Abstract 82P
Background
Circadian rhythms are known to influence adaptive immune responses. A seminal study showed that immune checkpoint inhibitors (ICI) infusions administered in the evening (later than 16:30h) to stage IV melanoma patients led to significantly shorter progression-free survival (PFS) and overall survival (OS). Subsequent retrospective studies suggested worse outcomes for metastatic non-small cell lung cancer (NSCLC) patients who received over 20% of their ICI doses in the evening. We hypothesized that the timing of the initial dose could be responsible for this observed effect.
Methods
We conducted a retrospective review of patients diagnosed with advanced or metastatic NSCLC who initiated palliative first line pembrolizumab treatment between June 2017 and April 2023 at The Christie. Sociodemographic and clinical data were collected. Patients were stratified into two groups based on the timing of their first dose infusion: those before 16:30h (early group) and those after 16:30h (evening group).
Results
276 patients met the inclusion criteria: 237 in the early group and 39 in the evening group. Both cohorts were similar, with no significant differences in sex, ECOG, histology, brain metastases at diagnosis, or PD-L1 expression (≥ or <90%). Inflammatory blood biomarkers (NLR, PLR, PNI) were consistent between groups. The evening group had a significantly shorter median OS (16m vs. 19m; HR 1.5; p=0.047), corroborated by the multivariate analysis (Table). Although median PFS was comparable between groups, the 3-year PFS rates stood at 10% for the evening group and 22% for the early group. Table: 82P
Multivariate Cox regression model
HR (95%) | P | |
ECOG PS | 0.50 (0.26 - 0.94) | 0.031 |
Histology (non-squamous) | 0.76 (0.55 - 1.04) | 0.083 |
PD-L1 <90% | 1.58 (1.17 - 2.15) | 0.003 |
NLR <5 | 0.61 (0.45 - 0.82) | 0.001 |
Evening Group | 1.63 (1.09 - 2.43) | 0.018 |
Conclusions
Our findings add to the emerging body of evidence suggesting a link between circadian rhythms and immunotherapy efficacy. While this study indicates a difference in OS based on the timing of the first dose, further prospective research is imperative. Modifying infusion timings could provide a straightforward approach to potentially optimizing patient outcomes.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
F. Blackhall: Financial Interests, Personal, Invited Speaker, Educational Symposium lecture: AstraZeneca; Financial Interests, Personal, Advisory Board, NTRK Advisory Board and guidelines for diagnosis: Bayer; Financial Interests, Personal, Other, IDMC Chair: AstraZeneca; Financial Interests, Personal, Advisory Board, Small cell Advisory Board Oct 2020: Amgen; Financial Interests, Personal, Invited Speaker, ESMO Satellite Symposium November 2020: Takeda; Financial Interests, Personal, Other, Consultancy for RETinhibitor development: Blueprint; Financial Interests, Personal, Other, Real world evidence research study design and analysis (EGFR): Janssen; Financial Interests, Institutional, Coordinating PI, Institutional payment for clinical trial activities: Amgen, Pfizer; Financial Interests, Institutional, Coordinating PI, Payment for clinical trial activities: Mirati; Financial Interests, Institutional, Coordinating PI, Clinical trial activities: BMS; Financial Interests, Institutional, Funding, Real world evidence research programme: Roche; Non-Financial Interests, Personal, Advisory Role, Application of genotyping platforms in lung cancer: Guardant Health; Non-Financial Interests, Personal, Advisory Role, Clinical trials of IMPs in lung cancer and translational lung cancer biomarkers: AstraZeneca. R. Califano: Financial Interests, Personal, Advisory Board: AstraZeneca, Bayer, Lilly Oncology, Roche, Pfizer, MSD, Takeda, Amgen, Bayer, Janssen and Novartis, Sanofi, GSK and PharmaMar; Financial Interests, Personal, Invited Speaker: AstraZeneca, Lilly Oncology, Roche, Pfizer, MSD, Takeda, Amgen, GSK and Janssen; Financial Interests, Personal, Other, speaker in educational activities: Medscape, Touch IME and PeerVoice; Financial Interests, Personal, Ownership Interest, partnership: The Christie Private Care - LOC; Financial Interests, Personal, Stocks/Shares: Supportive care UK; Financial Interests, Institutional, Local PI, principal investigator for clinical trial: Roche, AstraZeneca, Pfizer, Clovis, Lilly Oncology, MSD, BMS, AbbVie, Takeda, Janssen, and Novartis; Financial Interests, Institutional, Local PI: PharmaMar and GSK; Non-Financial Interests, Personal, Member, member of Lung Cancer Group: EORTC. All other 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
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