Literature DB >> 16942675

Current therapy for medulloblastoma.

Nicholas G Gottardo1, Amar Gajjar.   

Abstract

In the past three decades, the survival for patients with medulloblastoma has improved remarkably. Contemporary "standard" therapy for children with medulloblastoma consists of maximal surgical resection followed by craniospinal irradiation with a boost to the posterior fossa, combined with adjuvant chemotherapy. The use of such multimodal therapeutic approaches results in progression-free survival (PFS) rates of 75% to 80% for patients with average-risk disease and approximately 60% for high-risk patients. However, despite the marked improvements in survival, many therapeutic challenges remain. Children with macroscopic metastatic disease (M2/M3) at presentation continue to fare poorly, with the best reports only attaining PFS rates up to 40%. Furthermore, despite intensive multimodal therapy, some patients have disease progression or recurrence, which for most remains incurable. The early recognition of these patients is imperative in order to institute treatment modifications, such as intensification and/or the use of novel experimental therapies. Additionally, the price for cure is clearly evident in survivors, who suffer from significant, often debilitating long-term neurocognitive and neuroendocrine sequela. Using the current clinical stratification system, a significant number of patients are overtreated and unnecessarily subjected to these long-term toxicities. This group of patients would benefit from reductions in therapy. Refinements in patient stratification and further improvement in outcome are unlikely to be achieved without improved knowledge of tumor biology. Several molecular alterations have already been identified, many of which appear to have prognostic significance. Furthermore, the disruption of molecular alterations in signaling pathways involved in the development and maintenance of medulloblastoma using novel molecularly targeted therapies promises to improve outcomes and reduce toxicity for patients with medulloblastoma. It is envisaged that in the near future children diagnosed with medulloblastoma will be more accurately stratified based on a combination of clinical variables and molecular profiles. Improved risk stratification will permit delivery of individualized therapy using conventional treatment modalities in conjunction with novel targeted therapeutic approaches.

Entities:  

Year:  2006        PMID: 16942675     DOI: 10.1007/s11940-006-0022-x

Source DB:  PubMed          Journal:  Curr Treat Options Neurol        ISSN: 1092-8480            Impact factor:   3.972


  52 in total

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Authors:  David W Ellison; Steven C Clifford; Amar Gajjar; Richard J Gilbertson
Journal:  Eur J Paediatr Neurol       Date:  2003       Impact factor: 3.140

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Journal:  Nature       Date:  2002-01-24       Impact factor: 49.962

4.  Intellectual outcome after reduced-dose radiation therapy plus adjuvant chemotherapy for medulloblastoma: a Children's Cancer Group study.

Authors:  M D Ris; R Packer; J Goldwein; D Jones-Wallace; J M Boyett
Journal:  J Clin Oncol       Date:  2001-08-01       Impact factor: 44.544

5.  The SmoA1 mouse model reveals that notch signaling is critical for the growth and survival of sonic hedgehog-induced medulloblastomas.

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6.  TrkC expression predicts good clinical outcome in primitive neuroectodermal brain tumors.

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Review 7.  ERBB2 in pediatric cancer: innocent until proven guilty.

Authors:  Richard J Gilbertson
Journal:  Oncologist       Date:  2005-08

8.  Clinical, histopathologic, and molecular markers of prognosis: toward a new disease risk stratification system for medulloblastoma.

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Journal:  J Clin Oncol       Date:  2004-02-17       Impact factor: 44.544

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10.  Metastatic medulloblastoma: the experience of the French Cooperative M7 Group.

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1.  Subsequent neoplasms in survivors of childhood central nervous system tumors: risk after modern multimodal therapy.

Authors:  Karen Tsui; Amar Gajjar; Chenghong Li; Deokumar Srivastava; Alberto Broniscer; Cynthia Wetmore; Larry E Kun; Thomas E Merchant; David W Ellison; Brent A Orr; Frederick A Boop; Paul Klimo; Jordan Ross; Leslie L Robison; Gregory T Armstrong
Journal:  Neuro Oncol       Date:  2014-11-13       Impact factor: 12.300

Review 2.  Childhood medulloblastoma: current status of biology and treatment.

Authors:  Laura J Klesse; Daniel C Bowers
Journal:  CNS Drugs       Date:  2010-04       Impact factor: 5.749

3.  Cardiorespiratory fitness in survivors of pediatric posterior fossa tumor.

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4.  High levels of PROM1 (CD133) transcript are a potential predictor of poor prognosis in medulloblastoma.

Authors:  Alessandro Raso; Samantha Mascelli; Roberto Biassoni; Paolo Nozza; Marcel Kool; Angela Pistorio; Elisabetta Ugolotti; Claudia Milanaccio; Sara Pignatelli; Manuela Ferraro; Marco Pavanello; Marcello Ravegnani; Armando Cama; Maria Luisa Garrè; Valeria Capra
Journal:  Neuro Oncol       Date:  2011-04-12       Impact factor: 12.300

5.  Heparanase Modulates Shh and Wnt3a Signaling in Human Medulloblastoma Cells.

Authors:  Lon D Ridgway; Michael D Wetzel; Dario Marchetti
Journal:  Exp Ther Med       Date:  2011-03-01       Impact factor: 2.447

6.  Morphological brain lesions of pediatric cerebellar tumor survivors correlate with inferior neurocognitive function but do not affect health-related quality of life.

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7.  Meningiomas of the pediatric skull base: a review.

Authors:  William C Gump
Journal:  J Neurol Surg B Skull Base       Date:  2014-09-21

8.  Comparison of risk of radiogenic second cancer following photon and proton craniospinal irradiation for a pediatric medulloblastoma patient.

Authors:  Rui Zhang; Rebecca M Howell; Annelise Giebeler; Phillip J Taddei; Anita Mahajan; Wayne D Newhauser
Journal:  Phys Med Biol       Date:  2013-01-16       Impact factor: 3.609

Review 9.  Children's Oncology Group's 2013 blueprint for research: central nervous system tumors.

Authors:  Amar Gajjar; Roger J Packer; N K Foreman; Kenneth Cohen; Daphne Haas-Kogan; Thomas E Merchant
Journal:  Pediatr Blood Cancer       Date:  2012-12-19       Impact factor: 3.167

10.  Systems biology-based drug repositioning identifies digoxin as a potential therapy for groups 3 and 4 medulloblastoma.

Authors:  Lei Huang; Sarah Garrett Injac; Kemi Cui; Frank Braun; Qi Lin; Yuchen Du; Huiyuan Zhang; Mari Kogiso; Holly Lindsay; Sibo Zhao; Patricia Baxter; Adesina Adekunle; Tsz-Kwong Man; Hong Zhao; Xiao-Nan Li; Ching C Lau; Stephen T C Wong
Journal:  Sci Transl Med       Date:  2018-10-24       Impact factor: 17.956

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