Long term outcome after 48Gy stereotactic ablative body radiotherapy for peripheral stage I non-small cell lung cancer

被引:6
作者
Dubaere, Emilie [1 ]
Goffaux, Mathilde [2 ]
Wanet, Marie [1 ]
Bihin, Benoit [2 ,3 ]
Gheldof, Celine [1 ]
Demoulin, Anne-Sophie [4 ]
Bolly, Antoine [1 ]
Bustin, Frederique [4 ]
Duplaquet, Fabrice [3 ]
Baugnee, Paul-Emile [5 ]
Gustin, Michel [4 ]
Hers, Vincent [5 ]
Maisin, Fabienne [1 ]
Marchand, Eric [2 ,3 ]
Ocak, Sebahat [3 ,8 ]
Pirard, Lionel [3 ]
Vancutsem, Oswald [6 ]
Van Neck, Evelyne [7 ]
Vandermoten, Guy [5 ]
Zaharia, Luminata [5 ]
Remouchamps, Vincent [1 ,2 ]
机构
[1] CHU UCL Namur, Dept Radiotherapy, Site Ste Elisabeth,Pl Louise Godin 15, B-5000 Namur, Belgium
[2] NARILIS, Namur, Belgium
[3] CHU UCL Namur, Site Godinne, Yvoir, Belgium
[4] CHR Citadelle Liege, Liege, Belgium
[5] CHR Sambre & Meuse, Namur, Belgium
[6] Clin St Luc Bouge, Namur, Belgium
[7] CHU UCL Namur, Site Dinant, Dinant, Belgium
[8] UCL, IREC, Pole Pneumol ORL & Dermatol PNEU, Brussels, Belgium
关键词
Stereotactic ablative radiotherapy; Lung cancer; Non-small cell lung cancer; Survival; POSITRON-EMISSION-TOMOGRAPHY; RADIATION-THERAPY; RECURRENCE;
D O I
10.1186/s12885-019-5863-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundTo evaluate the outcome of patients treated with stereotactic ablative body radiotherapy (SABR) with curative intent for stage I non-small cell lung cancer (NSCLC) with regard to local, regional and distant tumor control, disease-free survival (DFS), overall survival (OS) and toxicity.MethodsData of 300 patients treated with SABR for NSCLC cancer for the period of November 2007 to June 2016 were retrospectively analyzed. Of which, 189 patients had single primary lung lesion and were included in the study. The prescribed dose for the tumor was 48Gy, given in 12Gyx4 fractions for all patients. In 2010, an improved protocol was established in advanced technology for the planning CT, dose calculation and imaging. Cumulative incidence function (CIF) of local, regional, distant or any recurrences were computed using competing risk analysis with death as a competing event. Survivals (DFS and OS) were estimated using the Kaplan-Meier method and Cox proportional regression was used for comparisons. Toxicities were graded according to the common terminology criteria for adverse events version 4.0 (CTCAE v.4).ResultsDiagnosis was histologically confirmed in 42% of the patients (N=80). At 1, 2 and 4years, the cumulative incidence function (CIF) of local relapses were 8% [4-13%], 15% [10-21%] and 18% [12-25%], the CIF of regional relapses were 4% [2-8%], 10% [6-16%] and 12% [8-19%], the CIF of distant relapses were 9% [5-14%], 15% [11-22%] and 20% [15-28%] and the CIF of any relapses were 14% [10-20%], 28% [22-36%], 34% [27-43%], respectively. After 1, 2 and 4years, the OS rates were 83% [95% CI: 78-89%] (N=128), 65% [95% CI: 57-73%] (N=78) and 37% [95% CI: 29-47%] (N=53), respectively. The median survival time was 37months. The DFS after 1, 2 and 4years reached 75% [95% CI: 68-81%] (N=114), 49% [95% CI: 42-58%] (N=60) and 31% [95% CI: 24-41%] (N=41), respectively. No grade 4 or 5 toxicity was observed.ConclusionsWe observed a long-term local control and survival after SABR for peripheral stage I NSCLC in this large series of patients with the expected low toxicity.
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页数:8
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