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Journal Thoracic Oncology

WCLC2016-Abstract-Book_vF-WEB_revNov17-1

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Abstracts <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017<br />

with histologically confirmed, 18 F-fluorodeoxyglucose ( 18 F-FDG)-PET<br />

staged, recurrent or multiple primary NSCLC, suitable for SABR (<br />

62 Gy, respectively (p=.037) (Fig.1). 5-years survival was 19.1% and 29.3% for<br />

treatment with ≤ 62 Gy and > 62 Gy. Conclusion: RT dose may be an important<br />

factor for outcome of patients with LA-NSCLC. Our analysis confirms the<br />

importance of RT dose on outcome in patients with LA NSCLC, but since small<br />

number of patients were included, no firm conclusion could be made and<br />

further clinical investigation is warranted.<br />

Keywords: Locally advanced NSCLC, dose of radiotherapy<br />

POSTER SESSION 2 – P2.05: RADIOTHERAPY<br />

CLINICAL OUTCOME –<br />

TUESDAY, DECEMBER 6, 2016<br />

P2.05-017 TUMOR REGRESSION GRADIENT PREDICTS DISEASE<br />

FREE SURVIVAL<br />

Patrick Berkovic 1 , Leen Paelinck 2 , Katrien Vandecasteele 2 , Akos Gulyban 1 ,<br />

Carlos De Wagter 2 , Bruno Goddeeris 2 , Yolande Lievens 3<br />

1 Liège University Hospital, Liege/Belgium, 2 Ghent University Hospital, Ghent/<br />

Belgium, 3 Radiation <strong>Oncology</strong> Department, Ghent University Hospital, Ghent/<br />

Belgium<br />

Background: Tumor regression during chemoradiation (CRT) in stage III<br />

non-small cell lung cancer patients has been described. Our aim was to<br />

investigate whether the extent of the primary tumor shrinkage is associated<br />

with local control and survival. Methods: Changes in the volume of the<br />

primary tumor (GTV-T) of 41 patients treated with concurrent (cCRT) (n = 21) or<br />

sequential (sCRT) (n=20) CRT were analyzed using cone-beam CT (CBCT) at<br />

every fifth fraction (F5–F30). Only changes in the primary tumor (excluding<br />

the lymph nodes) were considered. Previous research revealed F15 and F20 as<br />

optimal timing for treatment adaptation for cCRT and sCRT respectively<br />

(Berkovic et al. Acta Oncol 2015). Local control and survival data were<br />

reviewed retrospectively. Impact of the tumor regression at the time of the<br />

optimal adaptation timing during treatment (higher or lower than median)<br />

and chemotherapy schedule (cCRT vs. sCRT) on local control and survival were<br />

evaluated using the Kaplan-Meier survival comparison (log-rank test, p

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