Author/Authors :
Yavas, G Department of Radiation Oncology - Selcuk University, Konya, Turkey , Yavas, C Department of Radiation Oncology - Selcuk University, Konya, Turkey , Celik, E Department of Pathology - Selcuk University, Konya, Turkey , Sen, E Department of Medical Oncology - Selcuk University, Konya, Turkey , Ata, O Department of Medical Oncology - Selcuk University, Konya, Turkey , Afsar, R.E Department of Nephrology - Selcuk University, Konya, Turkey
Abstract :
Background: To evaluate impact of spironolactone (S) on pulmonary toxicity of
concomitant use of thoracic radiotherapy (RT) and trastuzumab (T). Materials and
Methods: Eighty rats were divided into eight groups: group (G) 1 was control
group; G2, G3 and G4 were RT, S and T groups; G5, G6, G7 and G8 were RT+T, T+S,
RT+S and RT+T+S groups respectively. Rats were sacrificed at 6 hour, 21 and 100
day after RT and lung samples were retrieved. Results: By 100th days of RT
inflammation score, lung fibrosis score and TGF- expression were significantly
different within study groups (p values were 0.002, 0.001 and 0.043
respectively). Inflammation score of G8 was significantly lower than
inflammation scores of G2 and G5 (p values: G2-G8= 0.004, and G5-
G8=0.022). Inflammation score of G2 was significantly higher than G7
(p=0.028). There were significant differences regarding to fibrosis scores
between G2-G8 (p=0.015), G2-G7 (p=0.017) and G5-G8 (p=0.011). TGF-β
expression was higher in both G2 and G5 when compared to G8 (p = 0.038).
Conclusion: Our results suggested that S is an effective treatment option for
improving radiation-induced pulmonary fibrosis. These findings should be clarified
with further preclinical and clinical studies.
Keywords :
Trastuzumab , spironolactone , radiotherapy , pulmonary fibrosis , Aldosterone