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
1014P - Phase Ib trial results of safety, pharmacokinetics and pharmacodynamics of TU2218, TGFβ-RI and VEGF-R2 dual inhibitor in combination with pembrolizumab in patients with advanced solid tumors
Presenter: Anthony Tolcher
Session: Poster session 03
1015P - The efficacy and mechanism of pan-FGFR inhibitor (AZD4547) combined with immunoagonists or immunosuppressants in FGFR-positive tumors
Presenter: Qizhi Ma
Session: Poster session 03
1016P - Phase I study of SOF10 plus atezolizumab in patients with advanced/recurrent solid tumours
Presenter: Toshihiko Doi
Session: Poster session 03
1017P - Updated safety and efficacy from the phase I study of givastomig, a novel claudin 18.2/4-1BB bispecific antibody, in claudin 18.2 positive advanced gastroesophageal carcinoma (GEC)
Presenter: Samuel Klempner
Session: Poster session 03
1018P - Leveraging innate and adaptive immunity with AFM24 and atezolizumab in metastatic gastric cancer
Presenter: Omar Saavedra Santa Gadea
Session: Poster session 03
1019P - Bispecific PD1-IL2 antibody reshapes the inhibitory immune microenvironment of SMARCA4 mutant non-small cell lung cancer by reversing CD8+T cell exhaustion
Presenter: Bo Cheng
Session: Poster session 03
Resources:
Abstract
1020P - Highly potent and specific bivalent T cell engager (TCE) targeting PRAME on HLA-A*02:01
Presenter: Athanasia Dasargyri
Session: Poster session 03
1021P - Chemotherapy and hypomethylating agents enhance anti-tumor activity of PRAME ImmTAC
Presenter: Adel Benlahrech
Session: Poster session 03
1022P - A phase II trial of the IO102-IO103 vaccine plus pembrolizumab: Completed cohort for first-line (1L) treatment of advanced squamous cell carcinoma of the head and neck (SCCHN)
Presenter: Jonathan Riess
Session: Poster session 03
1023P - Long-term follow up of patients treated with a DNA vaccine (pTVG-HP) for PSA-recurrent prostate cancer
Presenter: Douglas McNeel
Session: Poster session 03