Limited surgery and conformal photon radiation therapy for pediatric craniopharyngioma: long-term results from the RT1 protocol

被引:20
|
作者
Edmonston, Drucilla Y. [1 ]
Wu, Shengjie [2 ]
Li, Yimei [2 ]
Khan, Raja B. [3 ]
Boop, Frederick A. [4 ]
Merchant, Thomas E. [5 ]
机构
[1] Univ Tennessee, Hlth Sci Ctr, Dept Radiat Oncol, Memphis, TN USA
[2] St Jude Childrens Res Hosp, Dept Biostat, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Neurol, 332 N Lauderdale St, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Global Pediat Med, 332 N Lauderdale St, Memphis, TN 38105 USA
[5] St Jude Childrens Res Hosp, Dept Radiat Oncol, 262 Danny Thomas Pl,Mail Stop 210, Memphis, TN 38105 USA
关键词
craniopharyngioma; outcomes; pediatrics; radiotherapy; CHILDHOOD-ONSET; RADIOTHERAPY; MANAGEMENT; RESECTION; SURVIVAL; OUTCOMES; CHILDREN;
D O I
10.1093/neuonc/noac124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Our aim was to estimate long-term disease control and complications after conformal radiation therapy (CRT) in children and adolescents with craniopharyngioma. Materials and Methods Pediatric patients with craniopharyngioma (n = 101) were enrolled on or treated according to a phase II single institutional protocol from 1998. Surgery was individualized, and CRT (54Gy) was administered using a 1.0 cm or 0.5 cm clinical target volume margin. Patients were followed for 10 years by serial MR imaging and MR angiography and a battery of tests to measure the effects of treatment. Results Twenty patients had tumor progression. Twelve patients who had tumor progression died due to tumor (n = 6) or complications related to tumor or treatment (n = 6). With a median follow-up of 14.94 years for survivors, the 10 year estimates (+/- SE) of progression-free survival (PFS), event-free survival (EFS), and overall survival (OS) were 78.84% +/- 4.10%, 77.12% +/- 4.19%, and 96.02% +/- 1.95%, respectively. OS, EFS, and PFS were significantly associated with race, shunt status, and tumor volume. The 10 year cumulative incidence (+/- SE) of the secondary tumor (1.99% +/- 1.40%), secondary malignant tumor (1.0% +/- 1.0%), necrosis (1.98% +/- 1.39%), vasculopathy (8.47% +/- 2.90%), and permanent neurologic deficits (8.28% +/- 3.37%) were estimated by competing risk analysis. Three patients required revascularization surgery. Salvage therapy was successful in 13 patients using surgery and radiosurgery. Conclusions Limited surgery and CRT using photons results in excellent tumor control. Tumor control and the incidence and severity of complications are associated with host, tumor, and treatment factors.
引用
收藏
页码:2200 / 2209
页数:10
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