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NCT02582697PHASE3Recruiting

Accelerated v's Standard BEP Chemotherapy for Patients With Intermediate and Poor-risk Metastatic Germ Cell Tumours

University of Sydney

Start Date

2/1/2014

Completion Date

12/31/2029

Summary

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.

Detailed Description

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.

Eligibility Criteria

Age Range: 11 years to 50 years

Inclusion Criteria: 1. Age ≥ 11 years and ≤ 50 years on the date of randomisation 2. Histologically or cytologically confirmed germ cell tumour (non-seminoma or seminoma); or Exceptionally raised tumour markers (AFP ≥ 1000ng/mL and/or HCG ≥ 5000 IU/L) without histologic or cytologic confirmation in the rare case where pattern of metastases consistent with GCT, high tumour burden, and a need to start therapy urgently 3. Primary arising in testis, ovary, retro-peritoneum, or mediastinum 4. Metastatic disease or non-testicular primary 5. Intermediate or poor prognosis as defined by IGCCC classification3 (modified with different LDH criteria for intermediate risk non-seminoma, and inclusion of ovarian primaries). (See protocol for more information). 6. Adequate bone marrow function with ANC ≥1.0 x 10\^9/L, Platelet count ≥100 x 10\^9/L 7. Adequate liver function where bilirubin must be ≤1.5 x ULN, except participants with Gilbert's Syndrome where bilirubin must be ≤2.0 x ULN; ALT and AST must be ≤2.5 x ULN, except if the elevations are due to hepatic metastases, in which case ALT and AST must be ≤ 5 x ULN 8. Adequate renal function with estimated creatinine clearance of ≥60 ml/min according to the Cockcroft-Gault formula, unless calculated to be \< 60 ml/min or borderline in which case GFR should be formally measured, eg. with EDTA scan 9. ECOG Performance Status of 0, 1, 2, or 3 10. Study treatment both planned and able to start within 14 days of randomisation. 11. Willing and able to comply with all study requirements, including treatment, timing and nature of required assessments 12. Able to provide signed, written informed consent Exclusion Criteria: 1. Other primary malignancy (EXCEPT adequately treated non-melanomatous carcinoma of the skin, germ cell tumour, or other malignancy treated at least 5 years previously with no evidence of recurrence) 2. Previous chemotherapy or radiotherapy, except if patient has pure seminoma relapsing after adjuvant radiotherapy or adjuvant chemotherapy with 1-2 doses of single agent carboplatin or if patient hasb. non-seminoma by IGCCC criteria or stage IV malignant ovarian germ cell tumour in the rare case where low-dose induction chemotherapy is given prior to registration because patient is not fit enough to receive protocol chemotherapy (eg. organ failure, vena cava obstruction, overwhelming burden of disease). Acceptable regimens include cisplatin 20 mg/m2 days 1-2 and etoposide 100 mg/m2 days 1-2; carboplatin AUC 3 days 1-2 and etoposide 100 mg/m2 days 1-2; or baby-BOP.43 Patients must meet all other inclusion and exclusion criteria at the time of registration. Additionally participants who need to start therapy urgently prior to completing study-specific baseline investigations may commence study chemotherapy prior to registration and randomisation. Such patients must be discussed with the coordinating centre prior to registration, and must be registered within 10 days of commencing study chemotherapy. 3. Significant cardiac disease resulting in inability to tolerate IV fluid hydration for cisplatin 4. Significant co-morbid respiratory disease that contraindicates the use of bleomycin 5. Peripheral neuropathy ≥ grade 2 or clinically significant sensorineural hearing loss or tinnitus 6. Concurrent illness, including severe infection that may jeopardize the ability of the participant to undergo the procedures outlined in this protocol with reasonable safety 7. Inadequate contraception. Men must use 2 effective methods of contraception, including use of a condom, during chemotherapy and for a year after completing chemotherapy. 8. Known allergy or hypersensitivity to any of the study drugs 9. Presence of any psychological, familial, sociological or geographical condition that in the opinion of the investigator would hamper compliance with the study protocol and follow-up schedule, including alcohol dependence or drug abuse The above inclusion and exclusion criteria will apply to stage 1 (n=150) and stage 2 (n=500 including stage 1) of the study. All sites will participate in both stages of the study with the exception of the Children's Oncology Group who will be participate in stage 1 only.

Interventions

DRUG

Bleomycin (active name: Bleomycin Sulfate)

DRUG

Etoposide

DRUG

Cisplatin

DRUG

Pegylated G-CSF (Pegfilgrastim)

DRUG

Filgrastim

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Conditions

Germ Cell Tumor

Locations

Memorial Sloan Kettering Cancer Centre

New York, New York 10065

United States

Calvary Mater Newcastle

Newcastle, New South Wales 2298

Australia

Royal North Shore Hospital

St Leonards, New South Wales 2065

Australia

Prince of Wales Hospital

Sydney, New South Wales 2031

Australia

Chris O'Brien Lifehouse

Sydney, New South Wales 2050

Australia

Macquarie Cancer Clinical Trials

Sydney, New South Wales 2109

Australia

Concord Repatriation General Hospital

Sydney, New South Wales 2139

Australia

Westmead Hospital

Sydney, New South Wales 2145

Australia

Nepean Hospital

Sydney, New South Wales 2751

Australia

Tweed Hospital

Tweed Heads, New South Wales 2485

Australia

SAN Clinical Trials Unit

Wahroonga, New South Wales 2076

Australia

Royal Brisbane & Women's Hospital

Brisbane, Queensland 4029

Australia

Queensland Children's Hospital

South Brisbane, Queensland 4101

Australia

Princess Alexandra

Woolloongabba, Queensland 4102

Australia

Royal Adelaide Hospital

Adelaide, South Australia 5000

Australia

Flinders Medical Centre

Bedford Park, South Australia 5042

Australia

Royal Hobart Hospital

Hobart, Tasmania 7000

Australia

Box Hill Hospital

Box Hill, Victoria 3128

Australia

Peter MacCallum Cancer Centre

East Melbourne, Victoria 3002

Australia

Austin Health

Heidelberg, Victoria 3084

Australia

Sunshine Hospital

St Albans, Victoria 3021

Australia

Border Medical Oncology

Wodonga, Victoria 3690

Australia

Fiona Stanley Hospital

Murdoch, Western Australia 6847

Australia

Starship Children's Hospital

Grafton, Auckland 1023

New Zealand

Auckland Hospital

Grafton, Auckland 1142

New Zealand

Palmerston North Hospital

Roslyn, Palmerston North 4442

New Zealand

Christchurch Hospital

Christchurch, 8011

New Zealand

Dunedin Hospital

Dunedin, 9054

New Zealand