首页> 外文期刊>Journal of Cancer Research and Therapeutics >Treatment of high-grade gliomas using escalating doses of hypofractionated simultaneous integrated boost-intensity-modulated radiation therapy in combination with temozolomide: A modified Phase I clinical trial
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Treatment of high-grade gliomas using escalating doses of hypofractionated simultaneous integrated boost-intensity-modulated radiation therapy in combination with temozolomide: A modified Phase I clinical trial

机译:改良剂量的次分割同时增强免疫强度联合放射疗法联合替莫唑胺治疗高级神经胶质瘤:一项改良的I期临床试验

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Background: Recent studies have shown that hypofractionated simultaneous integrated boost-intensity-modulated radiation therapy (SIB-IMRT) provided certain survival benefits over other fractionation methods for high-grade gliomas. However, the best hypofractionation mode and its efficacy have not been confirmed. The purpose of this study was to investigate the maximum tolerated dose (MTD) of hypofractionated SIB-IMRT with stepwise escalating doses combined with temozolomide (TMZ) for treating malignant gliomas. Methods: The patients received concurrent postoperative radiotherapy and chemotherapy. SIB-IMRT was adopted to increase the dose both in the surgical cavity and residual tumor (planning target volume 1). The dose at each fraction was gradually increased from 2.8 Gy/f (total of 20 times), with an escalating dose interval of 0.4 Gy. The planning target volume 2 involved the 2 cm region around surgical cavity, and residual tumor remained unchanged, with 2.5 Gy each time and a total of 50 Gy/20f. TMZ was administered with a dose of 75 mg/m2/day during radiotherapy. Adjuvant TMZ was given at 150–200 mg/m2/day for 5 days every 28 days. A total of 16 patients were enrolled. Results: Three patients exhibited dose-limiting toxicity (DLT), two cases reported Grade 3 headache in the 3.6 Gy/f and 4 Gy/f dose groups, and one patient developed persistent seizures attacks in the 4 Gy/f dose group. Therefore, 4 Gy/f was considered the DLT and the lower dose level of 3.6 Gy/f was regarded as the MTD in the study, with tolerable adverse reactions. The median overall survival (OS) and median progression-free survival (PFS) in this study were 19 and 16 months, respectively. The 1- and 2-year OS and PFS were 86.7%, 31.0% and 73.7%, 26.7%, respectively. Conclusions: It showed that the treatment of high-grade gliomas with hypofractionated SIB-IMRT combined with TMZ had an MTD of 3.6 Gy/f (72 Gy/20f). In addition, the results preliminarily showed improved survival.
机译:背景:最近的研究表明,对于高级神经胶质瘤,超分割同时联合增强强度调制放射治疗(SIB-IMRT)与其他分割方法相比,具有一定的生存优势。但是,最好的分割方法及其功效尚未得到证实。这项研究的目的是研究分次递增剂量联合替莫唑胺(TMZ)治疗恶性神经胶质瘤的次分级SIB-IMRT的最大耐受剂量(MTD)。方法:患者同时接受术后放,化疗。采用SIB-IMRT来增加手术腔和残留肿瘤中的剂量(计划目标体积1)。每个部分的剂量从2.8 Gy / f(共20次)逐渐增加,剂量间隔逐渐增加到0.4 Gy。计划目标体积2涉及手术腔周围2 cm区域,残留肿瘤保持不变,每次为2.5 Gy,总计为50 Gy / 20f。在放疗期间,TMZ的剂量为75 mg / m2 /天。每28天给予150-200 mg / m2 /天的佐剂TMZ,共5天。总共招募了16名患者。结果:3例患者表现出剂量限制性毒性(DLT),在3.6 Gy / f和4 Gy / f剂量组中有2例报告了3级头痛,在4 Gy / f剂量组中有1例患者持续发作。因此,在研究中将4 Gy / f视为DLT,将较低剂量水平3.6 Gy / f视为MTD,且不良反应可忍受。这项研究的中位总体生存期(OS)和无进展生存期(PFS)分别为19个月和16个月。 1年和2年OS和PFS分别为86.7%,31.0%和73.7%,26.7%。结论:研究表明,超低级SIB-IMRT联合TMZ治疗高级别胶质瘤的MTD为3.6 Gy / f(72 Gy / 20f)。此外,结果初步显示存活率提高。

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