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The role of high-dose chemotherapy in the management of germ cell tumors

Bastos, Diogo A.a; Feldman, Darren R.b,c

doi: 10.1097/CCO.0000000000000070
GENITOURINARY SYSTEM: Edited by Arif Hussain

Purpose of review To discuss the current role and future perspectives of high-dose chemotherapy (HDCT) in the management of advanced germ cell tumors (GCTs).

Recent findings Multiple studies have demonstrated the safety and efficacy of HDCT, consisting of carboplatin and etoposide followed by stem cell reinfusion, for the salvage treatment of GCTs. However, three randomized trials showed no benefit for HDCT over conventional dose chemotherapy in the first-line setting. Similarly, adding a third drug to etoposide with carboplatin does not seem to substantially improve treatment efficacy and may increase toxicity and mortality. Recent retrospective data from single centers and a large international collaboration demonstrated better outcomes with use of HDCT in the initial (rather than later) salvage setting as well as with sequential rather than single cycle regimens. However, randomized data are lacking. Prognostic factors for outcome to salvage HDCT were recently established and enhanced supportive measures such as growth factors and antibiotic prophylaxis have resulted in a dramatic decrease in morbidity and mortality.

Summary HDCT plays an integral role in the salvage treatment of patients with advanced GCTs. However, optimal timing (initial vs. later salvage), dosing, number of high-dose cycles, and patient selection remain to be defined.

aGenitourinary Oncology, Oncology Center, Hospital Sirio-Libanes, Sao Paulo, Brazil

bGenitourinary Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center

cDepartment of Medicine, Weill Medical College of Cornell University, New York, New York, USA

Correspondence to Darren R. Feldman, MD, Genitourinary Oncology Service, Memorial Sloan-Kettering Cancer Center, 353 East 68th street, New York, NY 10065, USA. Tel: +1 646 422 4491; fax: +1 212 988 0701; e-mail:

© 2014 Lippincott Williams & Wilkins, Inc.