Fowler J F
Int J Radiat Oncol Biol Phys. 1985 Apr;11(4):665-74. doi: 10.1016/0360-3016(85)90296-2.
In this review the poor clinical gains from hyperbaric oxygen (HBO) and misonidazole (MISO) are discussed critically. The biggest factor reducing clinical gains is almost certainly reoxygenation. Other possible reasons include vasoconstrictive self-limitation of HBO and neurotoxicity of MISO, so that the radiosensitization of any hypoxic cells in human tumors was not adequate. Nevertheless, there have been some positive clinical results, so that hypoxic cells can sometimes be a problem in some tumors, especially those of the head and neck, even after multiple fraction radiotherapy. While hypoxic cell radioresistance is obviously only one form of radioresistance it is a large factor of resistance when hypoxic cells are present. Current developments are briefly reviewed: the 'new' clinical sensitizers Ro-03-8799 and SR-2508 which should be 3 to 10 times more efficient than MISO if viable hypoxic cells are present; and methods of measuring which human tumors might have significant numbers of hypoxic viable cells.
在本综述中,我们批判性地讨论了高压氧(HBO)和米索硝唑(MISO)在临床上的欠佳疗效。几乎可以肯定,导致临床疗效不佳的最大因素是再氧合作用。其他可能的原因包括HBO的血管收缩性自我限制以及MISO的神经毒性,以至于人类肿瘤中任何缺氧细胞的放射增敏作用都不充分。然而,也有一些积极的临床结果,因此即使在多次分割放疗后,缺氧细胞有时在某些肿瘤中,尤其是头颈部肿瘤中,仍是一个问题。虽然缺氧细胞放射抗性显然只是放射抗性的一种形式,但当存在缺氧细胞时,它是抗性的一个重要因素。本文简要综述了当前的进展:“新型”临床增敏剂Ro-03-8799和SR-2508,如果存在存活的缺氧细胞,其效率应比MISO高3至10倍;以及测量哪些人类肿瘤可能含有大量缺氧存活细胞的方法。