.
Bleomycin, Etoposide, Cisplatin (BEP) administered 3-weekly x 4 remains standard 1st line chemotherapy for intermediate- and poor-risk metastatic germ cell tumours (GCTs). Cure rates are over 90% for good-risk disease, 85% with intermediate-risk, and about 70% for poor-risk disease. Previous strategies to improve first-line chemotherapy have failed to improve cure rates and were more toxic than BEP. New strategies are needed for patients with intermediate and poor-risk disease. BEP is accelerated by cycling Cisplatin and etoposide 2-weekly instead of 3-weekly. The Australian and New Zealand Urogenital and Prostate Cancer Trials Group (ANZUP) is conducting a trial comparing accelerated BEP with standard BEP. The aim of this study is to determine if accelerated BEP is superior to standard BEP as first-line chemotherapy for intermediate and poor risk metastatic GCTs.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
500
Standard Arm: Bleomycin 30,000 international units IV weekly for 3 doses (eg. days 1, 8 and 15 or days 2, 9 and 16 of a 21-day cycle) for 4 cycles. Accelerated Arm: Bleomycin 30,000 international units IV weekly for 2 doses (eg. days 1 and 8 or days 2 and 9 of a 14-day cycle) for 4 cycles. Followed by Bleomycin 30,000 international units IV weekly for 4 doses.
Standard Arm: Etoposide 100 mg/m2 IV on days 1, 2, 3, 4, 5 of a 21-day cycle for 4 cycles. Accelerated Arm: 100 mg/m2 IV on days 1, 2, 3, 4, 5 of a 14-day cycle for 4 cycles.
Standard Arm: Cisplatin 20 mg/m2 IV on days 1, 2, 3, 4, 5 of a 21-day cycle for 4 cycles. Accelerated Arm: Cisplatin 20 mg/m2 IV on days 1, 2, 3, 4, 5 of a 14-day cycle for 4 cycles.
Progression-free survival (disease progression or death)
PFS is measured from the date of randomisation until the criteria for disease progression are met (as defined in the protocol) or death. Participants who are not observed to progress nor die will be censored at the date of last follow-up
Time frame: From randomisation up to disease progression or date of death whichever come first, assessed up to 5 years
Initial response assessment
The assessment of response of germ cell tumours is measured by the change in size of measurable tumour masses in combination with changes in serum tumour markers after chemotherapy treatment.
Time frame: At end of chemotherapy treatment, treatment planned for 12 weeks
Final response assessment
The assessment of response of germ cell tumours is measured by changes in serum tumour markers and imaging at 6 months from randomisation, or after any post-chemotherapy surgical resection or other intervention, whichever occurs last.
Time frame: At 6 months
Adverse events (worst grade according to NCI CTCAE v4.03)
The intensity of adverse events will be assessed using the NCI Common Terminology Criteria for Adverse Events version 4 (NCI CTCAE v4.03)
Time frame: From start of chemotherapy until 30 days after last dose, an average of 4 months
Health-related quality of life
HR-QoL measures will include the EORTC core quality of life questionnaire (QLQ-C30), a 30-item cancer-specific questionnaire that is well-validated and available in many languages.
Time frame: From date of randomisation until date of 18 month follow-up
Health-related quality of life for testicular cancer
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Standard Arm: 6 mg SCI on day 6 of a 21-day cycle for 4 cycles. Accelerated Arm: 6 mg SCI on day 6 of a 14-day cycle for 4 cycles.
Standard Arm: 10 mcg/kg/day on day6, until post-nadir absolute neutrophil count ≥ 1.0 x 10\^9/L, of a 21-day cycle for 4 cycles. Accelerated Arm: 10 mcg/kg/day on day 6, until post-nadir absolute neutrophil count ≥ 1.0 x 10\^9/L, of a 14-day cycle for 4 cycles.
Memorial Sloan Kettering Cancer Centre
New York, New York, United States
RECRUITINGCalvary Mater Newcastle
Newcastle, New South Wales, Australia
RECRUITINGRoyal North Shore Hospital
St Leonards, New South Wales, Australia
RECRUITINGPrince of Wales Hospital
Sydney, New South Wales, Australia
RECRUITINGChris O'Brien Lifehouse
Sydney, New South Wales, Australia
RECRUITINGMacquarie Cancer Clinical Trials
Sydney, New South Wales, Australia
RECRUITINGConcord Repatriation General Hospital
Sydney, New South Wales, Australia
RECRUITINGWestmead Hospital
Sydney, New South Wales, Australia
WITHDRAWNNepean Hospital
Sydney, New South Wales, Australia
RECRUITINGTweed Hospital
Tweed Heads, New South Wales, Australia
RECRUITING...and 18 more locations
EORTC quality of life module for testicular cancer (QLQ-TC26), a disease-specific measure with 26 items about physical symptoms, sexual functioning and emotional issues.
Time frame: From date of randomisation until date of 18 month follow-up
Treatment preference
A trial-specific preferences question will be used to determine if participants think they would prefer to be treated with accelerated BEP or standard BEP, assuming that they were equally effective.
Time frame: From date of randomisation until date of 18 month follow-up
Delivered dose-intensity of chemotherapy (relative to standard BEP)
Delivered dose-intensity of cisplatin, etoposide and bleomycin will be assessed.
Time frame: From start date of chemotherapy treatment until date of end of chemotherapy, an average of 12 weeks
Overall survival
Overall survival is measured from the date of randomisation until death from any cause, or the date of last known follow-up alive.
Time frame: From randomisation up to disease progression or date of death whichever come first, assessed up to 5 years