Abstract 1060P
Background
For cancer neoadjuvant and adjuvant immunotherapy, after several decades of evolution, the field currently possesses an enormous volume of underutilized data. Informatics analysis to thoroughly excavate the similarities and differences between the two is desperately necessary.
Methods
Extensive relevant studies (n=1373) on neoadjuvant and adjuvant immunotherapy from 2014-2023 were collected for quantitative, hierarchical clustering, and comparative analyses after vigorous quality control.
Results
Over the last decade, neoadjuvant and adjuvant immunotherapy enjoyed promising development status (Annual Growth Rate: 25.18% vs 6.52%) and global collaboration (International Co-authorships: 19.93% vs 19.84%). Unsupervised hierarchical clustering identified their dominant research clusters, in which Cluster 4: Balance of neoadjuvant immunotherapy efficacy and safety and Cluster 2: Adjuvant immunotherapy clinical trials are emerging research populations. Burst and regression curve analyses uncovered domain pivotal research signatures, including biomarkers (R2=0.6505, p=0.0086) in neoadjuvant scenarios, and tumor microenvironment (R2=0.5571, p=0.0209) in adjuvant scenarios. The Walktrap algorithm further revealed that "non-small cell lung cancer, immune checkpoint inhibitors, melanoma" and "melanoma, hepatocellular carcinoma, dendritic cells" (Relevance Percentage: 100% vs 100%, Development Percentage: 37.5% vs 17.1%) are extensively relevant to this field, but remain underdeveloped. Furthermore, comprehensive quantitative comparisons revealed that this field's spotlight on neoadjuvant immunotherapy overtook adjuvant immunotherapy entirely after 2020; such a qualitative finding will facilitate proper decision-making for subsequent research and avoid significant wastage of healthcare resources.
Conclusions
This cross-sectional study comparatively analyzed the fundamental metrological information in cancer neoadjuvant and adjuvant immunotherapy, identified their pivotal research signatures, and provided some substantial predictions for their subsequent preclinical and clinical research.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1003P - A first-in-human (FIH) phase I study of IPH5301, an anti-CD73 monoclonal antibody (mAb), in patients with advanced solid tumors (AST) (CHANCES, NCT05143970)
Presenter: Mathilde Beaufils
Session: Poster session 03
1004P - Phase I/II trial of ASP1570, a novel diacylglycerol kinase ζ inhibitor, in patients with advanced solid tumors
Presenter: Daniel Olson
Session: Poster session 03
1005P - Microbial ecosystem therapeutics 4 (MET4) treatment mediates a humoral response in patients treated with immune checkpoint inhibition (ICI)
Presenter: Pavlina Spiliopoulou
Session: Poster session 03
1007P - Systemic STING agonist BI 1703880 plus ezabenlimab in patients (pts) with advanced solid tumors: Initial results from a phase Ia study
Presenter: Kevin Harrington
Session: Poster session 03
1008P - Preliminary clinical PK and PD analysis of a phase I study of ZL-1218, a humanized anti-CCR8 IgG1 antibody, in patients with advanced solid tumors
Presenter: Ignacio Gil Bazo
Session: Poster session 03
1010P - Phase I dose-escalation study of HBM1020: A novel anti-B7H7 antibody in patients with advanced solid tumors
Presenter: Jason Henry
Session: Poster session 03
1011P - Model-informed dose optimization of HFB200301, a TNFR2 agonist monoclonal antibody (mAb), in monotherapy and in combination with the anti-PD-1 mAb tislelizumab (TIS), in patients (pts) with advanced solid tumors
Presenter: Desamparados Roda Perez
Session: Poster session 03
1012P - Safety, tolerability, and efficacy of nadunolimab in combination with pembrolizumab in patients with solid tumors
Presenter: roger cohen
Session: Poster session 03
1013P - A phase I study of rivoceranib combined with nivolumab in patients with unresectable or metastatic cancer
Presenter: Neal Chawla
Session: Poster session 03