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质子治疗儿童室管膜瘤:来自双中心研究的成熟结果。

Proton Therapy for Pediatric Ependymoma: Mature Results From a Bicentric Study.

机构信息

Department of Radiation Oncology, University of Florida College of Medicine, Jacksonville, Florida.

Department of Radiation Oncology, Harvard Medical School, Boston, Massachusetts.

出版信息

Int J Radiat Oncol Biol Phys. 2021 Jul 1;110(3):815-820. doi: 10.1016/j.ijrobp.2021.01.027. Epub 2021 Jan 27.

Abstract

PURPOSE

To report the long-term efficacy and toxicity of proton therapy for pediatric ependymoma.

METHODS AND MATERIALS

Between 2000 and 2019, 386 children with nonmetastatic grade 2/3 intracranial ependymoma received proton therapy at 1 of 2 academic institutions. Median age at treatment was 3.8 years (range, 0.7-21.3); 56% were male. Most (72%) tumors were in the posterior fossa and classified as World Health Organization grade 3 (65%). Eighty-five percent had a gross total or near total tumor resection before radiation therapy; 30% received chemotherapy. Median radiation dose was 55.8 Gy relative biologic effectiveness (RBE) (range, 50.4-59.4).

RESULTS

Median follow-up was 5.0 years (range, 0.4-16.7). The 7-year local control, progression-free survival, and overall survival rates were 77.0% (95% confidence interval [CI], 71.9%-81.5%), 63.8% (95% CI, 58.0%-68.8%), and 82.2% (95% CI, 77.2%-86.3%), respectively. Subtotal resection was associated with inferior local control (59% vs 80%; P < .005), progression-free survival (48% vs 66%; P < .001), and overall survival (70% vs 84%; P < .05). Male sex was associated with inferior progression-free (60% vs 69%; P < .05) and overall survival (76% vs 89%; P < .05). Posterior fossa tumor site was also associated with inferior progression-free (59% vs 74%; P < .05) and overall survival (79% vs 89%; P < .01). Twenty-one patients (5.4%) required hearing aids; of these, 13 received cisplatin, including the 3 with bilateral hearing loss. Forty-five patients (11.7%) required hormone replacement, typically growth hormone (38/45). The cumulative incidence of grade 2+ brain stem toxicity was 4% and occurred more often in patients who received >54 GyRBE. Two patients (0.5%) died of brain stem necrosis. The second-malignancy rate was 0.8%.

CONCLUSION

Proton therapy offers disease control commensurate with modern photon therapy without unexpected toxicity. The high rate of long-term survival justifies efforts to reduce radiation exposure in this young population. Independent of radiation modality, this large series confirms extent of resection as the most important modifiable factor for survival.

摘要

目的

报告质子治疗儿童室管膜瘤的长期疗效和毒性。

方法和材料

在 2000 年至 2019 年间,2 家学术机构的 386 名患有非转移性 2/3 级颅内室管膜瘤的儿童接受了质子治疗。治疗时的中位年龄为 3.8 岁(范围,0.7-21.3);56%为男性。大多数(72%)肿瘤位于后颅窝,分类为世界卫生组织 3 级(65%)。85%的患者在放射治疗前进行了大体全切除或近全切除;30%接受了化疗。中位放射剂量为 55.8Gy 相对生物效应(RBE)(范围,50.4-59.4)。

结果

中位随访时间为 5.0 年(范围,0.4-16.7)。7 年局部控制率、无进展生存率和总生存率分别为 77.0%(95%置信区间[CI],71.9%-81.5%)、63.8%(95%CI,58.0%-68.8%)和 82.2%(95%CI,77.2%-86.3%)。次全切除与局部控制不良相关(59% vs 80%;P<.005)、无进展生存率(48% vs 66%;P<.001)和总生存率(70% vs 84%;P<.05)。男性与无进展生存率(60% vs 69%;P<.05)和总生存率(76% vs 89%;P<.05)较差有关。肿瘤位于后颅窝与无进展生存率(59% vs 74%;P<.05)和总生存率(79% vs 89%;P<.01)较差有关。21 名患者(5.4%)需要助听器;其中 13 名接受了顺铂治疗,包括 3 名双侧听力丧失的患者。45 名患者(11.7%)需要激素替代治疗,通常是生长激素(38/45)。2 级+脑干毒性的累积发生率为 4%,发生在接受>54GyRBE 的患者中更为常见。2 名患者(0.5%)死于脑干坏死。第二恶性肿瘤发生率为 0.8%。

结论

质子治疗在没有意外毒性的情况下提供了与现代光子治疗相当的疾病控制。长期生存率高证明了在这一年轻人群中减少辐射暴露的努力是合理的。独立于放射方式,本大系列证实,切除范围是生存的最重要可改变因素。

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