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首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Escalated dose for non-small-cell lung cancer with accelerated hypofractionated three-dimensional conformal radiation therapy.
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Escalated dose for non-small-cell lung cancer with accelerated hypofractionated three-dimensional conformal radiation therapy.

机译:非小细胞肺癌的加速剂量及加速的超分割三维共形放射治疗。

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摘要

Background and Purpose: To prospectively assess the feasibility and efficacy of a hypofractionated accelerated radiotherapy regimen (72 Gy in 24 daily fractions, 3Gy per fraction) in patients (pts) with non-resectable non-small-cell lung cancer (NSCLC). Material and Methods: We included 25 pts with a histologically or cytologically proven NSCLC, with KPS>/=70 and <==10% weight loss over prior three months, and with tumour stage I/II medically inoperable (9 pts) or non-resectable stage III a/b without pleural effusion (16 pts). Eleven pts received induction chemotherapy. No more than 30% of the combined lung volume could receive more than 25 Gy and the maximal biological effective dose to the spinal cord was maintained below 44 Gy. Results: No grade-4 acute toxicity event was reported. Two pts had a treatment break because of grade-3 acute oesophagitis. Twenty-two pts were evaluable for long-term toxicity (median follow-up=9.7 months, range 4 to 30.2 months). There were 4 Grade-1 pulmonary and 2 Grade-1oesophageal long-term toxicity events. Twenty-two pts were evaluable for tumour response with 7 complete and 8 partial responses, 5 stable diseases and 2 progressive diseases. The actuarial 1-year overall and thoracic-progression-free survival rates were 68% and 72% respectively. Conclusions: This study demonstrates the feasibility of the experimental radiotherapy schedule, however more data are needed to confirm its efficacy.
机译:背景与目的:前瞻性评估在不可切除的非小细胞肺癌(NSCLC)患者中采用次分割加速放疗方案(24天每天72 Gy,每部分3Gy)的可行性和疗效。材料和方法:我们纳入了25份经组织学或细胞学证实的NSCLC,在过去三个月中KPS> / = 70且体重减轻=== 10%,并且I / II期肿瘤在医学上无法手术(9 pts)或无-可切除的III a / b期,无胸腔积液(16分)。 11例接受诱导化疗。合并肺容积的不超过30%可以接受超过25 Gy,并且对脊髓的最大生物学有效剂量维持在44 Gy以下。结果:未报告4级急性毒性事件。 2名患者因3级急性食管炎而中断治疗。长期毒性评估为22分(中位随访时间为9.7个月,范围4到30.2个月)。发生了4次1级肺部疾病和2次1级食管长期毒性事件。共有22分可评估为肿瘤反应,其中有7种完全反应和8种部分反应,5种稳定疾病和2种进行性疾病。精算1年总生存率和无胸廓无进展生存率分别为68%和72%。结论:这项研究证明了放疗实验的可行性,但是需要更多的数据来证实其疗效。

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