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Ⅱ/Ⅲ期非小细胞肺癌放化疗后残留病变立体定向体部放疗的前瞻性研究更新。

Update of a Prospective Study of Stereotactic Body Radiation Therapy for Post-Chemoradiation Residual Disease in Stage II/III Non-Small Cell Lung Cancer.

机构信息

Department of Radiation Medicine, University of Kentucky, Lexington, Kentucky.

Department of Biostatistics, University of Kentucky, Lexington, Kentucky.

出版信息

Int J Radiat Oncol Biol Phys. 2017 Nov 1;99(3):652-659. doi: 10.1016/j.ijrobp.2017.07.036. Epub 2017 Jul 29.

Abstract

PURPOSE

To report long-term outcomes (risk of late toxicities, local control, and survival) of dose escalation by stereotactic radiation therapy boost to residual fluorodeoxyglucose positron emission tomography-positive residual disease after chemoradiation (CRT) in stage III non-small cell lung cancer (NSCLC).

METHODS AND MATERIALS

Patients with stage IIB/III NSCLC underwent computed tomography or positron emission tomography-computed tomography screening approximately 1 month after completion of CRT. Limited residual disease (≤5 cm) within the site of the primary tumor received a stereotactic radiation therapy boost of either 10 Gy × 2 fractions or 6.5 Gy × 3 fractions to the primary tumor, to achieve a total Biologically Equivalent Dose >100 Gy.

RESULTS

Thirty-seven patients received protocol therapy. With a median follow-up of 25.2 months, the crude local control rate for the entire group was 78% (n=29), but 10 patients (29%) and 24 patients (65%) developed regional and metastatic disease, respectively. At last follow-up, 5 patients (13.5%) remain alive, all with no evidence of disease, whereas 27 (73%) died of disease and the remaining 5 (13.5%) died of other causes. Median overall survival (OS) for the entire group was 25.2 months. Predictors for grade 3 pneumonitis included age and mean lung dose. Poorer median OS was associated with histology: median OS 15.6 months for squamous cell versus 34.8 months for other histologies (large cell neuroendocrine tumors excluded) (P=.04). The median progression-free survival was 6 months, with IIIB disease having significantly worse median progression-free survival (stages IIB/IIA being 9.4 months, vs 4.7 months for stage IIIB [P=.03]).

CONCLUSIONS

Stereotactic radiation therapy boost after CRT is a safe treatment resulting in improvements in local control for locally advanced NSCLC. No additional late toxicities were seen. Possible improvement in OS was found, but further study in a larger prospective trial is needed.

摘要

目的

报告在放化疗(CRT)后,对氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)阳性残留病灶进行立体定向放疗(SRT)加量治疗,以提高 III 期非小细胞肺癌(NSCLC)局部控制率和生存率(晚期毒性、局部控制率和生存率)。

方法和材料

接受过 IIB/III 期 NSCLC 治疗的患者在 CRT 完成后大约 1 个月进行 CT 或 PET-CT 筛查。原发肿瘤部位的局限性残留病灶(≤5cm)接受 SRT 加量治疗,总生物等效剂量(Biologically Equivalent Dose,BED)>100Gy,包括两种剂量分割方式:10Gy×2 分次或 6.5Gy×3 分次。

结果

37 例患者接受了方案治疗。中位随访 25.2 个月,全组的粗局部控制率为 78%(29 例),但有 10 例(29%)和 24 例(65%)患者分别出现区域性和远处转移。最后一次随访时,5 例(13.5%)患者存活且无疾病证据,27 例(73%)死于疾病,其余 5 例(13.5%)死于其他原因。全组的中位总生存(Overall Survival,OS)为 25.2 个月。3 级放射性肺炎的预测因素包括年龄和平均肺剂量。OS 较差的患者与组织学类型有关:鳞癌的中位 OS 为 15.6 个月,其他组织学类型(大细胞神经内分泌肿瘤除外)的中位 OS 为 34.8 个月(P=.04)。中位无进展生存(Progression-Free Survival,PFS)为 6 个月,IIIb 期疾病的中位 PFS 明显更差(IIB/IIA 期为 9.4 个月,IIIb 期为 4.7 个月,P=.03)。

结论

CRT 后行 SRT 加量治疗是一种安全的治疗方法,可提高局部晚期 NSCLC 的局部控制率。未观察到额外的晚期毒性。OS 可能有改善,但需要更大规模前瞻性试验进一步研究。

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