Volume 14, Issue 4 pp. 336-338
Original Article: Clinical Investigation

First-line high-dose chemotherapy combined with peripheral blood stem cell transplantation for patients with advanced extragonadal germ cell tumors

Masafumi Kumano

Masafumi Kumano

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan

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Hideaki Miyake

Hideaki Miyake

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan

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Isao Hara

Isao Hara

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan

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Junya Furukawa

Junya Furukawa

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan

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Atsushi Takenaka

Atsushi Takenaka

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan

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Masato Fujisawa

Masato Fujisawa

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan

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First published: 26 April 2007
Citations: 7
Hideaki Miyake md, Division of Urology, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan. Email: [email protected]

Abstract

Background:  The objective of this study was to evaluate the efficacy and safety of first-line high-dose chemotherapy (HDCT) combined with peripheral blood stem cell transplantation (PBSCT) for patients with advanced extragonadal germ cell tumors (EGGCT).

Methods:  Six male patients with advanced non-seminomatous EGGCT were treated with HDCT combined with PBSCT following 2–3 cycles of conventional-dose induction chemotherapy. The regimens used for HDCT were carboplatin, etoposide and ifosfamide (ICE) in five patients and ICE plus paclitaxel (T-ICE) in one patient, and that for induction therapy was cisplatin, etoposide and bleomycin (PEB) in all patients. As a rule, HDCT was continuously administered until α-fetoprotein (AFP) and β-human chorionic gonadotropin normalized (β-HCG).

Results:  Following 1–6 courses of HDCT (median, 4 courses), β-HCG and AFP were normalized in all patients, and five and one patient were diagnosed as showing partial remission and stable disease, respectively. Five patients underwent surgical resection of residual tumors after HDCT, yielding necrotic tissue in two, mature teratoma in two, and viable cancer tissue in one, and the surgical margin was negative in all patients. At a median follow-up of 36 months, five patients were alive and disease-free, whereas the remaining one died of disease progression. Although all patients had grade 3 hematological toxicity, there was no treatment-related death by combining PBSCT.

Conclusions:  First-line HDCT with PBSCT could be safely administered to patients with advanced EGGCT, and the antitumor effect of this treatment was comparatively favorable. First-line HDCT therefore may represent an attractive option for patients with advanced EGGCT.

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