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Accelerated hypofractionated radiation therapy (AHRT) for non-small-cell lung cancer: can we leave standard fractionation?
Rodríguez de Dios, N; Sanz, X; Foro, P; Membrive, I; Reig, A; Ortiz, A; Jiménez, R; Algara, M.
Afiliação
  • Rodríguez de Dios, N; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Sanz, X; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Foro, P; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Membrive, I; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Reig, A; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Ortiz, A; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Jiménez, R; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
  • Algara, M; Hospital de la Esperanza. Department of Radiation Oncology. Barcelona. Spain
Clin. transl. oncol. (Print) ; 19(4): 440-447, abr. 2017. tab, graf
Article em En | IBECS | ID: ibc-160893
Biblioteca responsável: ES1.1
Localização: BNCS
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 (BED10 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 (AU)
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Coleções: 06-national / ES Base de dados: IBECS Assunto principal: Pneumonia / Prognóstico / Radioterapia / Carcinoma Pulmonar de Células não Pequenas / Fracionamento da Dose de Radiação / Tomografia por Emissão de Pósitrons Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Article
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Coleções: 06-national / ES Base de dados: IBECS Assunto principal: Pneumonia / Prognóstico / Radioterapia / Carcinoma Pulmonar de Células não Pequenas / Fracionamento da Dose de Radiação / Tomografia por Emissão de Pósitrons Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Article