Palliative Reirradiation for Progressive Diffuse Intrinsic Pontine Glioma

被引:52
|
作者
Fontanilla, Hiral P. [1 ]
Pinnix, Chelsea C. [1 ]
Ketonen, Leena M. [2 ]
Woo, Shiao Y. [1 ]
Vats, Tribhawan S. [3 ]
Rytting, Michael E. [3 ]
Wolff, Johannes E. [3 ]
Mahajan, Anita [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Pediat Neurooncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2012年 / 35卷 / 01期
关键词
brainstem glioma; palliative radiation; pediatric brain tumors; BRAIN-STEM GLIOMAS; RADIATION-THERAPY; CHILDREN; BEVACIZUMAB; TOLERANCE; CHEMOTHERAPY; RADIOTHERAPY; NECROSIS; VINCRISTINE;
D O I
10.1097/COC.0b013e318201a2b7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Diffuse intrinsic pontine gliomas (DIPGs) are highly aggressive tumors and have a poor prognosis. Nearly all patients experience disease progression after definitive treatment, accompanied by severe neurologic deficits and morbidity. Here, we report a series of patients treated with reirradiation for palliation of symptoms. Methods: Six patients received reirradiation for progressive DIPG at MD Anderson Cancer Center from 2007 to 2009. Progression after initial chemoradiation and salvage chemotherapy had been confirmed clinically and by magnetic resonance imaging. Each case was discussed at a multidisciplinary conference before reirradiation. Results: Interval between the initial radiation therapy and reirradiation was 8 to 28 months. The initial radiation therapy dose was 54 to 55.8 Gy. Time to initial progression was 4 to 18 months. All of the patients had further progression on salvage chemotherapy. Reirradiation was given with concurrent chemotherapy to a dose of 20 Gy (n=4) or 18 Gy (n=1); 1 patient withdrew care after a single 2-Gy fraction. Four patients had substantial clinical improvement in symptoms, with improvement in speech (n=3), ataxia (n=3), and swallowing (n=2). Three patients showed renewed ability to ambulate after reirradiation. Four patients had decreased tumor size on posttreatment magnetic resonance imaging. The median clinical progression-free survival time was 5 months. Acute radiation-related toxicities were fatigue (n=2), alopecia (n=2), and decreased appetite (n=1). No grade 3 or 4 toxicities were reported. Conclusions: Reirradiation with chemotherapy may be feasible to improve symptoms and delay progression with minimal toxicity. Patients who are most likely to benefit may be those with prolonged response to initial therapy and a long interval since initial radiation.
引用
收藏
页码:51 / 57
页数:7
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