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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).
Literatur
1.
Zurück zum Zitat Smoll NR, Drummond KJ (2012) The incidence of medulloblastomas and primitive neurectodermal tumours in adults and children. J Clin Neurosci 19:1541–1544CrossRefPubMed Smoll NR, Drummond KJ (2012) The incidence of medulloblastomas and primitive neurectodermal tumours in adults and children. J Clin Neurosci 19:1541–1544CrossRefPubMed
2.
Zurück zum Zitat Brandes AA, Franceschi E, Tosoni A et al (2007) Long-term results of a prospective study on the treatment of medulloblastoma in adults. Cancer 110:2035–2041CrossRefPubMed Brandes AA, Franceschi E, Tosoni A et al (2007) Long-term results of a prospective study on the treatment of medulloblastoma in adults. Cancer 110:2035–2041CrossRefPubMed
3.
Zurück zum Zitat Padovani L, Sunyach MP, Perol D et al (2007) Common strategy for adult and pediatric medulloblastoma: a multicenter series of 253 adults. Int J Radiat Oncol Biol Phys 68:433–440CrossRefPubMed Padovani L, Sunyach MP, Perol D et al (2007) Common strategy for adult and pediatric medulloblastoma: a multicenter series of 253 adults. Int J Radiat Oncol Biol Phys 68:433–440CrossRefPubMed
4.
Zurück zum Zitat Chang CH, Housepian EM, Herbert C Jr (1969) An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas. Radiology 93:1351–1359CrossRefPubMed Chang CH, Housepian EM, Herbert C Jr (1969) An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas. Radiology 93:1351–1359CrossRefPubMed
5.
Zurück zum Zitat Packer RJ, Goldwein J, Nicholson HS et al (1999) Treatment of children with medulloblastomas with reduced-dose craniospinal radiation therapy and adjuvant chemotherapy: a Children’s Cancer Group Study. J Clin Oncol 17:2127–2136PubMed Packer RJ, Goldwein J, Nicholson HS et al (1999) Treatment of children with medulloblastomas with reduced-dose craniospinal radiation therapy and adjuvant chemotherapy: a Children’s Cancer Group Study. J Clin Oncol 17:2127–2136PubMed
6.
Zurück zum Zitat Packer RJ, Gajjar A, Vezina G et al (2006) Phase III study of craniospinal radiation therapy followed by adjuvant chemotherapy for newly diagnosed average-risk medulloblastoma. J Clin Oncol 24:4202–4208CrossRefPubMed Packer RJ, Gajjar A, Vezina G et al (2006) Phase III study of craniospinal radiation therapy followed by adjuvant chemotherapy for newly diagnosed average-risk medulloblastoma. J Clin Oncol 24:4202–4208CrossRefPubMed
7.
Zurück zum Zitat Brandes AA, Ermani M, Amista P et al (2003) The treatment of adults with medulloblastoma: a prospective study. Int J Radiat Oncol Biol Phys 57:755–761CrossRefPubMed Brandes AA, Ermani M, Amista P et al (2003) The treatment of adults with medulloblastoma: a prospective study. Int J Radiat Oncol Biol Phys 57:755–761CrossRefPubMed
8.
Zurück zum Zitat Brandes AA, Pasetto LM, Lumachi F et al (2000) Endocrine dysfunctions in patients treated for brain tumors: incidence and guidelines for management. J Neurooncol 47:85–92CrossRefPubMed Brandes AA, Pasetto LM, Lumachi F et al (2000) Endocrine dysfunctions in patients treated for brain tumors: incidence and guidelines for management. J Neurooncol 47:85–92CrossRefPubMed
9.
Zurück zum Zitat Brown AP, Barney CL, Grosshans DR et al (2013) Proton beam craniospinal irradiation reduces acute toxicity for adults with medulloblastoma. Int J Radiat Oncol Biol Phys 86(2):277–284CrossRefPubMedPubMedCentral Brown AP, Barney CL, Grosshans DR et al (2013) Proton beam craniospinal irradiation reduces acute toxicity for adults with medulloblastoma. Int J Radiat Oncol Biol Phys 86(2):277–284CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Friedrich C, von Bueren AO, von Hoff K et al (2013) Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study. Eur J Cancer 49:893–903CrossRefPubMed Friedrich C, von Bueren AO, von Hoff K et al (2013) Treatment of adult nonmetastatic medulloblastoma patients according to the paediatric HIT 2000 protocol: a prospective observational multicentre study. Eur J Cancer 49:893–903CrossRefPubMed
11.
Zurück zum Zitat Kortmann RD, Kuhl J, Timmermann B et al (2000) Postoperative neoadjuvant chemotherapy before radiotherapy as compared to immediate radiotherapy followed by maintenance chemotherapy in the treatment of medulloblastoma in childhood: results of the German prospective randomized trial HIT ‘91. Int J Radiat Oncol Biol Phys 46:269–279CrossRefPubMed Kortmann RD, Kuhl J, Timmermann B et al (2000) Postoperative neoadjuvant chemotherapy before radiotherapy as compared to immediate radiotherapy followed by maintenance chemotherapy in the treatment of medulloblastoma in childhood: results of the German prospective randomized trial HIT ‘91. Int J Radiat Oncol Biol Phys 46:269–279CrossRefPubMed
12.
Zurück zum Zitat Tarbell NJ, Friedman H, Polkinghorn WR et al (2013) High-risk medulloblastoma: a pediatric oncology group randomized trial of chemotherapy before or after radiation therapy (POG 9031). J Clin Oncol 31:2936–2941CrossRefPubMedPubMedCentral Tarbell NJ, Friedman H, Polkinghorn WR et al (2013) High-risk medulloblastoma: a pediatric oncology group randomized trial of chemotherapy before or after radiation therapy (POG 9031). J Clin Oncol 31:2936–2941CrossRefPubMedPubMedCentral
13.
Zurück zum Zitat Gajjar A, Stewart CF, Ellison DW et al (2013) Phase I study of vismodegib in children with recurrent or refractory medulloblastoma: a pediatric brain tumor consortium study. Clin Cancer Res 19:6305–6312CrossRefPubMed Gajjar A, Stewart CF, Ellison DW et al (2013) Phase I study of vismodegib in children with recurrent or refractory medulloblastoma: a pediatric brain tumor consortium study. Clin Cancer Res 19:6305–6312CrossRefPubMed
14.
Zurück zum Zitat Rodon J, Tawbi HA, Thomas AL et al (2014) A phase 1, multicenter, open-label, first-in-human, dose-escalation study of the oral hedgehog inhibitor Sonidegib (LDE225) in patients with advanced solid tumors. Clin Cancer Res 20:1900CrossRefPubMed Rodon J, Tawbi HA, Thomas AL et al (2014) A phase 1, multicenter, open-label, first-in-human, dose-escalation study of the oral hedgehog inhibitor Sonidegib (LDE225) in patients with advanced solid tumors. Clin Cancer Res 20:1900CrossRefPubMed
15.
Zurück zum Zitat Brandes AA, Franceschi E (2014) Shedding light on adult medulloblastoma: current management and opportunities for advances. Am Soc Clin Oncol Educ Book 34:e82-7CrossRef Brandes AA, Franceschi E (2014) Shedding light on adult medulloblastoma: current management and opportunities for advances. Am Soc Clin Oncol Educ Book 34:e82-7CrossRef
16.
Zurück zum Zitat Brandes AA, Franceschi E (2010) Neuro-oncology: genetic variation in pediatric and adult brain tumors. Nat Rev Neurol 6(12):653–654CrossRefPubMed Brandes AA, Franceschi E (2010) Neuro-oncology: genetic variation in pediatric and adult brain tumors. Nat Rev Neurol 6(12):653–654CrossRefPubMed
17.
Zurück zum Zitat Brandes AA, Franceschi E, Tosoni A et al (2009) Adult neuroectodermal tumors of posterior fossa (medulloblastoma) and of supratentorial sites (stPNET). Crit Rev Oncol Hematol 71(2):165–179CrossRefPubMed Brandes AA, Franceschi E, Tosoni A et al (2009) Adult neuroectodermal tumors of posterior fossa (medulloblastoma) and of supratentorial sites (stPNET). Crit Rev Oncol Hematol 71(2):165–179CrossRefPubMed
18.
Zurück zum Zitat Brandes AA, Paris MK (2004) Review of the prognostic factors in medulloblastoma of children and adults. Crit Rev Oncol Hematol 50(2):121–128CrossRefPubMed Brandes AA, Paris MK (2004) Review of the prognostic factors in medulloblastoma of children and adults. Crit Rev Oncol Hematol 50(2):121–128CrossRefPubMed
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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