EFFECTIVE CHEMOTHERAPY FOR ADVANCED CNS EMBRYONAL TUMORS IN ADULTS

Citation
E. Galanis et al., EFFECTIVE CHEMOTHERAPY FOR ADVANCED CNS EMBRYONAL TUMORS IN ADULTS, Journal of clinical oncology, 15(8), 1997, pp. 2939-2944
Citations number
26
Categorie Soggetti
Oncology
ISSN journal
0732183X
Volume
15
Issue
8
Year of publication
1997
Pages
2939 - 2944
Database
ISI
SICI code
0732-183X(1997)15:8<2939:ECFACE>2.0.ZU;2-K
Abstract
Purpose: Embryonal tumors of the CNS include, among others, medullobla stoma, cerebral neuroblastoma, pineoblastoma, and primitive neuroectod ermal tumors (PNETs). Almost all data on the treatment of embryonal CN S tumors are derived from the pediatric population, since these tumors are uncommon in adulthood. The purpose of this study was to examine t he rate and duration of response to chemotherapy of advanced embryonal CNS tumors in adults. Patients and Method's: We retrospectively studi ed all adult (> 18 years of age) patients with advanced embryonal tumo rs of the CNS who received chemotherapy at our institution between 197 6 and 1994. Seventeen consecutive patients were treated with regimens that contained either nitrosourea or cisplatin or both sequentially, w ith no patients having received the combination of nitrosourea and cis platin concurrently. Results: In patients who received cisplatin-based chemotherapy, responses were observed in 84.5% (26% complete response [CR] rate), 10.5% remained stable, and 5% progressed, The median time to progression was 18 months for patients who had a CR, 6 months for those with partial response (PR), and 10 months for stable patients. A mong patients who received nitrosourea-based chemotherapy, PR was obse rved in 27%, 36.5% remained stable, and 36.5% progress. The median tim e to progression was 6 months for patients who had a PR and 6.5 months far stable patients. Conclusion: in adults with advanced embryonal CN S tumors, conventional-dose intravenous cisplatin-based chemotherapy r egimens are able to produce responses in the majority of the patients (84.5%), even as second- or third-line regimens. Nitrosourea-based reg imens less frequently produce responses (27%). (C) 1997 by American So ciety of Clinical Oncology.