Volume 72, Issue 2 , Pages 404-409, 1 October 2008
Baseline Pulmonary Function as a Predictor for Survival and Decline in Pulmonary Function Over Time in Patients Undergoing Stereotactic Body Radiotherapy for the Treatment of Stage I Non–Small-Cell Lung Cancer
Purpose
To examine the effect of baseline forced expiratory volume in 1 second (FEV1) and diffusion capacity for carbon monoxide (Dlco) on posttreatment survival and pulmonary function decrease after stereotactic body radiotherapy (SBRT) for patients with early-stage non–small-cell lung cancer (NSCLC).
Methods and Materials
Seventy medically inoperable patients with Stage I NSCLC were treated with definitive SBRT to a dose of 6,000 (Stage IA) or 6,600 cGy (Stage IB), given in three equal fractions. Baseline and serial posttreatment pulmonary function data were collected.
Results
Median age was 70.5 years, and median follow-up was 2.17 years. Median pretreatment FEV1 and Dlco were 1.05 L and 10.06 mg/min/mm Hg, respectively. There was no significant decrease in survival in patients with baseline FEV1 and Dlco less than the median value and less than the lowest quartile, whereas patients with values greater than the highest quartile of baseline FEV1 had significantly inferior survival. There was no significant effect of pretreatment FEV1 or Dlco on posttreatment levels. There was a statistically significant decrease in Dlco of 1.11 mg/min/mm Hg/y.
Conclusions
Poor baseline pulmonary function did not predict decreased survival or pulmonary function after treatment. A statistically significant decrease in Dlco after treatment was seen, similar to decreases seen in studies delivering standard thoracic radiotherapy. We conclude that low pretreatment FEV1 and/or Dlco alone should not be used to exclude patients with NSCLC from treatment with SBRT.
Stereotactic body radiotherapy, Non–small-cell lung cancer, Pulmonary function, Toxicity
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Presented in abstract form as an oral presentation at the 48th Annual Meeting of the American Society of Therapeutic Radiology and Oncology (ASTRO), November 5–9, 2006, Philadelphia, PA.
Supported by Grant No. 5R21CA097721-02 from the US National Institutes of Health.
ClinicalTrials.gov identifier: NCT00246181.
Conflict of interest: none.
PII: S0360-3016(08)00045-X
doi:10.1016/j.ijrobp.2007.12.051
© 2008 Elsevier Inc. All rights reserved.
Volume 72, Issue 2 , Pages 404-409, 1 October 2008
