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Accelerated hypofractionated radiation therapy (AHRT) for non-small-cell lung cancer: can we leave standard fractionation?

Authors :
Dios, N.
Sanz, X.
Foro, P.
Membrive, I.
Reig, A.
Ortiz, A.
Jiménez, R.
Algara, M.
Source :
Clinical & Translational Oncology; Apr2017, Vol. 19 Issue 4, p440-447, 8p
Publication Year :
2017

Abstract

Purpose: To report interim results from a single-institution study conducted to assess accelerated hypofractionated radiotherapy (AHRT) delivered with 3D conformal radiotherapy in two groups of patients with non-small cell lung cancer: (1) patients with early stage disease unable to tolerate surgery and ineligible for stereotactic body radiation therapy, and (2) patients with locally advanced disease unsuitable for concurrent chemoradiotherapy. Methods/patients: A total of 83 patients (51 stage I-II, 32 stage III) were included. Radiotherapy targets included the primary tumor and positive mediastinal areas identified on the pre-treatment PET-CT. Mean age was 77.8 ± 7.8 years. ECOG performance status (PS) was ≥2 in 50.6 % of cases. Radiotherapy was delivered in daily fractions of 2.75 Gy to a total dose of 66 Gy (BED 84 Gy). Acute and late toxicities were evaluated according to NCI CTC criteria. Results: At a median follow-up of 42 months, median overall survival (OS) and cause-specific survival (CSS) were 23 and 36 months, respectively. On the multivariate analysis, PS [HR 4.14, p = 0.0001)], stage [HR 2.51, p = 0.005)], and maximum standardized uptake values (SUVmax) [HR 1.04, p = 0.04)] were independent risk factors for OS. PS [HR 5.2, p = 0.0001)] and stage [HR 6.3, p = 0.0001)] were also associated with CSS. No cases of severe acute or late treatment-related toxicities were observed. Conclusions: OS and CSS rates in patients treated with AHRT for stage I-II and stage III NSCLC were good. Treatment was well tolerated with no grade three or higher treatment-related toxicity. PS, stage, and SUV max were predictive for OS and CSS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1699048X
Volume :
19
Issue :
4
Database :
Complementary Index
Journal :
Clinical & Translational Oncology
Publication Type :
Academic Journal
Accession number :
121741809
Full Text :
https://doi.org/10.1007/s12094-016-1544-7