Cancer immunotherapy, especially immune-checkpoint inhibitors (ICIs), has paved a new way for the treatment of many types of malignancies, particularly advanced-stage cancers. Accumulating evidence suggests that as a molecular imaging modality, positron emission tomography/computed tomography (PET/CT) can play a vital role in the management of ICIs therapy by using different molecular probes and metabolic parameters. In this review, we will provide a comprehensive overview of the clinical data to support the importance of ¹⁸F-fluorodeoxyglucose PET/CT (¹⁸F-FDG PET/CT) imaging in the treatment of ICIs, including the evaluation of the tumor microenvironment, discovery of immune-related adverse events, evaluation of therapeutic efficacy, and prediction of therapeutic prognosis. We also discuss perspectives on the development direction of ¹⁸F-FDG PET/CT imaging, with a particular emphasis on possible challenges in the future. In addition, we summarize the researches on novel PET molecular probes that are expected to potentially promote the precise application of ICIs.

To investigate the effects of preexisting flaws with different geometries, including flaw inclination angle and ligament angle on dynamic strength, deformation properties, and fracture evolution of rock materials, a series of dynamic impact tests were conducted on green sandstone specimens containing double elliptical flaws using a 75 mm diameter split Hopkinson pressure bar (SHPB) testing device with a high‐speed camera recording in real time. The experimental results show that dynamic strength of specimens with different flaw angles is reduced between 5.91% and 39.92% but from 18.50% to 28.44% for specimens with different ligament angles, indicating that the effect of the flaw angle on the dynamic strength is more significant than that of the ligament angle. However, the dynamic deformation properties are influenced greatly by the ligament angle. Macroscale cracks mostly initiate at or near the flaw tips and then propagate in different paths with varying flaw geometries, leading to the ultimate failure in five typical modes based on the crack coalescence. Shear crack coalescence and tensile crack coalescence are identified through both macroscopic fracturing photos taken by the high‐speed camera and microscopic surface morphology obtained by the scanning electron microscope (SEM).