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ⅠB-ⅢB 期非小细胞肺癌:标准分割剂量≥80Gy 根治性放疗的长期结果。

Non-small cell lung cancer in stages I-IIIB: Long-term results of definitive radiotherapy with doses ≥ 80 Gy in standard fractionation.

机构信息

University Clinic of Radiotherapy and Radiation Oncology and radART - Institute for research and development on Advanced Radiation Technologies, Paracelsus Medical University, Salzburg, Austria.

出版信息

Strahlenther Onkol. 2010 Oct;186(10):551-7. doi: 10.1007/s00066-010-2108-3. Epub 2010 Sep 30.

Abstract

PURPOSE

To investigate therapeutic outcome of dose escalation ≥ 80 Gy in nonresected non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS

124 consecutive patients with histologically/cytologically proven NSCLC were enrolled. Tumor stage I, II, IIIA, and IIIB was diagnosed in 30, eight, 39, and 47 patients, respectively. 38 patients (31%) had weight loss > 5% during the 3 months before diagnosis. A median dose of 88.2 Gy (range 80.0-96.0 Gy), 69.3 Gy (63.0-88.0 Gy) and 56.7 Gy was applied to primary lesions, involved lymph nodes, and elective nodes (within a region of about 6 cm cranial to macroscopically involved nodes), respectively. Daily fractional ICRU doses of 2.0-2.2 Gy were delivered by the conformal target-splitting technique. 58 patients (47%) received induction chemotherapy, in median two cycles prior to radiotherapy.

RESULTS

Median follow-up time of all patients was 19 months, of patients alive 72.4 months (69-121 months). The cumulative actual overall survival rate at 2 and 5 years amounts to 39% and 11.3%, respectively, resulting in a median overall survival time of 19.6 months. According to stages I, II, IIIA, and IIIB, the median overall survival times are 31.8, 31.4, 19.0, and 14.5 months, respectively. The locoregional tumor control rate at 2 years is 49%. Apart from one treatment-related death (pneumonitis), acute toxicity according to EORTC/RTOG scores was moderate: lung grade 2 (n = 7), grade 3 (n = 3); esophagus grade 1 (n = 11); heart grade 3 (n = 1, pericarditis). No late toxicity grade > 1 has been observed.

CONCLUSION

Sequential, conventionally fractionated high-dose radiotherapy by conformal target splitting is well tolerated. The results for survival and locoregional tumor control seem to at least equalize the outcome of simultaneous chemoradiation approaches, which, at present, are considered "state of the art" for patients with nonresected NSCLC. A higher potential of radiation therapy might be reached by accelerated fractionation regimens.

摘要

目的

研究非手术治疗的非小细胞肺癌(NSCLC)中剂量递增≥80Gy 的治疗效果。

方法

纳入 124 例经组织学/细胞学证实的 NSCLC 患者。肿瘤分期为 I 期、II 期、IIIA 期和 IIIB 期的患者分别为 30、8、39 和 47 例。38 例(31%)患者在诊断前 3 个月体重减轻>5%。原发肿瘤、受累淋巴结和选择性淋巴结(位于大体受累淋巴结头侧约 6cm 区域内)的中位剂量分别为 88.2Gy(范围 80.0-96.0Gy)、69.3Gy(63.0-88.0Gy)和 56.7Gy。采用适形靶区分割技术,每日分次 ICRU 剂量为 2.0-2.2Gy。58 例(47%)患者接受了诱导化疗,中位数为放疗前 2 个周期。

结果

所有患者的中位随访时间为 19 个月,存活患者的中位随访时间为 72.4 个月(69-121 个月)。2 年和 5 年的累积实际总生存率分别为 39%和 11.3%,中位总生存时间为 19.6 个月。根据分期 I、II、IIIA 和 IIIB,中位总生存时间分别为 31.8、31.4、19.0 和 14.5 个月。2 年时局部区域肿瘤控制率为 49%。除 1 例与治疗相关的死亡(肺炎)外,EORTC/RTOG 评分的急性毒性为中度:肺 2 级(n=7),3 级(n=3);食管 1 级(n=11);心脏 3 级(n=1,心包炎)。未观察到晚期毒性>1 级。

结论

序贯、常规分割高剂量放疗通过适形靶区分割是可以耐受的。生存和局部区域肿瘤控制的结果至少与同时放化疗方法的结果相当,目前后者被认为是未切除 NSCLC 患者的“标准治疗方法”。通过加速分割方案可能会达到更高的放疗潜力。

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