Clinical and molecular markers of long-term survival after oligometastasis-directed stereotactic body radiotherapy (SBRT)

被引:118
作者
Wong, Anthony C. [1 ]
Watson, Sydeaka P. [2 ]
Pitroda, Sean P. [1 ]
Son, Christina H. [1 ]
Das, Lauren C. [1 ]
Stack, Melinda E. [3 ]
Uppal, Abhineet [3 ]
Oshima, Go [3 ]
Khodarev, Nikolai N. [1 ,4 ]
Salama, Joseph K. [5 ]
Weichselbaum, Ralph R. [1 ,4 ]
Chmura, Steven J. [1 ]
机构
[1] Univ Chicago, Dept Radiat & Cellular Oncol, 5758 South Maryland Ave,MC 9006, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Publ Hlth Sci, 5758 South Maryland Ave,MC 9006, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Surg, 5758 South Maryland Ave,MC 9006, Chicago, IL 60637 USA
[4] Univ Chicago, Ludwig Ctr Metastasis Res, 5758 South Maryland Ave,MC 9006, Chicago, IL 60637 USA
[5] Duke Univ, Dept Radiat Oncol, Durham, NC USA
关键词
oligometastases; stereotactic body radiotherapy; microRNA; biomarker; classifier; PHASE I/II TRIAL; RADIATION-THERAPY; LIVER RESECTION; CANCER; LUNG; MIR-449A; METASTASECTOMY; SUPPRESSES; EXPRESSION; TARGETS;
D O I
10.1002/cncr.30058
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDThe selection of patients for oligometastasis-directed ablative therapy remains a challenge. The authors report on clinical and molecular predictors of survival from a stereotactic body radiotherapy (SBRT) dose-escalation trial for oligometastases. METHODSPatients who had from 1 to 5 metastases, a life expectancy of >3 months, and a Karnofsky performance status of >60 received escalating SBRT doses to all known cancer sites. Time to progression, progression-free survival, and overall survival (OS) were calculated at the completion of SBRT, and clinical predictors of OS were modeled. Primary tumor microRNA expression was analyzed to identify molecular predictors of OS. RESULTSSixty-one evaluable patients were enrolled from 2004 to 2009. The median follow-up was 2.3 years for all patients (range, 0.2-9.3 years) and 6.8 years for survivors (range, 2.0-9.3 years). The median, 2-year, and 5-year estimated OS were 2.4 years, 57%, and 32%, respectively. The rate of progression after SBRT was associated with an increased risk of death (hazard ratio [HR], 1.44; 95% confidence interval [CI], 1.24-1.82). The time from initial cancer diagnosis to metastasis (HR, 0.98; 95% CI, 0.98-0.99), the time from metastasis to SBRT (HR, 0.98; 95% CI, 0.98-0.99), and breast cancer histology (HR, 0.12; 95% CI, 0.07-0.37) were significant predictors of OS. In an exploratory analysis, a candidate classifier using expression levels of 3 microRNAs (miR-23b, miR-449a, and miR-449b) predicted survival among 17 patients who had primary tumor microRNA expression data available. CONCLUSIONSA subset of oligometastatic patients achieves long-term survival after metastasis-directed SBRT. Clinical features and primary tumor microRNA expression profiling, if validated in an independent dataset, may help select oligometastatic patients most likely to benefit from metastasis-directed therapy. Cancer 2016;122:2242-50. (c) 2016 American Cancer Society. Predictors of outcomes in oligometastatic patients treated with ablative stereotactic radiotherapy (SBRT) are poorly defined. We report that breast cancer histology and slow progression are associated with longer survival in this long-term update of a prospective SBRT dose escalation trial, and we propose a microRNA classifier that may help select oligometastatic patients with better prognosis.
引用
收藏
页码:2242 / 2250
页数:9
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