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Erschienen in: Journal of Neuro-Oncology 2/2016

03.03.2016 | Clinical Study

Adjuvant chemotherapy in adult medulloblastoma: is it an option for average-risk patients?

verfasst von: E. Franceschi, M. Bartolotti, A. Paccapelo, G. Marucci, R. Agati, L. Volpin, D. Danieli, C. Ghimenton, M. P. Gardiman, C. Sturiale, R. Poggi, M. Mascarin, D. Balestrini, B. Masotto, A. A. Brandes

Erschienen in: Journal of Neuro-Oncology | Ausgabe 2/2016

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Abstract

The standard treatment in children with average-risk medulloblastoma (MB) is reduced-dose radiotherapy (RT) followed by chemotherapy. However, in adults, there is no agreement on the use of adjuvant chemotherapy. We performed a retrospective analysis of adult MB patients with average-risk disease, defined as no postsurgical residual (or ≤1.5 cm2) and no metastatic disease (M0). Main inclusion criteria were: age >16 years, post-surgical treatment with craniospinal irradiation with or without adjuvant chemotherapy (cisplatin and etoposide ± cyclophosphamide). From 1988 to 2012 were accrued 43 average-risk MB patients treated with surgery and adjuvant RT. Fifteen (34.9 %) patients received also chemotherapy: 7 before RT, 5 after RT, and 3 before and after RT. Reasons to administer chemotherapy were presence of residual disease (even if ≤1.5 cm) and delay in RT. After a median follow up time of 10 years (range: 8–13), median survival was 18 years (95 % CI 9–28) in patients who receive RT alone, and was not reached in patients treated with RT plus chemotherapy. The survival rates at 5, 10 and 15 years were 100 %, 78.6 % (95 % CI 60.0–97.2 %) and 60.2 % (95 % CI 36.9–83.5 %), in patients treated with RT alone, and 100, 100 and 100 %, in patients treated with RT plus chemotherapy (p = 0.079). Our findings suggest a role for adjuvant chemotherapy in the treatment of average-risk MB adult patients. Further improvements might drive to add chemotherapy in average-risk setting with less favourable biological signatures (i.e., non-WNT group).
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Metadaten
Titel
Adjuvant chemotherapy in adult medulloblastoma: is it an option for average-risk patients?
verfasst von
E. Franceschi
M. Bartolotti
A. Paccapelo
G. Marucci
R. Agati
L. Volpin
D. Danieli
C. Ghimenton
M. P. Gardiman
C. Sturiale
R. Poggi
M. Mascarin
D. Balestrini
B. Masotto
A. A. Brandes
Publikationsdatum
03.03.2016
Verlag
Springer US
Erschienen in
Journal of Neuro-Oncology / Ausgabe 2/2016
Print ISSN: 0167-594X
Elektronische ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-016-2097-x

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