Literature DB >> 20931205

Carboplatin and ototoxicity: hearing loss rates among survivors of childhood medulloblastoma.

Lindy Musial-Bright1, Rüdiger Fengler, Günter Henze, Pablo Hernáiz Driever.   

Abstract

PURPOSE: Patients with medulloblastoma are exposed to ototoxic treatments including radiation therapy and platinum chemotherapy. The favorable toxicity profile of carboplatin led us to substitute this chemotherapeutic agent for cisplatin in the HIT-1991, HIT-MED-1999, and HIT-2000 chemotherapy protocols. We retrospectively investigated its consequences in terms of overall survival and ototoxicity rates.
METHODS: Twenty-four medulloblastoma patients were treated according to HIT protocols with carboplatin substitution between April 1999 and June 2006. Nineteen (79%) patients had adequate baseline and post-treatment audiological data. Mean age at diagnosis was 9.3 (range 3.5-18.9) years with a mean follow-up time of 30.8 (8.1-111.3) months. Patients received a mean carboplatin cumulative dose of 2,131 (830-4312) mg/m(2).
RESULTS: Twenty-three patients were alive at the time of assessment. Hearing loss greater than 20 dB was observed in two (10.5%) of 19 patients. Both had grade 2 ototoxicity according to Brock's scale. There were no significant differences between the patients' baseline and post-treatment audiograms at any frequency. The observed hearing loss was significantly correlated to younger age at diagnosis and cumulative carboplatin dose (p<0.05).
CONCLUSIONS: The encouraging overall survival and low hearing loss rates in this medulloblastoma patient cohort suggest that protocols containing carboplatin may offer a viable alternative to standard cisplatin protocols and warrant further investigation. © Springer-Verlag 2010

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Year:  2010        PMID: 20931205     DOI: 10.1007/s00381-010-1300-1

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  38 in total

1.  Risks of young age for selected neurocognitive deficits in medulloblastoma are associated with white matter loss.

Authors:  R K Mulhern; S L Palmer; W E Reddick; J O Glass; L E Kun; J Taylor; J Langston; A Gajjar
Journal:  J Clin Oncol       Date:  2001-01-15       Impact factor: 44.544

Review 2.  Medulloblastoma: clinical and biologic aspects.

Authors:  R J Packer; P Cogen; G Vezina; L B Rorke
Journal:  Neuro Oncol       Date:  1999-07       Impact factor: 12.300

3.  Medulloblastoma in the second decade of life: a specific group with respect to toxicity and management: a Canadian Pediatric Brain Tumor Consortium Study.

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Journal:  Cancer       Date:  2005-05-01       Impact factor: 6.860

4.  Early changes in auditory function as a result of platinum chemotherapy: use of extended high-frequency audiometry and evoked distortion product otoacoustic emissions.

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Journal:  J Clin Oncol       Date:  2007-04-01       Impact factor: 44.544

5.  Ototoxicity of preradiation cisplatin for children with central nervous system tumors.

Authors:  C S Kretschmar; M P Warren; B L Lavally; S Dyer; N J Tarbell
Journal:  J Clin Oncol       Date:  1990-07       Impact factor: 44.544

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  16 in total

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2.  Long-Term Variability of Distortion-Product Otoacoustic Emissions in Infants and Children and Its Relation to Pediatric Ototoxicity Monitoring.

Authors:  Dawn Konrad-Martin; Kristin Knight; Garnett P McMillan; Laura E Dreisbach; Elsa Nelson; Marilyn Dille
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Review 4.  Apoptosis in acquired and genetic hearing impairment: the programmed death of the hair cell.

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5.  Protective effect of acetyl-l-carnitine against cisplatin ototoxicity: role of apoptosis-related genes and pro-inflammatory cytokines.

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8.  Prospective evaluation of cisplatin- and carboplatin-mediated ototoxicity in paediatric and adult soft tissue and osteosarcoma patients.

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9.  Dimethyl sulfoxide (DMSO) exacerbates cisplatin-induced sensory hair cell death in zebrafish (Danio rerio).

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Review 10.  Membrane transporters as mediators of Cisplatin effects and side effects.

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