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Relapse in medulloblastoma: what can be done after abandoning high-dose chemotherapy? A mono-institutional experience.

Authors :
Massimino, Maura
Casanova, Michela
Polastri, Daniela
Biassoni, Veronica
Modena, Piergiorgio
Pecori, Emilia
Schiavello, Elisabetta
Pava, Marco
Indini, Alice
Rampini, Paolo
Bauer, Dario
Catania, Serena
Podda, Marta
Gandola, Lorenza
Source :
Child's Nervous System. Jul2013, Vol. 29 Issue 7, p1107-1112. 6p.
Publication Year :
2013

Abstract

Purpose: We retrospectively report strategies used for medulloblastoma patients progressing after craniospinal irradiation where we aimed for: symptom control, a satisfactory quality of life, accrual in phase 1-2 trials, when available, and the first two conditions could no longer be satisfied by already experienced second-line strategies. Methods: Surgery was used in cases of doubtful relapse or when only one site was affected. Radiotherapy was given whenever possible, especially to relieve symptoms. The main chemotherapy regimens were oral temozolomide/etoposide, intravenous (iv.) cisplatin/etoposide, iv. gemcitabine/oxaliplatin, an oral sonic hedgehog pathway inhibitor and oral melphalan. Results: Between 1998 and 2011, we treated 18 patients relapsed after median 20 months. Nine had relapsed locally, four had dissemination, three single metastases, and two had one synchronous local and metastatic recurrence. Responses to chemotherapy were seen in 32 % of cases. The median hospital stay for treatments/complications was 19 days. The 1- and 3-year progression-free survival (PFS) rates were 28 ± 10 % and 0 %, respectively, for OS, they were 44 ± 12 % and 22 ± 10 % but no patient was cured. The median PFS after a first relapse was 7 months (range 1-29); the median OS was 7 months (range 4-44). No patients died due to treatment toxicity. Late recurrence (more than 1-2 years after diagnosis) and involvement of single sites were favorable prognostic factors. Conclusions: Without succeeding in patients cure, we ensured them further treatment with short hospital stay thus affording low personal and social costs. The chances of cure may emerge from tailored therapies according to genetic stratification. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02567040
Volume :
29
Issue :
7
Database :
Academic Search Index
Journal :
Child's Nervous System
Publication Type :
Academic Journal
Accession number :
88155169
Full Text :
https://doi.org/10.1007/s00381-013-2104-x