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采用基于放射生物学方案的立体定向体部放疗治疗Ⅰ期非小细胞肺癌:5 年成熟结果。

Stereotactic body radiotherapy using a radiobiology-based regimen for stage I non-small-cell lung cancer: five-year mature results.

机构信息

*Department of Radiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan; †Radiosurgery Center, Nagoya Kyoritu Hospital, Nagoya, Japan; ‡Department of Radiology, Nagoya Daini Red Cross Hospital, Nagoya, Japan; and §Department of Radiology, Aichi Cancer Center Aichi Hospital, Okazaki, Japan.

出版信息

J Thorac Oncol. 2015 Jun;10(6):960-4. doi: 10.1097/JTO.0000000000000525.

Abstract

INTRODUCTION

Although the protocol of 48 Gy in four fractions over 4 days has been most often employed in stereotactic body radiotherapy (SBRT) for stage I non-small-cell lung cancer in Japan, higher doses are necessary to control larger tumors, and interfraction intervals should be longer than 24 hours to take advantage of reoxygenation. We report the final results of our study testing the following regimen: for tumors less than 1.5, 1.5-3, and greater than 3 cm in diameter, 44, 48, and 52 Gy, respectively, were given in four fractions with interfraction intervals of greater than or equal to 3 days.

METHODS

Among 180 histologically proven patients entered, 120 were medically inoperable and 60 were operable. The median patient age was 77 years (range, 29-89). SBRT was performed with 6-MV photons using four noncoplanar and three coplanar beams. Isocenter doses of 44, 48, and 52 Gy were given to four, 124, and 52 patients, respectively.

RESULTS

The 5-year overall survival rate was 52.2% for all 180 patients and 66% for 60 operable patients. The 5-year local control rate was 86% for tumors less than or equal to 3 cm (44/48 Gy) and 73% for tumors greater than 3 cm (52 Gy; p = 0.076). Grade greater than or equal to 2 radiation pneumonitis developed in 13% (10% for the 44/48-Gy group and 21% for the 52-Gy group; p = 0.056). Other grade 2 toxicities were all less than 4%.

CONCLUSIONS

Our first prospective SBRT study yielded reasonable local control and overall survival rates and acceptable toxicity. Refinement of the protocol including dose escalation may lead to better outcome.

摘要

介绍

尽管在日本,立体定向体部放射治疗(SBRT)治疗 I 期非小细胞肺癌时,最常采用 48 Gy 分 4 次、4 天完成的方案,但为了控制较大肿瘤,需要更高的剂量,并且分次间隔应大于 24 小时,以利用再氧合作用。我们报告了我们的研究结果,该研究测试了以下方案:肿瘤直径小于 1.5cm、1.5-3cm 和大于 3cm 的患者,分别给予 44Gy、48Gy 和 52Gy 的 4 次分割,分次间隔大于或等于 3 天。

方法

在 180 名经组织学证实的患者中,120 名患者因医学原因无法手术,60 名患者可手术。中位患者年龄为 77 岁(范围 29-89 岁)。SBRT 采用 6-MV 光子,使用 4 个非共面和 3 个共面射束进行。44Gy、48Gy 和 52Gy 的等中心点剂量分别给予 4 例、124 例和 52 例患者。

结果

所有 180 例患者的 5 年总生存率为 52.2%,60 例可手术患者的 5 年总生存率为 66%。肿瘤直径小于或等于 3cm(44/48Gy)的患者 5 年局部控制率为 86%,肿瘤直径大于 3cm(52Gy)的患者 5 年局部控制率为 73%(p=0.076)。≥2 级放射性肺炎发生率为 13%(44/48Gy 组 10%,52Gy 组 21%;p=0.056)。其他 2 级毒性均小于 4%。

结论

我们的第一项前瞻性 SBRT 研究取得了合理的局部控制率和总生存率,且毒性可接受。方案的细化包括剂量升级可能会带来更好的结果。

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