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对于难治性高级别胶质瘤患者,大剂量再程放疗联合贝伐单抗是一种可行的挽救性治疗选择。

Large volume re-irradiation with bevacizumab is a feasible salvage option for patients with refractory high-grade glioma.

作者信息

Back Michael, Gzell Cecelia E, Kastelan Marina, Guo Linxin, Wheeler Helen R

机构信息

Northern Sydney Cancer Centre , Royal North Shore Hospital , Sydney , Australia (M.B., C.G., M.K., L.G., H.W.); Northern Clinical School, Sydney Medical School , University of Sydney , Sydney , Australia (M.B., C.G., H.W.).

出版信息

Neurooncol Pract. 2015 Mar;2(1):48-53. doi: 10.1093/nop/npu031. Epub 2014 Dec 15.

Abstract

BACKGROUND

Clinical studies of re-irradiation (ReRT) for relapsed high-grade glioma (HGG) have generally reported the use of small volume ReRT techniques such as stereotactic radiosurgery in selected patients with isolated focal relapse. This study reports the outcome with large-volume ReRT to manage the more common mescenario of extensive diffuse relapse of HGG.

METHODS

All HGG patients managed with an overlapping second course of radiation therapy (RT) for refractory progression of HGG between October 2009 and April 2013 were included. ReRT was initially used with bevacizumab (BEV), then used when disease was refractory to BEV, and finally used upfront with BEV-naïve patients. Tumor volume (GTV) and specific RT dosimetry factors, including the target volume treated (PTV), and cumulative RT dose maximum (Dmax), were analyzed. Median survival post ReRT was calculated using the Kaplan-Meier method and SPPS v19 software.

RESULTS

Eighteen HGG participants with refractory, bulky contrast-enhancing disease received ReRT. Thirteen participants had a maximum tumor diameter >5 cm, and median GTV was 54 cm. Seven participants had BEV-refractory disease, and 8 participants were BEV naïve. ReRT dose was 35-40 Gy in 15 fractions; median PTV was 133 cm, and median Dmax was 98.2 Gy. Median survival post ReRT for all participants was 8 months (95%CI, 5.8-10.2 months); with 10 months and 3 months for the BEV-naïve and BEV-refractory participants, respectively ( = .024). Two early participants, who were managed without BEV, were later salvaged with BEV, including one who required craniotomy for radiation necrosis at 6 weeks post RT. No other significant morbidity was reported.

CONCLUSION

ReRT combined with BEV is a feasible salvage treatment option for diffuse refractory HGG.

摘要

背景

复发高级别胶质瘤(HGG)再程放疗(ReRT)的临床研究通常报道在部分孤立局灶性复发的选定患者中使用小体积ReRT技术,如立体定向放射外科。本研究报告了大体积ReRT治疗HGG广泛弥漫性复发这一更常见情况的结果。

方法

纳入2009年10月至2013年4月间因HGG难治性进展接受重叠第二程放射治疗(RT)的所有HGG患者。ReRT最初与贝伐单抗(BEV)联合使用,然后在疾病对BEV耐药时使用,最后用于初治未使用BEV的患者。分析肿瘤体积(GTV)和特定的RT剂量学因素,包括治疗的靶体积(PTV)和累积RT剂量最大值(Dmax)。使用Kaplan-Meier方法和SPPS v19软件计算ReRT后的中位生存期。

结果

18例患有难治性、体积较大的强化疾病的HGG参与者接受了ReRT。13例参与者的最大肿瘤直径>5 cm,中位GTV为54 cm。7例参与者患有对BEV耐药的疾病,8例参与者初治未使用BEV。ReRT剂量为35 - 40 Gy,分15次;中位PTV为133 cm,中位Dmax为98.2 Gy。所有参与者ReRT后的中位生存期为8个月(95%CI,5.8 - 10.2个月);初治未使用BEV和对BEV耐药的参与者分别为10个月和3个月(P = 0.024)。两名未使用BEV治疗的早期参与者后来接受了BEV挽救治疗,其中一名在放疗后6周因放射性坏死需要开颅手术。未报告其他严重并发症。

结论

ReRT联合BEV是弥漫性难治性HGG的一种可行挽救治疗选择。

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