Pegylated interferon-α-2b for children with recurrent craniopharyngioma Clinical article

被引:20
作者
Yeung, Jacky T. [2 ]
Pollack, Ian F. [3 ]
Panigrahy, Ashok [4 ]
Jakacki, Regina I. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Childrens Hosp Pittsburgh, Dept Pediat, Pittsburgh, PA 15224 USA
[2] Univ Pittsburgh, Sch Med, Dept Neurosurg, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Neurosurg, Childrens Hosp Pittsburgh, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Sch Med, Dept Radiol, Childrens Hosp Pittsburgh, Pittsburgh, PA USA
关键词
recurrent craniopharyngioma; pegylated interferon; pediatric neurosurgery; oncology; SQUAMOUS-CELL CARCINOMA; INTRATUMORAL CHEMOTHERAPY; RADIATION-THERAPY; CYSTIC-CRANIOPHARYNGIOMA; ALPHA-INTERFERON; SURGERY; GROWTH; COMBINATION; MANAGEMENT; SEQUELAE;
D O I
10.3171/2012.9.PEDS12225
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Previous studies of systemic and intralesional administration of nonpegylated interferon have shown efficacy against craniopharyngioma. Pegylaion of interferon-alpha-2b (PI) prolongs the half-life, allowing sustained exposure of the drug over time, and enhances efficacy. The authors report the results of the use of 131 in 5 children with recurrent craniopharyngiomas. Methods. Five children, ranging in age from 9 to 15 years, with recurrent craniopharyngiomas were treated for up to 2 years with subcutaneous injections of PI at a dose of 1-3 mu g/kg/week. Tumor response was assessed using MRI. Results. All patients had stable disease or better in response to PI. One patient experienced a recurrence after gross-total resection (GTR). She initially showed an increase in the predominantly cystic tumor after 3 months of treatment, followed by a complete response. She required no further intervention and remains without evidence of disease 10 years after starting treatment. Another patient experienced recurrence 3.3 years after subtotal resection (STR) and radiation therapy. He had complete disappearance of the predominantly cystic component after 4 months of treatment, and a small residual calcified mass remains 5 years later. The third patient experienced recurrence after 3 GTRs. He had a complete response after 7 months of treatment and remains without evidence of disease 19 months after starting treatment. The fourth patient experienced recurrence after 2 STRs. He had a 30% decrease in tumor size after 4 months of treatment, which was maintained for 12 months at which point the cyst began to increase in size. The final patient experienced recurrence after GTR and has stable disease 6 months after starting treatment with PI. Conclusions. The use of PI in children with recurrent craniopharyngiomas can result in significant and durable responses and potentially delay or avoid the need for radiation therapy. (http://thejns.org/doi/abs/10.3171/2012.9.PEDS12225)
引用
收藏
页码:498 / 503
页数:6
相关论文
共 33 条
[1]   The descriptive epidemiology of craniopharyngioma [J].
Bunin, GR ;
Surawicz, TS ;
Witman, PA ;
Preston-Martin, S ;
Davis, F ;
Bruner, JM .
JOURNAL OF NEUROSURGERY, 1998, 89 (04) :547-551
[2]   Use of interferon alpha in intratumoral chemotherapy for cystic craniopharyngioma [J].
Cavalheiro, S ;
Dastoli, PA ;
Silva, NS ;
Toledo, S ;
Lederman, H ;
da Silva, MC .
CHILDS NERVOUS SYSTEM, 2005, 21 (8-9) :719-724
[3]   Craniopharyngiomas: intratumoral chemotherapy with interferon-α: a multicenter preliminary study with 60 cases [J].
Cavalheiro, Sergio ;
Di Rocco, Concezzio ;
Valenzuela, Sergio ;
Dastoli, Patricia A. ;
Tamburrini, Gianpiero ;
Massimi, Lucca ;
Nicacio, Jardel M. ;
Faquini, Igor V. ;
Ierardi, Daniela F. ;
Silva, Nasjla S. ;
Pettorini, Benedetta Ludovica ;
Toledo, Silvia R. C. .
NEUROSURGICAL FOCUS, 2010, 28 (04) :E12.1-E12.5
[4]   NEUROLOGICAL AND PSYCHOPHYSIOLOGICAL SEQUELAE FOLLOWING DIFFERENT TREATMENTS OF CRANIOPHARYNGIOMA IN CHILDREN [J].
CAVAZZUTI, V ;
FISCHER, EG ;
WELCH, K ;
BELLI, JA ;
WINSTON, KR .
JOURNAL OF NEUROSURGERY, 1983, 59 (03) :409-417
[5]  
CHOUX M, 1991, Neurochirurgie, V37, P1
[6]   Cystic craniopharyngioma Intratumoral chemotherapy with alpha interferon [J].
Dastoli, Patricia Alessandra ;
Nicacio, Jardel Mendonca ;
Silva, Nasjla Saba ;
Capellano, Andrea Maria ;
Toledo, Silvia R. C. ;
Ierardi, Daniela ;
Cavalheiro, Sergio .
ARQUIVOS DE NEURO-PSIQUIATRIA, 2011, 69 (01) :50-55
[7]   Growth and endocrine sequelae of craniopharyngioma [J].
DeVile, CJ ;
Grant, DB ;
Hayward, RD ;
Stanhope, R .
ARCHIVES OF DISEASE IN CHILDHOOD, 1996, 75 (02) :108-114
[8]   TREATMENT OF CUTANEOUS SQUAMOUS-CELL CARCINOMAS BY INTRALESIONAL INTERFERON ALFA-2B THERAPY [J].
EDWARDS, L ;
BERMAN, B ;
RAPINI, RP ;
WHITING, DA ;
TYRING, S ;
GREENWAY, HT ;
EYRE, SP ;
TANNER, DJ ;
TAYLOR, EL ;
PEETS, E ;
SMILES, KA .
ARCHIVES OF DERMATOLOGY, 1992, 128 (11) :1486-1489
[9]   Efficacy and safety of radical resection of primary and recurrent craniopharyngiomas in 86 children Clinical article [J].
Elliott, Robert E. ;
Hsieh, Kevin ;
Hochman, Tsivia ;
Belitskaya-Levy, Ilana ;
Wisoff, Jessica ;
Wisoff, Jeffrey H. .
JOURNAL OF NEUROSURGERY-PEDIATRICS, 2010, 5 (01) :30-48
[10]  
HERTZOG PJ, 1994, MOL REPROD DEV, V39, P226