Literature DB >> 24516024

Impact of craniospinal dose, boost volume, and neurologic complications on intellectual outcome in patients with medulloblastoma.

Iska Moxon-Emre1, Eric Bouffet1, Michael D Taylor1, Normand Laperriere1, Nadia Scantlebury1, Nicole Law1, Brenda J Spiegler1, David Malkin1, Laura Janzen1, Donald Mabbott2.   

Abstract

PURPOSE: To examine the impact of radiation (ie, craniospinal irradiation [CSR] dose and boost volume) and complications (ie, hydrocephalus and other neurologic complications, including mutism) on patterns of change in intellectual functioning in medulloblastoma survivors. PATIENTS AND METHODS: We conducted a retrospective review of 113 patients treated for medulloblastoma between 1983 and 2011 who were seen for neuropsychological assessment, including longitudinal follow-up of intellectual function. Patients were treated with either standard-dose CSR with a posterior fossa (PF) boost (n=51), standard-dose CSR plus tumor bed (TB) boost (n=9), reduced-dose CSR plus PF boost (n=28), or reduced-dose CSR plus TB boost (n=23), with or without chemotherapy. A subset of patients developed hydrocephalus that required cerebrospinal fluid (CSF) diversion (n=54) and/or other neurologic complications (n=40), more than half of which were postoperative mutism (n=25). Growth curve analysis was used to determine stability or change in intelligence scores over time.
RESULTS: Patients treated with reduced-dose CSR plus TB boost showed stable intellectual trajectories, whereas patients treated with higher doses and larger boost volumes experienced intellectual declines. Presence of complications was associated with worse intellectual outcome; however, hydrocephalus requiring CSF diversion and mutism differed in their pattern of decline.
CONCLUSION: These results improve our understanding of factors that impair intellectual outcome in patients treated for medulloblastoma. Lower doses of CSR and smaller boost volumes seem to mitigate intellectual decline. Our findings validate the use of TB boost and suggest PF boost should be reconsidered.
© 2014 by American Society of Clinical Oncology.

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Year:  2014        PMID: 24516024     DOI: 10.1200/JCO.2013.52.3290

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


  69 in total

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Journal:  Childs Nerv Syst       Date:  2017-08-02       Impact factor: 1.475

2.  Visualization and segmentation of reciprocal cerebrocerebellar pathways in the healthy and injured brain.

Authors:  Nicole Law; Mark Greenberg; Eric Bouffet; Suzanne Laughlin; Michael D Taylor; David Malkin; Fang Liu; Iska Moxon-Emre; Nadia Scantlebury; Jovanka Skocic; Donald Mabbott
Journal:  Hum Brain Mapp       Date:  2015-04-14       Impact factor: 5.038

3.  Assessment of cognitive and neural recovery in survivors of pediatric brain tumors in a pilot clinical trial using metformin.

Authors:  Ramy Ayoub; Rebecca M Ruddy; Elizabeth Cox; Adeoye Oyefiade; Daniel Derkach; Suzanne Laughlin; Benjamin Ades-Aron; Zahra Shirzadi; Els Fieremans; Bradley J MacIntosh; Cynthia B de Medeiros; Jovanka Skocic; Eric Bouffet; Freda D Miller; Cindi M Morshead; Donald J Mabbott
Journal:  Nat Med       Date:  2020-07-27       Impact factor: 53.440

4.  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

5.  High expression of the transcriptional coactivator TAZ is associated with a worse prognosis and affects cell proliferation in patients with medulloblastoma.

Authors:  Hao Wang; Ji Zhou; Dong Yang; Liang Yi; Xuhui Wang; Yangqing Ou; Donghong Yang; Lunshan Xu; Minhui Xu
Journal:  Oncol Lett       Date:  2019-09-11       Impact factor: 2.967

6.  Dose-volume metrics and their relation to memory performance in pediatric brain tumor patients: A preliminary study.

Authors:  Kimberly P Raghubar; Michael Lamba; Kim M Cecil; Keith Owen Yeates; E Mark Mahone; Christina Limke; David Grosshans; Travis J Beckwith; M Douglas Ris
Journal:  Pediatr Blood Cancer       Date:  2018-06-01       Impact factor: 3.167

7.  Low- and middle-income countries can reduce risks of subsequent neoplasms by referring pediatric craniospinal cases to centralized proton treatment centers.

Authors:  Phillip J Taddei; Nabil Khater; Bassem Youssef; Rebecca M Howell; Wassim Jalbout; Rui Zhang; Fady B Geara; Annelise Giebeler; Anita Mahajan; Dragan Mirkovic; Wayne D Newhauser
Journal:  Biomed Phys Eng Express       Date:  2018-02-07

8.  Long-term health-related quality of life in pediatric brain tumor survivors receiving proton radiotherapy at <4 years of age.

Authors:  Bree R Eaton; Saveli Goldberg; Nancy J Tarbell; Miranda P Lawell; Sara L Gallotto; Elizabeth A Weyman; Karen A Kuhlthau; David H Ebb; Shannon M MacDonald; Torunn I Yock
Journal:  Neuro Oncol       Date:  2020-09-29       Impact factor: 12.300

Review 9.  Medulloblastoma development: tumor biology informs treatment decisions.

Authors:  Vidya Gopalakrishnan; Rong-Hua Tao; Tara Dobson; William Brugmann; Soumen Khatua
Journal:  CNS Oncol       Date:  2015

Review 10.  Proton therapy for paediatric CNS tumours - improving treatment-related outcomes.

Authors:  Vinai Gondi; Torunn I Yock; Minesh P Mehta
Journal:  Nat Rev Neurol       Date:  2016-05-20       Impact factor: 42.937

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