Wollner I, Knutsen C, Smith P, Prieskorn D, Chrisp C, Andrews J, Juni J, Warber S, Klevering J, Crudup J
Department of Internal Medicine, University of Michigan Medical School, Ann Arbor.
Cancer. 1988 Apr 1;61(7):1336-44. doi: 10.1002/1097-0142(19880401)61:7<1336::aid-cncr2820610711>3.0.co;2-k.
A 22-micron glass microsphere called TheraSphere (Theragenics Corp., Atlanta, GA) has been developed in which yttrium 89 oxide is incorporated into the glass matrix and is activated by neutron bombardment to form the beta-emitting isotope yttrium 90 (Y 90) before using the spheres as radiotherapeutic vehicles. The injection of up to 12 times (on a liver weight basis) the anticipated human dose of nonradioactive TheraSphere into the hepatic arteries of dogs was well tolerated and produced clinically silent alterations within centrolobular areas. The hepatic arterial (HA) injection of radioactive TheraSphere also produced portal changes similar to those observed in humans after external beam therapy. While the extent of damage increased with the delivered dose, radiation exposures in excess of 30,000 cGy did not cause total hepatic necrosis and were compatible with survival. No microspheres distributed to the bone marrow and absolutely no myelosuppression was encountered in any animal. Proposed hepatic exposures to humans of 5000 to 10,000 cGy by means of these microspheres, therefore, would appear to be feasible and tolerable. Radiotherapeutic microsphere administration preceded by regional infusion of a radiosensitizing agent and/or immediately following the redistribution of blood flow toward intrahepatic tumor by vasoactive agents can potentially yield a synergistic, highly selective attack on tumors confined to the liver.
一种名为TheraSphere(Theragenics公司,佐治亚州亚特兰大)的22微米玻璃微球已被研发出来,其中氧化钇89被掺入玻璃基质中,并通过中子轰击激活,在将这些微球用作放射治疗载体之前形成发射β射线的同位素钇90(Y90)。向狗的肝动脉注射高达预期人类剂量12倍(以肝脏重量计)的非放射性TheraSphere,耐受性良好,且在小叶中心区域产生临床上无症状的改变。放射性TheraSphere的肝动脉(HA)注射也产生了与人类在体外照射后观察到的类似的门静脉变化。虽然损伤程度随给药剂量增加,但超过30,000 cGy的辐射暴露并未导致全肝坏死,且与存活情况相符。没有微球分布到骨髓,并且在任何动物中都未遇到绝对的骨髓抑制。因此,通过这些微球对人类进行5000至10,000 cGy的肝脏照射似乎是可行且可耐受的。在放射治疗微球给药之前进行放射增敏剂的区域灌注和/或在血管活性药物使血流重新分布至肝内肿瘤之后立即给药,可能会对局限于肝脏的肿瘤产生协同、高度选择性的攻击。