Literature DB >> 24661654

Postponed is not canceled: role of craniospinal radiation therapy in the management of recurrent infant medulloblastoma--an experience from the HIT-REZ 1997 & 2005 studies.

Klaus Müller1, Martin Mynarek2, Isabella Zwiener3, Nele Siegler4, Martina Zimmermann5, Hans Christiansen6, Wilfried Budach7, Guido Henke8, Monika Warmuth-Metz9, Torsten Pietsch10, Katja von Hoff2, Andre von Bueren11, Udo Bode5, Stefan Rutkowski2, Rolf-Dieter Kortmann12, Gudrun Fleischhack4, Stephan Tippelt4.   

Abstract

PURPOSE: To evaluate the efficacy of craniospinal irradiation (CSI) in the management of recurrent infant medulloblastoma after surgery and chemotherapy alone. METHODS AND MATERIALS: Seventeen pediatric medulloblastoma patients registered in the HIT-REZ 1997 and 2005 studies underwent CSI as salvage treatment at first recurrence. All patients had achieved complete remission after first-line treatment consisting of surgery and chemotherapy. Eleven patients showed metastatic disease at relapse. Five patients underwent surgery prior to radiation therapy, which resulted in complete resection in 1 case. In 1 patient, complete resection of the residual tumor was performed after CSI. Eleven patients received chemotherapy prior, 6 patients during and 8 patients after CSI. All patients received CSI with a median total dose of 35.2 Gy, and all but 1 received a boost to the posterior fossa (median total dose, 55.0 Gy). Metastases were boosted with an individual radiation dose, depending on their location and extent.
RESULTS: During a median follow-up time of 6.2 years since recurrence, 11 patients showed progressive disease and died. Median progression-free (overall) survival was 2.9 ± 1.1 (3.8 ± 0.8) years. Progression-free survival (PFS) rates at 1, 3, and 5 years were 88% ± 8%, 46% ± 12%, and 40% ± 12%, respectively. Overall survival (OS) rates at 1, 3, and 5 years were 94% ± 6%, 58% ± 12%, and 39% ± 12%, respectively. For 11 patients with classic medulloblastoma, 3-year (and 5-year) PFS and OS were 62% ± 15% and 72% ± 14% (52% ± 16% and 51% ± 16%), respectively. On univariate analysis, metastatic disease was not associated with poorer progression-free and overall survival.
CONCLUSIONS: Our results suggest that salvage treatment of relapsed medulloblastomas consisting of CSI and chemotherapy offers a second chance for cure, even for patients with classic histological findings. Metastatic disease at relapse did not have an impact on survival. However, this may be explained by the small number of patients.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24661654     DOI: 10.1016/j.ijrobp.2014.01.013

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  7 in total

1.  The kinesin KIF14 is overexpressed in medulloblastoma and downregulation of KIF14 suppressed tumor proliferation and induced apoptosis.

Authors:  Kay Ka-Wai Li; Yan Qi; Tian Xia; Aden Ka-Yin Chan; Zhen-Yu Zhang; Abudumijiti Aibaidula; Rong Zhang; Liangfu Zhou; Yu Yao; Ho-Keung Ng
Journal:  Lab Invest       Date:  2017-05-15       Impact factor: 5.662

Review 2.  Medulloblastoma.

Authors:  Nathan E Millard; Kevin C De Braganca
Journal:  J Child Neurol       Date:  2015-09-02       Impact factor: 1.987

3.  Clinical, Pathological, and Molecular Characterization of Infant Medulloblastomas Treated with Sequential High-Dose Chemotherapy.

Authors:  Lucie Lafay-Cousin; Amy Smith; Susan N Chi; Elizabeth Wells; Jennifer Madden; Ashley Margol; Vijay Ramaswamy; Jonathan Finlay; Michael D Taylor; Girish Dhall; Douglas Strother; Mark W Kieran; Nicholas K Foreman; Roger J Packer; Eric Bouffet
Journal:  Pediatr Blood Cancer       Date:  2016-05-04       Impact factor: 3.167

4.  Bridging the treatment gap in infant medulloblastoma: molecularly informed outcomes of a globally feasible regimen.

Authors:  Lorena V Baroni; Claudia Sampor; Adriana Gonzalez; Fabiana Lubieniecki; Gabriela Lamas; Carlos Rugilo; Ute Bartels; Ayala Heled; Kyle S Smith; Paul A Northcott; Eric Bouffet; Daniel Alderete; Vijay Ramaswamy
Journal:  Neuro Oncol       Date:  2020-12-18       Impact factor: 12.300

5.  Time, pattern, and outcome of medulloblastoma relapse and their association with tumour biology at diagnosis and therapy: a multicentre cohort study.

Authors:  Rebecca M Hill; Stacey Richardson; Edward C Schwalbe; Debbie Hicks; Janet C Lindsey; Stephen Crosier; Gholamreza Rafiee; Yura Grabovska; Stephen B Wharton; Thomas S Jacques; Antony Michalski; Abhijit Joshi; Barry Pizer; Daniel Williamson; Simon Bailey; Steven C Clifford
Journal:  Lancet Child Adolesc Health       Date:  2020-10-22

6.  Local and Systemic Therapy of Recurrent Medulloblastomas in Children and Adolescents: Results of the P-HIT-REZ 2005 Study.

Authors:  Christine Gaab; Jonas E Adolph; Stephan Tippelt; Ruth Mikasch; Denise Obrecht; Martin Mynarek; Stefan Rutkowski; Stefan M Pfister; Till Milde; Olaf Witt; Brigitte Bison; Monika Warmuth-Metz; Rolf-Dieter Kortmann; Stefan Dietzsch; Torsten Pietsch; Beate Timmermann; Ronald Sträter; Udo Bode; Andreas Faldum; Robert Kwiecien; Gudrun Fleischhack
Journal:  Cancers (Basel)       Date:  2022-01-18       Impact factor: 6.639

7.  Treatment of children under 4 years of age with medulloblastoma and ependymoma in the HIT2000/HIT-REZ 2005 trials: Neuropsychological outcome 5 years after treatment.

Authors:  Holger Ottensmeier; Paul G Schlegel; Matthias Eyrich; Johannes E Wolff; Björn-Ole Juhnke; Katja von Hoff; Stefanie Frahsek; Rene Schmidt; Andreas Faldum; Gudrun Fleischhack; Andre von Bueren; Carsten Friedrich; Anika Resch; Monika Warmuth-Metz; Jürgen Krauss; Rolf D Kortmann; Udo Bode; Joachim Kühl; Stefan Rutkowski
Journal:  PLoS One       Date:  2020-01-23       Impact factor: 3.240

  7 in total

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