Abstract 503P
Background
Circadian fluctuations in T-cell function may modulate the efficacy of immune checkpoint inhibitors (ICIs). An association between time-of-day of ICI infusion and outcomes in patients with advanced non-small cell lung cancer (NSCLC) and melanoma has been reported; however, such association in patients with locally advanced NSCLC remains unclear. We aimed to determine whether durvalumab time-of-day infusion could impact the survival of patients with locally advanced NSCLC.
Methods
We retrospectively analyzed patients with unresectable locally advanced NSCLC treated with chemoradiation and adjuvant durvalumab between January 2018 and May 2022. According to previous research, the receipt of ≥20% vs <20% of infusions after the 15:00h cut-off time was set as the threshold for analysis. We calculated the association between the proportion of durvalumab infusions after 15:00h and survival (PFS [progression-free survival] and OS [overall survival]) using Cox regression.
Results
82 patients were included. The median age was 69 years (IQR, 44–85), 67 patients (82%) were male, 78 (95%) were current or former tobacco smokers, and 79 (96%) had performance status (PS) 0 or 1. Histology was non-squamous for 49 (60%). PD-L1 expression <50% was for 36 (44%). Patients who received at least 20% of durvalumab infusions after 15:00h (12 out of 82, 15%) vs. less than 20% of durvalumab infusions (70 out of 82, 85%) had a statistically significant shorter PFS (median 6.4 months vs not reached, HR: 0.36 [95% CI: 0.16–0.80], P = 0.011) and a trend of shorter OS (median 20.4 months vs not reached, HR: 0.36 [95% CI: 0.21–1.23], P = 0.16). In the multivariate analysis, patients who received at least 20% of durvalumab infusions after 15:00h vs. less than 20% of durvalumab infusions had a statistically significant shorter PFS (HR: 0.38 [95% CI: 0.17–0.88], P = 0.023) and OS (HR: 0.41 [95% CI: 0.16–0.98], P = 0.048).
Conclusions
Time-of-day infusion of durvalumab may impact the survival of patients with locally advanced NSCLC. Although prospective studies of the timing of ICIs are needed, efforts towards scheduling infusions before mid-afternoon might be beneficial.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The author.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
602P - COLUMBUS 7-year update: A randomized, open-label, phase III trial of encorafenib (Enco) + binimetinib (Bini) vs vemurafenib (Vemu) or Enco in patients (Pts) with BRAF V600-mutant melanoma
Presenter: Andrew Haydon
Session: Poster Display
Resources:
Abstract
603P - An individualised postoperative radiological surveillance schedule for IDH-wildtype glioblastoma patients (HK-GBM Registry)
Presenter: Jason Chak Yan Li
Session: Poster Display
Resources:
Abstract
604P - Cabozantinib versus placebo in patients with radioiodine-refractory differentiated thyroid cancer who progressed after prior VEGFR-targeted therapy: Outcomes from COSMIC-311 by BRAF status
Presenter: Marcia Brose
Session: Poster Display
Resources:
Abstract
606P - BRAF and NRAS mutations are associated with poor prognosis in Asians with acral-lentiginous and nodular cutaneous melanoma
Presenter: Sumadi Lukman Anwar
Session: Poster Display
Resources:
Abstract
607P - Single institutional outcomes of radiotherapy and systemic therapy for melanoma brain metastases in Japan
Presenter: Naoya Yamazaki
Session: Poster Display
Resources:
Abstract
608P - The efficacy of immune checkpoint inhibitors and targeted therapy in mucosal melanomas: A systematic review and meta-analysis
Presenter: Andrea Teo
Session: Poster Display
Resources:
Abstract
609P - The association between thyroid function abnormalities and vitiligo induced by pembrolizumab regarding prognosis in patients with advanced melanoma
Presenter: Moez Mobarek
Session: Poster Display
Resources:
Abstract
610P - Analyzing the clinical benefit of the evidence presented at these congresses and utilizing a standardized scale to quantify it will significantly enhance our understanding of the studies showcased, allowing for more objective evaluation and interpretation
Presenter: Charles Jeffrey Tan
Session: Poster Display
Resources:
Abstract
611P - ESMO-magnitude of clinical benefit scale (MCBS) scores for phase III trials of adjuvant and curative therapies at the 2022 ASCO annual meeting (ASCO22)
Presenter: Thi Thao Vi Luong
Session: Poster Display
Resources:
Abstract
612P - Is the juice worth the squeeze? Overall survival gain per unit treatment time as a metric of clinical benefit of systemic treatment in incurable cancers
Presenter: Vodathi Bamunuarachchi
Session: Poster Display
Resources:
Abstract