“…Hypoxia presents in almost all solid tumors and is both an important factor driving tumor progression and a leading obstacle to therapeutic efforts. − Oxygen insufficiency significantly inhibits the generation of appreciable amounts of ROS, leading to a failure to destroy tumor tissues. Meanwhile, previous studies have reported that PDT-mediated oxygen consumption can further increase hypoxic degree, leading to additional adverse consequences such as recurrence or metastasis. − Clinically, researchers have found that hypoxic tumor cells cannot be effectively killed by radiotherapy due to the fact that normal RT is also obviously affected by the amount of O 2 to ensure maximum cell death, namely, the hypoxia due to the consumption of O 2 decreases cellular radiosensitivity and thus fails to “fix” DNA damage during RT. , Feasible strategies to overcome these limitations include delivery of oxygen to tumors, development of oxygen-generating manganese dioxide nanoparticles, or incorporation of antiangiogenesis therapy . Recently, with rapid developments in X-PDT, the issue of hypoxia has also been discussed in this field, with strategies including employment of X-ray excited type-I PDT, NO generation, and oncolytic bacterium therapy proposed to conquer tumor hypoxia and achieve low-dose X-PDT.…”