A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer

and purpose: This retrospective study aimed to investigate the feasibility of shrinking field radiotherapy during chemoradiotherapy in non-small cell lung cancer (NSCLC). Ninety-seven patients with stage III NSCLC who achieved a good response to chemoradiation were analyzed. Computed tomography was...

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Veröffentlicht in:Oncotarget 2018-02, Vol.9 (15), p.12443-12451
Hauptverfasser: Jiang, Chenxue, Han, Shuiyun, Chen, Wucheng, Ying, Xiaozhen, Wu, He, Zhu, Yaoyao, Shi, Guodong, Sun, Xiaojiang, Xu, Yaping
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Sprache:eng
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Zusammenfassung:and purpose: This retrospective study aimed to investigate the feasibility of shrinking field radiotherapy during chemoradiotherapy in non-small cell lung cancer (NSCLC). Ninety-seven patients with stage III NSCLC who achieved a good response to chemoradiation were analyzed. Computed tomography was performed after 40-50 Gy dose radiation to evaluate curative effect. Patients in the shrinking field group underwent resimulation CT scans and shrinking field radiotherapy. Acute symptomatic irradiation-induced pneumonia (ASIP), progression patterns and survival were assessed. Of the 97 patients who achieved response after a median total dose of 60 Gy, fifty patients received shrinking field radiotherapy. The incidence of acute symptomatic irradiation-induced pneumonia tended to be lower for the shrinking field group (18.0% vs. 23.4%, 0.51). The rate of disease progression was significantly higher in the non-shrinking than shrinking field group (95.7% vs. 66.0%, < 0.001). Compared to the non-shrinking field group, the shrinking field group had similar overall survival (30.0 vs. 30.0 months, 0.58) but significantly better median progression-free survival (14.0 vs. 11.0 months, 0.006). Shrinking field radiotherapy during chemoradiotherapy in stage III non-small cell lung cancer seems safe with acceptable toxicities and relapse, and potentially spares normal tissues and enables dose escalation. Prospective trials are warranted.
ISSN:1949-2553
1949-2553
DOI:10.18632/oncotarget.23849