The Effect of Biologically Effective Dose and Radiation Treatment Schedule on Overall Survival in Stage I Non-Small Cell Lung Cancer Patients Treated With Stereotactic Body Radiation Therapy.

Stahl, John M; Ross, Rudi; Harder, Eileen M; Mancini, Brandon R; Soulos, Pamela R; Finkelstein, Steven E; Shafman, Timothy D; Dosoretz, Arie P et al. · Int J Radiat Oncol Biol Phys · 2016

retrospective_cohort · Level III

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Abstract

To determine the effect of biologically effective dose (BED<sub>10</sub>) and radiation treatment schedule on overall survival (OS) in patients with early-stage non-small cell lung cancer (NSCLC) undergoing stereotactic body radiation therapy (SBRT). Using data from 65 treatment centers in the United States, we retrospectively reviewed the records of T1-2 N0 NSCLC patients undergoing SBRT alone from 2006 to 2014. Biologically relevant covariates, including dose per fraction, number of fractions, and time between fractions, were used to quantify BED<sub>10</sub> and radiation treatment schedule. The linear-quadratic equation was used to calculate BED<sub>10</sub> and to generate a dichotomous dose variable of <105 Gy versus ≥105 Gy BED<sub>10</sub>. The primary outcome was OS. We used the Kaplan-Meier method, the log-rank test, and Cox proportional hazards regression with propensity score matching to determine whether prescription BED<sub>10</sub> was associated with OS. We identified 747 patients who met inclusion criteria. The median BED<sub>10</sub> was 132 Gy, and 59 (7.7%) had consecutive-day fractions. Median follow-up was 41 months, and 452 patients (60.5%) had died by the conclusion of the study. The 581 patients receiving ≥105 Gy BED<sub>10</sub> had a median survival of 28 months, whereas the 166 patients receiving <105 Gy BED<sub>10</sub> had a median survival of 22 months (log-rank, P=.01). Radiation treatment schedule was not a significant predictor of OS on univariable analysis. After adjusting for T stage, sex, tumor histology, and Eastern Cooperative Oncology Group performance status, BED<sub>10</sub> ≥105 Gy versus <105 Gy remained significantly associated with improved OS (hazard ratio 0.78, 95% confidence interval 0.62-0.98, P=.03). Propensity score matching on imbalanced variables within high- and low-dose cohorts confirmed a survival benefit with higher prescription dose. We found that dose escalation to 105 Gy BED<sub>10</sub> and beyond may improve survival in NSCLC patients treated with SBRT.

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