A. Flechon et al., High-dose chemotherapy with hematopoietic stem-cell support in germ-cell tumor patient treatment: The French experience, INT J CANC, 83(6), 1999, pp. 844-847
Germ-cell tumors (GCTs) are very chemosensitive and highly curable cancers.
For the small proportion of patients who fail conventional chemotherapy (C
T), high-dose CT (HDCT) was introduced in France and elsewhere in 1982-1984
. We report here on the French experience with HDCT in GCTs. At the Centre
Leon Berard, 75 patients were treated with HDCT between 1982 and 1996. Pati
ents received HDCT in 2 different settings: 46 in consolidation of first-li
ne treatment or in incomplete response, 29 in salvage of relapse or refract
ory disease. The most common regimens of HDCT were the combination of etopo
side, double-dose cisplatin and either ifosfamide (VIC regimen, n = 46) or
cyclophosphamide (PEC regimen, n = 9) and the combination of carboplatin, e
toposide and cyclophosphamide (Carbo-PEC regimen, n = 17), Seven patients d
ied of toxicity. The median follow-up was 42 months. Forty-five of 75 patie
nts are alive and free of disease at long term, 2 of whom had refractory di
sease. The median time to recovery of a granulocyte count greater than or e
qual to 0.5 x 10(9)/1 and a platelet count greater than or equal to 25 x 10
(9)/1 was 14 and II days, respectively. The French development was based on
double-dose cisplatin until the results of the French randomized trial, wh
ich showed no advantage of HDCT in the first-line treatment of poor-risk gr
oup patients. Then carboplatin was associated with etoposide and cyclophosp
hamide in a phase I trial. A European randomized trial, which studies the r
ole of HDCT in the first-line salvage treatment of non-refractory disease,
is ongoing. So far, HDCT is not a standard treatment of GCT. (C) 1999 Wiley
-Liss, Inc.