Abstract 136P
Background
Intrinsic links of variation in immune function and phases of circadian rhythm is the basis of chronotherapy. Modulating immune potentiating nature of modern anti-cancer treatment combinations such as PDL1 inhibitors, Stereotactic body radiotherapy (SBRT), stromal targeted theranostic using chronobiology is an unfathomed area of research. SBRT releases tumour neo-antigens, the anti PDL1 therapy aids in effective cytotoxic T cell activity and anti-stromal theranostic modulates the resistant tumour stroma with an anti TGF Beta activity in an immune favouring way. Chrono-phased SBRT -Timing the SBRT at the best immune functioning part of the day could be an effective synergism to the amalgam.
Methods
26 disseminated cancer patients eligible for anti-PDL1 drug were treated with Actinium-225 tagged fibroblast activated protein (FAP) based Alpha theranostic to target the cancer associated fibroblasts (CAFs) forming the tumor stroma and were randomized to receive SBRT at any given part of the day versus a chrono-phased SBRT-7am to 9am after verifying the circadian rhythm.Intactness of the circadian rhythm in these patients were assessed using sleep log. Baseline cytokine profile, WBC, ALC and NL ratio were compared to immediate therapy level and post 3-months. Response to therapy was radiologically assessed using RECIST 1.1 criteria.
Results
Table: 136P
Response | Regular SBRT (13 cases) | Chrono-SBRT (13 cases) |
Partial (PR) | 3 | 4 |
Complete (CR) | 0 | 1 |
Progression (PD) | 2 | 1 |
Mixed Type-1 (PR+CR) | 3 | 5 |
Mixed Type-2 (PD+PR) | 5 | 2 |
Conclusions
While augmenting immune responses to cancer immune-modulatory therapies is an area of active probing, using the immune sensitive phase of circadian rhythm to obtain therapeutic benefit seams beneficial. Our study suggests that the technique is feasible, and our early results are encouraging with better quality of life with chrono-sbrt.
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
78P - Final Analysis of the French Real-World Study EVIDENS: Effectiveness, Safety & Quality of Life At 36 Months of Nivolumab in Advanced Non-Small Cell Lung Cancer (NSCLC)
Presenter: Fabrice Barlesi
Session: Poster Display
79P - A prospective, single-arm, phase II study to evaluate the efficacy and safety of Tislelizumab plus chemotherapy in resectable NSCLC
Presenter: Daqiang Sun
Session: Poster Display
80P - Efficacy and Safety of Tislelizumab Combined with Anlotinib and 2-cycles Chemotherapy as First-line Treatment for Advanced NSCLC(TISAL-FE-01)
Presenter: jun Tang
Session: Poster Display
81P - Real-World Experience with Docetaxel Regimens in Metastatic Non-Squamous (mNSq) Non-Small Cell Lung Cancer (NSCLC) Patients Previously Treated with Platinum-Based Chemotherapy (PCT) and an Immune Checkpoint Inhibitor (ICI) in the United States (US)
Presenter: Marisa Bittoni
Session: Poster Display
82P - The Role of Circadian Rhythms in NSCLC Immunotherapy Efficacy: A Focus on First Dose Timing
Presenter: Martin Igor Gomez-Randulfe Rodriguez
Session: Poster Display
84P - Adebrelimab plus chemotherapy (chemo) as first-line treatment for extensive-stage small-cell lung cancer (ES-SCLC): 3-year update of the phase 3 CAPSTONE-1 study
Presenter: Ying Cheng
Session: Poster Display
85P - Phase II trial of tislelizumab plus sitravatinib as maintenance therapy in extensive-stage small-cell lung cancer (ES-SCLC)
Presenter: Yun Fan
Session: Poster Display
86P - Durvalumab plus Olaparib as maintenance therapy in extensive-stage small-cell lung cancer (TRIDENT): updated efficacy and safety analysis
Presenter: Yan Huang
Session: Poster Display
88P - Adverse events (AEs) as potential predictive factors of activity in patients with advanced hepatocellular carcinoma (HCC) treated with atezolizumab plus bevacizumab (AB)
Presenter: MARA PERSANO
Session: Poster Display