Literature DB >> 9463561

[The inhalation versus systemic prevention of pneumonitis during thoracic irradiation].

J Pagel1, M Mohorn, K H Kloetzer, M Fleck, T G Wendt.   

Abstract

BACKGROUND: Pneumonitis is a typical subacute reaction of healthy bronchial tissue to thoracic irradiation. The purpose of the present trial was to show whether prophylactic application of steroids in the course of and following radiotherapy would reduce the incidence of pneumonitis. PATIENTS AND METHODS: Fifty-seven patients receiving thoracic irradiation for bronchial carcinoma were assigned to 2 therapeutic groups; half of the patients were given 10 mg of oral prednisolone per day, while the other half received daily inhalative beclomethasone. All patients were evaluated for radiographic signs of pneumonitis. Thirty-two patients received additional investigations for pulmonary diffusion capacity of carbon monoxide.
RESULTS: The overall incidence of pneumonitis was 17.6% (10/57 patients). Neither total radiation dose nor mode of fractionation did significantly contribute to the incidence of pneumonitis. Those patients showing a pulmonary diffusion capacity for carbon monoxide of less than 60% prior to radiotherapy had a significantly higher risk of developing pneumonitis (4/7) than patients with a higher diffusion capacity (3/25, p = 0.026). In follow-up period we did not see significant changes in diffusion capacity neither with patients who developed pneumonitis nor with those patients showing no evidence of pulmonary injury. Comparing the chest X-ray there were less radiographic changes consistent with pneumonitis in the inhalative beclomethasone (2/28) than in the oral prednisolone group (8/29, p = 0.045). DISCUSSION: In order to reduce the incidence of pneumonitis in patients receiving thoracic irradiation we support a continuous application of steroids in the course of and following radiotherapy. The inhalative use of beclomethasone has proved to be superior to oral prednisolone due to better local efficacy and decreased unwanted side effects.

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Year:  1998        PMID: 9463561     DOI: 10.1007/bf03038224

Source DB:  PubMed          Journal:  Strahlenther Onkol        ISSN: 0179-7158            Impact factor:   3.621


  21 in total

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  5 in total

1.  Elevation in exhaled nitric oxide predicts for radiation pneumonitis.

Authors:  Thomas Guerrero; Josue Martinez; Matthew R McCurdy; Michael Wolski; Mary Francis McAleer
Journal:  Int J Radiat Oncol Biol Phys       Date:  2011-03-04       Impact factor: 7.038

2.  Post-radiotherapy maintenance treatment with fluticasone propionate and salmeterol for lung cancer patients with grade III radiation pneumonitis: A case report.

Authors:  Pingping Zhang; Hongxia Yan; Sheng Wang; Jindan Kai; Guoliang Pi; Yi Peng; Xiyou Liu; Junwei Sun
Journal:  Medicine (Baltimore)       Date:  2018-05       Impact factor: 1.889

3.  Inhalative steroids as an individual treatment in symptomatic lung cancer patients with radiation pneumonitis grade II after radiotherapy - a single-centre experience.

Authors:  C Henkenberens; S Janssen; M Lavae-Mokhtari; K Leni; A Meyer; H Christiansen; M Bremer; N Dickgreber
Journal:  Radiat Oncol       Date:  2016-02-02       Impact factor: 3.481

4.  Radiation pneumonitis in lung cancer patients treated with chemoradiation plus durvalumab.

Authors:  Narek Shaverdian; Maria Thor; Annemarie F Shepherd; Michael D Offin; Andrew Jackson; Abraham J Wu; Daphna Y Gelblum; Ellen D Yorke; Charles B Simone; Jamie E Chaft; Matthew D Hellmann; Daniel R Gomez; Andreas Rimner; Joseph O Deasy
Journal:  Cancer Med       Date:  2020-05-06       Impact factor: 4.452

Review 5.  Radiation-induced lung toxicity - cellular and molecular mechanisms of pathogenesis, management, and literature review.

Authors:  Lukas Käsmann; Alexander Dietrich; Claudia A Staab-Weijnitz; Farkhad Manapov; Jürgen Behr; Andreas Rimner; Branislav Jeremic; Suresh Senan; Dirk De Ruysscher; Kirsten Lauber; Claus Belka
Journal:  Radiat Oncol       Date:  2020-09-10       Impact factor: 3.481

  5 in total

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