Stereotactic body radiation therapy for isolated hilar and mediastinal non-small cell lung cancers

被引:32
|
作者
Horne, Zachary D. [1 ]
Richman, Adam H. [1 ]
Dohopolski, Michael J. [1 ]
Clump, David A. [1 ]
Burton, Steven A. [1 ]
Heron, Dwight E. [1 ]
机构
[1] Univ Pittsburgh, Dept Radiat Oncol, Inst Canc, Pittsburgh, PA USA
关键词
EARLY-STAGE; PHASE-II; TUMORS; TOXICITY; TRIAL; SBRT;
D O I
10.1016/j.lungcan.2017.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: The seminal phase II trial for pulmonary stereotactic body radiation therapy (SBRT) suggested that SORT to central lesions resulted in unacceptable toxicity. Alternative dose-fractionation schemes have been proposed which may improve safety without compromise of efficacy. We report our institutional outcomes of SORT for hilar/mediastinal non-small cell lung cancer (NSCLC). Materials and methods: A retrospective review was conducted of patients with NSCLC in a hilar or mediastinal nodal station which was treated with SBRT. Patients presented with a lesion involving the hilum or mediastinum from primary or oligorecurrent NSCLC. Kaplan-Meier with log-rank testing and Cox analysis were utilized for outcomes analysis. Results: From 2008-2015, 40 patients with median age of 70 were treated with SBRT for primary/oligorecurrent hilar/mediastinal NSCLC with median follow-up of 16.4 months. 85% presented with oligorecurrent disease at a median of 22.4 months following definitive therapy. The aortico-pulmonary window was the target in 40%, the hilum in 25%, lower paratracheal in 20%, subcarinal in 10%, and prevascular in 5%. The median dose was 48 Gy in 4 fractions (range: 35-48 Gy in 4-5 fractions). Median overall (OS) and progression-free (PFS) survivals were 22.7 and 13.1 months, respectively. Two-year local control was 87.7% and not significantly different between hilar and mediastinal targets. Median PFS was significantly improved in patients with hilar vs mediastinal nodal targets: 33.3 vs 8.4 months, respectively (p = 0.031). OS was not statistically different between hilar and mediastinal targets (p = 0.359). On multi variable analysis, hilar vs mediastinal target predicted for PFS (HR 3.045 95%CI [1.044-8.833], p = 0.042), as did shorter time to presentation in patients with oligorecurrence (HR 0.983 [95%CI 0.967-1.000], p = 0.049). Acute grade 3+ morbidity was seen in 3 patients (hemoptysis, pericardial/pleural effusion, heart failure) and late grade 3+ morbidity (hemoptysis) in 1 patient. Conclusion: Hilar/mediastinal SBRT appears to be a safe technique for the local control of isolated nodal disease with limited toxicity from the fractionation schemes utilized.
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页码:1 / 4
页数:4
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