Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Am J Clin Oncol. 2012 Feb;35(1):51-7. doi: 10.1097/COC.0b013e318201a2b7.
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.
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.
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.
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.
弥漫性内在脑桥胶质瘤(DIPG)是高度侵袭性肿瘤,预后较差。几乎所有患者在接受确定性治疗后都会出现疾病进展,伴有严重的神经功能缺损和发病率。在这里,我们报告了一系列接受再放疗以缓解症状的患者。
2007 年至 2009 年,MD 安德森癌症中心的 6 名患者因进展性 DIPG 接受了再放疗。在再放疗之前,通过临床和磁共振成像确认了初始放化疗和挽救性化疗后的进展。每个病例都在多学科会议上进行了讨论。
初始放疗和再放疗之间的间隔为 8 至 28 个月。初始放疗剂量为 54 至 55.8Gy。初始进展时间为 4 至 18 个月。所有患者在挽救性化疗后均进一步进展。再放疗与同期化疗联合使用,剂量为 20Gy(n=4)或 18Gy(n=1);1 例患者在单次 2Gy 剂量后撤回治疗。4 例患者的症状有明显改善,言语(n=3)、共济失调(n=3)和吞咽困难(n=2)。3 例患者在再放疗后重新具有行走能力。4 例患者在治疗后磁共振成像上肿瘤体积缩小。中位临床无进展生存期为 5 个月。急性放射性相关毒性为疲劳(n=2)、脱发(n=2)和食欲减退(n=1)。无 3 级或 4 级毒性反应。
化疗再放疗可能是可行的,可改善症状并延迟进展,毒性最小。最有可能受益的患者可能是那些对初始治疗反应时间长且初始放疗后间隔时间长的患者。