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Prediction of radiation-induced liver disease by Lyman normal-tissue complication probability model in three-dimensional conformal radiation therapy for primary liver carcinoma.

PURPOSE: To describe the probability of RILD by application of the Lyman-Kutcher-Burman normal-tissue complication (NTCP) model for primary liver carcinoma (PLC) treated with hypofractionated three-dimensional conformal radiotherapy (3D-CRT). METHODS AND MATERIALS: A total of 109 PLC patients treated by 3D-CRT were followed for RILD. Of these patients, 93 were in liver cirrhosis of Child-Pugh Grade A, and 16 were in Child-Pugh Grade B. The Michigan NTCP model was used to predict the probability of RILD, and then the modified Lyman NTCP model was generated for Child-Pugh A and Child-Pugh B patients by maximum-likelihood analysis. RESULTS: Of all patients, 17 developed RILD in which 8 were of Child-Pugh Grade A, and 9 were of Child-Pugh Grade B. The prediction of RILD by the Michigan model was underestimated for PLC patients. The modified n, m, TD50 (1) were 1.1, 0.28, and 40.5 Gy and 0.7, 0.43, and 23 Gy for patients with Child-Pugh A and B, respectively, which yielded better estimations of RILD probability. The hepatic tolerable doses (TD5) would be MDTNL of 21 Gy and 6 Gy, respectively, for Child-Pugh A and B patients. CONCLUSIONS: The Michigan model was probably not fit to predict RILD in PLC patients. A modified Lyman NTCP model for RILD was recommended.

Adult↗

The effect of ionizing radiation on phagocytosis and the bactericidal power of the blood. II. The effect of radiation on ingestion and digestion of bacteria.

Rats irradiated with 600 r (total body) showed increased indices of both opsonophagic and surface phagocytosis 2, 12, and 24 hours after irradiation. The indices decreased 72 hours after exposure and returned to normal by the 4th to 5th postirradiation day. Bactericidal power of the blood of irradiated animals was depressed when measured 3 and 6 days after exposure to x-rays. Decomplemented serum from irradiated animals was more bactericidal against M. aureus than decomplemented serum from the control rats. This bactericidal substance was destroyed at 78 degrees C. and was found not to require any complement or specific antibodies for action. Extracts of leucocytes from animals 3 days after irradiation demonstrated no bactericidal activity against M. aureus, while extracts from the control animals or rats 1 day after irradiation were actively bactericidal. The extracts from leucocytes of non-irradiated animals were thermolabile, non-dialyzable, had a pH optimum of 7.5, and were capable of being precipitated by NH(4)SO(4) and of calcium phosphate fractionation. The observed increase in susceptibility of irradiated rats to infection with M. aureus was correlated not only with granulopenia but also with the alteration of the above indicated functions of the granulocytes of the irradiated animals.

Animals↗

N-acyl dehydroalanines protect from radiation toxicity and inhibit radiation carcinogenesis in mice.

N-Acyl dehydroalanines have shown free radical scavenging activity. They react with and scavenge mainly oxygen-derived free radicals such as the superoxide anion (O2-.) and the hydroxyl radical (HO.). Ortho-methoxyphenylacetyl dehydroalanine (AD-20) protects total-body irradiated mice against the toxicity induced by X-rays when delivered as a single dose of 700 rads in a short period of time. This degree of protection was of the same order of magnitude as that obtained with the aminothiol S-2-(3-aminopropylamino)-ethylphosphorothioic acid (WR-2721). The radioprotection of AD-20 is extended to all other doses of X-rays tested (from 600 to 800 rads). Furthermore, AD-20 inhibits the development of thymic lymphomas in C57Bl/Ka mice undergoing a leukaemogenic course of irradiation (4 x 175 rads applied at weekly intervals). We postulate that AD-20 may act as a radioprotector and anticarcinogenic agent, most probably by inactivating the oxygen-derived free radicals formed during water radiolysis.

Alanine↗