Department of Radiation Medicine, University of Kentucky, Lexington, Kentucky.
Department of Biostatistics, University of Kentucky, Lexington, Kentucky.
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.
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).
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.
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]).
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.
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)。
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。
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)。
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。