Literature DB >> 22851561

Hyperfractionated versus conventional radiotherapy followed by chemotherapy in standard-risk medulloblastoma: results from the randomized multicenter HIT-SIOP PNET 4 trial.

Birgitta Lannering1, Stefan Rutkowski, Francois Doz, Barry Pizer, Göran Gustafsson, Aurora Navajas, Maura Massimino, Roel Reddingius, Martin Benesch, Christian Carrie, Roger Taylor, Lorenza Gandola, Thomas Björk-Eriksson, Jordi Giralt, Foppe Oldenburger, Torsten Pietsch, Dominique Figarella-Branger, Keith Robson, Marco Forni, Steven C Clifford, Monica Warmuth-Metz, Katja von Hoff, Andreas Faldum, Véronique Mosseri, Rolf Kortmann.   

Abstract

PURPOSE: To compare event-free survival (EFS), overall survival (OS), pattern of relapse, and hearing loss in children with standard-risk medulloblastoma treated by postoperative hyperfractionated or conventionally fractionated radiotherapy followed by maintenance chemotherapy. PATIENTS AND METHODS: In all, 340 children age 4 to 21 years from 122 European centers were postoperatively staged and randomly assigned to treatment with hyperfractionated radiotherapy (HFRT) or standard (conventional) fractionated radiotherapy (STRT) followed by a common chemotherapy regimen consisting of eight cycles of cisplatin, lomustine, and vincristine.
RESULTS: After a median follow-up of 4.8 years (range, 0.1 to 8.3 years), survival rates were not significantly different between the two treatment arms: 5-year EFS was 77% ± 4% in the STRT group and 78% ± 4% in the HFRT group; corresponding 5-year OS was 87% ± 3% and 85% ± 3%, respectively. A postoperative residual tumor of more than 1.5 cm(2) was the strongest negative prognostic factor. EFS of children with all reference assessments and no large residual tumor was 82% ± 2% at 5 years. Patients with a delay of more than 7 weeks to the start of RT had a worse prognosis. Severe hearing loss was not significantly different for the two treatment arms at follow-up.
CONCLUSION: In this large randomized European study, which enrolled patients with standard-risk medulloblastoma from more than 100 centers, excellent survival rates were achieved in patients without a large postoperative residual tumor and without RT treatment delays. EFS and OS for HFRT was not superior to STRT, which therefore remains standard of care in this disease.

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Year:  2012        PMID: 22851561     DOI: 10.1200/JCO.2011.39.8719

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  94 in total

1.  Quality of life in long-term survivors treated for metastatic medulloblastoma with a hyperfractionated accelerated radiotherapy (HART) strategy.

Authors:  L Veneroni; L Boschetti; F Barretta; C A Clerici; F Simonetti; E Schiavello; V Biassoni; F Spreafico; L Gandola; E Pecori; B Diletto; G Poggi; F Gariboldi; R Sensi; M Massimino
Journal:  Childs Nerv Syst       Date:  2017-08-02       Impact factor: 1.475

2.  Improving the quality of care in the molecular era for children and adolescents with medulloblastoma.

Authors:  T de Rojas; M Puertas; F Bautista; I de Prada; M Á López-Pino; B Rivero; C Gonzalez-San Segundo; M Gonzalez-Vicent; A Lassaletta; L Madero; L Moreno
Journal:  Clin Transl Oncol       Date:  2019-04-01       Impact factor: 3.405

3.  Nanoparticle-mediated knockdown of DNA repair sensitizes cells to radiotherapy and extends survival in a genetic mouse model of glioblastoma.

Authors:  Forrest M Kievit; Kui Wang; Tatsuya Ozawa; Aria W Tarudji; John R Silber; Eric C Holland; Richard G Ellenbogen; Miqin Zhang
Journal:  Nanomedicine       Date:  2017-06-11       Impact factor: 5.307

Review 4.  [Not Available].

Authors:  M Warmuth-Metz; B Bison
Journal:  Clin Neuroradiol       Date:  2015-05-21       Impact factor: 3.649

Review 5.  The clinical importance of medulloblastoma extent of resection: a systematic review.

Authors:  Eric M Thompson; Alexa Bramall; James E Herndon; Michael D Taylor; Vijay Ramaswamy
Journal:  J Neurooncol       Date:  2018-05-23       Impact factor: 4.130

Review 6.  Response assessment in medulloblastoma and leptomeningeal seeding tumors: recommendations from the Response Assessment in Pediatric Neuro-Oncology committee.

Authors:  Katherine E Warren; Gilbert Vezina; Tina Y Poussaint; Monika Warmuth-Metz; Marc C Chamberlain; Roger J Packer; Alba A Brandes; Moshe Reiss; Stewart Goldman; Michael J Fisher; Ian F Pollack; Michael D Prados; Patrick Y Wen; Susan M Chang; Christelle Dufour; David Zurakowski; Rolf D Kortmann; Mark W Kieran
Journal:  Neuro Oncol       Date:  2018-01-10       Impact factor: 12.300

7.  Child-related characteristics predicting subsequent health-related quality of life in 8- to 14-year-old children with and without cerebellar tumors: a prospective longitudinal study.

Authors:  Kim S Bull; Christina Liossi; David Culliford; Janet L Peacock; Colin R Kennedy
Journal:  Neurooncol Pract       Date:  2014-08-11

8.  [Hyperfractionated vs. conventionally fractionated radiotherapy of nonmetastatic medulloblastoma].

Authors:  R-D Kortmann; H-J Ochel
Journal:  Strahlenther Onkol       Date:  2013-03       Impact factor: 3.621

9.  Hippocampal sparing radiotherapy for pediatric medulloblastoma: impact of treatment margins and treatment technique.

Authors:  N Patrik Brodin; Per Munck af Rosenschöld; Malin Blomstrand; Anne Kiil-Berthlesen; Christian Hollensen; Ivan R Vogelius; Birgitta Lannering; Søren M Bentzen; Thomas Björk-Eriksson
Journal:  Neuro Oncol       Date:  2013-12-09       Impact factor: 12.300

Review 10.  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

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