Amifostine is a potent radioprotector of salivary glands in radioiodine therapy. Structural and ultrastructural findings.

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Amifostine is a potent radioprotector of salivary glands in radioiodine therapy. Structural and ultrastructural findings. / Kutta, Hannes; Kampen, Uwe; Sagowski, Christoph; Brenner, Winfried; Bohuslavizki, Karl-Heinz; Paulsen, Friedrich.

In: STRAHLENTHER ONKOL, Vol. 181, No. 4, 4, 2005, p. 237-245.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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Kutta H, Kampen U, Sagowski C, Brenner W, Bohuslavizki K-H, Paulsen F. Amifostine is a potent radioprotector of salivary glands in radioiodine therapy. Structural and ultrastructural findings. STRAHLENTHER ONKOL. 2005;181(4):237-245. 4.

Bibtex

@article{490314cf82f74277a15b8a7efb6373e0,
title = "Amifostine is a potent radioprotector of salivary glands in radioiodine therapy. Structural and ultrastructural findings.",
abstract = "BACKGROUND AND PURPOSE: Salivary gland impairment following high-dose radioiodine treatment is well recognized. Since differentiated thyroid cancer has a good prognosis, reduction of long-term side effects is important. This study investigates the radioprotective effects of amifostine in salivary glands of rabbits receiving high-dose radioiodine therapy so as to obtain deeper insight in changes on the cellular and ultrastructural level. MATERIAL AND METHODS: A total of 20 rabbits were investigated. High-dose radioiodine therapy applying 1 GBq (131)I was performed in 16 animals. Eight of these 16 animals received 200 mg/m(2) body surface amifostine prior to high-dose radioiodine therapy. Four additional rabbits served as controls, two receiving amifostine, the other two no treatment at all. Subsequently, salivary glands (submandibular and parotid glands, respectively) of all animals were examined by light and transmission electron microscopy. RESULTS: Parenchymal damage of both parotid and submandibular glands, specially acinar structures comprising cell organelles and nuclei, of animals pretreated with amifostine was much less pronounced than in animals without amifostine pretreatment. CONCLUSION: The results indicate that parenchymal damage in salivary glands induced by high-dose radioiodine therapy can significantly be reduced by amifostine. Therefore, amifostine therapy may increase quality of life in patients with differentiated thyroid cancer after radioiodine treatment.",
author = "Hannes Kutta and Uwe Kampen and Christoph Sagowski and Winfried Brenner and Karl-Heinz Bohuslavizki and Friedrich Paulsen",
year = "2005",
language = "Deutsch",
volume = "181",
pages = "237--245",
journal = "STRAHLENTHER ONKOL",
issn = "0179-7158",
publisher = "Urban und Vogel",
number = "4",

}

RIS

TY - JOUR

T1 - Amifostine is a potent radioprotector of salivary glands in radioiodine therapy. Structural and ultrastructural findings.

AU - Kutta, Hannes

AU - Kampen, Uwe

AU - Sagowski, Christoph

AU - Brenner, Winfried

AU - Bohuslavizki, Karl-Heinz

AU - Paulsen, Friedrich

PY - 2005

Y1 - 2005

N2 - BACKGROUND AND PURPOSE: Salivary gland impairment following high-dose radioiodine treatment is well recognized. Since differentiated thyroid cancer has a good prognosis, reduction of long-term side effects is important. This study investigates the radioprotective effects of amifostine in salivary glands of rabbits receiving high-dose radioiodine therapy so as to obtain deeper insight in changes on the cellular and ultrastructural level. MATERIAL AND METHODS: A total of 20 rabbits were investigated. High-dose radioiodine therapy applying 1 GBq (131)I was performed in 16 animals. Eight of these 16 animals received 200 mg/m(2) body surface amifostine prior to high-dose radioiodine therapy. Four additional rabbits served as controls, two receiving amifostine, the other two no treatment at all. Subsequently, salivary glands (submandibular and parotid glands, respectively) of all animals were examined by light and transmission electron microscopy. RESULTS: Parenchymal damage of both parotid and submandibular glands, specially acinar structures comprising cell organelles and nuclei, of animals pretreated with amifostine was much less pronounced than in animals without amifostine pretreatment. CONCLUSION: The results indicate that parenchymal damage in salivary glands induced by high-dose radioiodine therapy can significantly be reduced by amifostine. Therefore, amifostine therapy may increase quality of life in patients with differentiated thyroid cancer after radioiodine treatment.

AB - BACKGROUND AND PURPOSE: Salivary gland impairment following high-dose radioiodine treatment is well recognized. Since differentiated thyroid cancer has a good prognosis, reduction of long-term side effects is important. This study investigates the radioprotective effects of amifostine in salivary glands of rabbits receiving high-dose radioiodine therapy so as to obtain deeper insight in changes on the cellular and ultrastructural level. MATERIAL AND METHODS: A total of 20 rabbits were investigated. High-dose radioiodine therapy applying 1 GBq (131)I was performed in 16 animals. Eight of these 16 animals received 200 mg/m(2) body surface amifostine prior to high-dose radioiodine therapy. Four additional rabbits served as controls, two receiving amifostine, the other two no treatment at all. Subsequently, salivary glands (submandibular and parotid glands, respectively) of all animals were examined by light and transmission electron microscopy. RESULTS: Parenchymal damage of both parotid and submandibular glands, specially acinar structures comprising cell organelles and nuclei, of animals pretreated with amifostine was much less pronounced than in animals without amifostine pretreatment. CONCLUSION: The results indicate that parenchymal damage in salivary glands induced by high-dose radioiodine therapy can significantly be reduced by amifostine. Therefore, amifostine therapy may increase quality of life in patients with differentiated thyroid cancer after radioiodine treatment.

M3 - SCORING: Zeitschriftenaufsatz

VL - 181

SP - 237

EP - 245

JO - STRAHLENTHER ONKOL

JF - STRAHLENTHER ONKOL

SN - 0179-7158

IS - 4

M1 - 4

ER -