Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma

Author:

Fouladi Maryam1,Chintagumpala Murali1,Ashley David1,Kellie Stewart1,Gururangan Sridharan1,Hassall Tim1,Gronewold Lindsey1,Stewart Clinton F.1,Wallace Dana1,Broniscer Alberto1,Hale Gregory A.1,Kasow Kimberly A.1,Merchant Thomas E.1,Morris Brannon1,Krasin Matthew1,Kun Larry E.1,Boyett James M.1,Gajjar Amar1

Affiliation:

1. From the Departments of Oncology, Biostatistics, Pharmaceutical Sciences, Radiological Sciences, St Jude Children's Research Hospital, Memphis, TN; Baylor College of Medicine, Houston, TX, Royal Children's Hospital, Melbourne, Australia; Children's Hospital at Westmead, Sydney, Australia; Royal Children's Hospital, Brisbane, Australia; and The Preston Robert Tisch Brain Tumor Center and Departments of Pediatrics and Surgery, Duke University Medical Center, Durham, NC

Abstract

Purpose To determine the role of amifostine as a protectant against cisplatin-induced ototoxicity in patients with average-risk (AR) medulloblastoma treated with craniospinal radiotherapy and four cycles of cisplatin-based, dose-intense chemotherapy and stem-cell rescue. Patients and Methods The primary objective was to determine whether, in patients with AR medulloblastoma (n = 62), amifostine would decrease the need for hearing aids (defined as ≥ grade 3 ototoxicity in one ear) compared with a control group (n = 35), 1 year from initiating treatment. Ninety-seven patients received craniospinal irradiation (23.4 Gy) followed by 55.8 Gy to the primary tumor bed using three-dimensional conformal technique, and four cycles of high-dose cyclophosphamide (4,000 mg/m2/cycle), cisplatin (75 mg/m2/cycle), and vincristine (two 1.5 mg/m2 doses/cycle) and stem-cell rescue. When used, amifostine (600 mg/m2/dose) was administered as a bolus immediately before and 3 hours into the cisplatin infusion. Results The median age of the 97 patients was 8.7 years (range, 3.2 to 20.2 years). The study and control groups were similar in age and sex distribution. Amifostine was well-tolerated. One year after treatment initiation, 13 patients (37.1%) in the control group versus nine (14.5%; one-sided χ2 test P = .005) of the amifostine-treated patients had at least grade 3 ototoxicity, requiring hearing aid in at least one ear. Conclusion Amifostine administered before and during the cisplatin infusion can significantly reduce the risk of severe ototoxicity in patients with AR medulloblastoma receiving dose-intense chemotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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