Abstract
ObjectiveTo develop and validate a new strategy based on radiomics features extracted from intra- and peritumoral regions on CT images for the prediction of atypical responses to the immune checkpoint inhibitor (ICI) in cancer patients.MethodsIn total, 135 patients derived from five hospitals with pathologically confirmed malignancies receiving ICI were included in this retrospective study. Atypical responses including pseudoprogression (PsP) and hyperprogression disease (HPD) were identified as their definitions. A subgroup of standard progression disease (sPD) in 2018 was also involved in this study. Based on pretreatment CT imaging, a total of 107 features were extracted from intra- and peri-tumoral regions, respectively. The least absolute shrinkage and selection operator (Lasso) algorithm was used for feature selection, and multivariate logistic analysis was used to develop radiomics signature (RS). Finally, a total of nine RSs, derived from intra-tumoral, peri-tumoral, and combination of both regions, were built respectively to distinguish PsP vs. HPD, PsP vs. sPD, and HPD vs. sPD. The performance of the RSs was evaluated with discrimination, calibration, and clinical usefulness.ResultsNo significant difference was found when compared in terms of clinical characteristics of PsP, HPD, and sPD. RS based on combined regions outperformed those from either intra-tumoral or peri-tumoral alone, yielding an AUC (accuracy) of 0.834 (0.827) for PsP vs. HPD, 0.923 (0.868) for PsP vs. sPD, and 0.959 (0.894) for HPD vs. sPD in the training datasets, and 0.835 (0.794) for PsP vs. HPD, 0.919 (0.867) for PsP vs. sPD, and 0.933 (0.842) for HPD vs. sPD in the testing datasets. The combined RS showed good fitness (Hosmer–Lemeshow test p > 0.05) and provided more net benefit than the treat-none or treat-all scheme by decision curve analysis in both training and testing datasets.ConclusionPretreatment radiomics are helpful to predict atypical responses to ICI across tumor types. The combined RS outperformed those from either intra- or peri-tumoral alone which may provide a more comprehensive characterization of atypical responses to ICI.
Highlights
The novel development of the immune checkpoint inhibitor (ICI) is approved in a variety of solid tumors, including melanoma, non-small cell lung cancer (NSCLC), and urothelial and microsatellite instability-high (MSI) cancer, represented by programmed cell death-1 (PD-1) and programmed cell death ligand-1 (PD-L1), which became a crucial therapeutic option to improve prognosis [1]
We aim to evaluate the predictive value of radiomics, including intra- and peri-tumoral features that distinguish among PsP, hyperprogression disease (HPD), and standard progression disease (sPD) patients, which may assist clinicians in the precision management of personalized immunotherapy
We investigated the ability of pretreatment CT-based radiomics signatures (RSs) extracted from intra- and peritumoral regions to predict atypical responses to ICI in multiple solid tumors
Summary
The novel development of the immune checkpoint inhibitor (ICI) is approved in a variety of solid tumors, including melanoma, non-small cell lung cancer (NSCLC), and urothelial and microsatellite instability-high (MSI) cancer, represented by programmed cell death-1 (PD-1) and programmed cell death ligand-1 (PD-L1), which became a crucial therapeutic option to improve prognosis [1]. Unlike chemotherapy and tyrosine kinase inhibitor (TKI), ICI plays an antitumor role by blocking the immune checkpoint and enhancing the activity of autologous T cells [2] These effects occur through the restart of intrinsic immune actions, and the efficacy of these effects is strictly associated with the appearance of hypoxia, necrosis, and inflammation at the tumor sites [3]. These biological processes can affect the immune system and adjust antitumor responses, giving rise to atypical responses, including pseudoprogression (PsP) and hyperprogression disease (HPD) [4,5,6,7]. The identification of a reliable predictive biomarker of atypical responses to immunotherapy across various solid tumors remains an unmet need in clinic practice so far
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have