Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: Accelerated BEP for metastatic germ cell tumours: a multicenter phase II trial by the Australian and New Zealand Urogenital and Prostate Cancer Trials Group (ANZUP)
Author: Grimison, P.
Stockler, M.
Chatfield, M.
Thomson, D.
Gebski, V.
Friedlander, M.
Boland, A.
Houghton, B.
Gurney, H.
Rosenthal, M.
Singhal, N.
Kichenadasse, G.
Wong, S.
Lewis, C.
Vasey, P.
Toner, G.
Australian and New Zealand Urogenital and Prostate Cancer Trials Group,
Citation: Annals of Oncology, 2014; 25(1):143-148
Publisher: Oxford University Press
Issue Date: 2014
ISSN: 0923-7534
Statement of
P. S. Grimison, M. R. Stockler, M. Chatfield, D. B. Thomson, V. Gebski, M. Friedlander, A. L. Boland, B. Houghton, H. Gurney, M. Rosenthal, N. Singhal, G. Kichenadasse, S. S. Wong, C. R. Lewis, P. A. Vasey and G. C. Toner Australian and New Zealand Urogenital and Prostate Cancer Trials Group
Abstract: Background: This Australian single-arm, multicenter, phase II trial evaluated feasibility, tolerability and activity of accelerated bleomycin, etoposide and cisplatin (BEP) as first-line chemotherapy for metastatic germ cell tumours. Patients and methods: Patients were planned to receive cisplatin 20 mg/m(2) and etoposide 100 mg/m(2) days 1-5, and pegfilgrastim 6 mg day 6, all repeated every 2 weeks for four cycles (three cycles for good prognosis). Bleomycin was given at 30 000 IU weekly to a total of 12 doses (9 doses for good prognosis). Primary end point was feasibility, defined as the proportion of patients able to complete the etoposide and cisplatin components of BEP and be eligible to receive a fourth cycle of BEP by day 50. Results: Twelve poor, 16 intermediate and 15 good prognosis (n = 43) eligible patients were enrolled. Two patients aged >40 years were ineligible and excluded from analyses. The regimen was feasible in 86%, not feasible in 7% and not assessable in 7% of patients. Most common grade 3/4 adverse events were non-neutropenic infection (16%) and febrile neutropenia (12%). Complete response (CR) to chemotherapy and surgery was achieved in 33% poor-prognosis, 81% intermediate-prognosis and 100% good-prognosis patients. At median follow-up of 27 months (range 6-42), the 2-year progression-free survival was 50% for poor-prognosis, 94% for intermediate-prognosis and 92% for good-prognosis patients. Conclusion: Accelerated BEP is feasible and tolerable. Efficacy data appear to be promising. This trial and a similar UK study provide the rationale for a randomised trial comparing accelerated versus standard BEP. Australian New Zealand Clinical Trials Registry Registration number. ACTRN 12607000294459.
Keywords: Accelerated; antineoplastic combined chemotherapy; growth factors; germ cell tumours; testicular neoplasms; dose-density
Rights: © The Author 2013. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved.
DOI: 10.1093/annonc/mdt369
Published version:
Appears in Collections:Aurora harvest 8
Medicine publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.