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Long-term follow-up of patients with locally advanced non-small cell lung cancer receiving concurrent hypofractionated chemoradiotherapy with or without cetuximab.

Iris Walraven ,
Michel van den Heuvel ,
Judi van Diessen ,
Eva Schaake ,
Wilma Uyterlinde ,
Joachim Aerts ,
Frederieke Koppe ,
Henk Codrington ,
Peter Kunst ,
Edith Dieleman ,
Paul van de Vaart ,
Marcel Verheij ,
Jose Belderbos

Abstract

MATERIALS AND METHODS

A 2-armed phase II, multi-center study (NTR2230) was performed with the aim to assess the effect of cetuximab to concurrent chemoradiotherapy in LA-NSCLC patients (stage II/IIIA/B). Arm A received high dose radiotherapy (24 × 2.75 Gy) and concurrent daily low-dose cisplatin (6 mg/m(2)). Arm B received an identical treatment regimen with additional weekly cetuximab. Kaplan-Meier survival curves and 1-, 2- and 5-year OS proportions were calculated.

RESULTS

Between February 2009 and May 2011, 102 patients were randomly allocated in two arms. Median OS was 31.5 months (range 12.8-52.3), not significantly different between arms A and B; 33.0 (range 17.0-57.0) and 30.0 (11.0-52.0) months. 1-, 2- and 5-year OS rates were 74.5%, 59.4% and 37.3%, respectively. In multivariate analyses, worse performance score, V35 of the esophagus and the existence of comorbidities were significantly (P-value<0.05) associated with a shorter OS.

BACKGROUND AND PURPOSE

Radiation dose escalation using hypofractionation might improve overall survival (OS). We investigated OS in a phase II multicenter study in locally advanced non-small cell lung cancer (LA-NSCLC) patients treated with hypofractionated concurrent chemoradiotherapy.

DISCUSSION

In this phase II trial, the median OS for the entire group was remarkably high; 31.5 months. Furthermore, 5-year OS was still 37.3%. Hypofractionation might contribute to improved OS in LA-NSCLC patients.

More about this publication

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology

Volume 118
Issue nr. 3
Pages 442-6
Publication date 01-03-2016

Full text links

Publisher website (DOI) 10.1016/j.radonc.2016.02.011
Europe PubMed Central 26900091
Pubmed 26900091

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